Molecules for disease detection and treatment

Abstract
The present invention provides purified disease detection and treatment molecule polynucleotides (mddt). Also encompassed are the polypeptides (MDDT) encoded by mddt. The invention also provides for the use of mddt, or complements, oligonucleotides, or fragments thereof in diagnostic assays. The invention further provides for vectors and host cells containing mddt for the expression of MDDT. The invention additionally provides for the use of isolated and purified MDDT to induce antibodies and to screen libraries of compounds and the use of anti-MDDT antibodies in diagnostic assays. Also provided are microarrays containing mddt and methods of use.
Description


TECHNICAL FIELD

[0001] The present invention relates to molecules for disease detection and treatment and to the use of these sequences in the diagnosis, study, prevention, and treatment of diseases associated with, as well as effects of exogenous compounds on, the expression of molecules for disease detection and treatment.



BACKGROUND OF THE INVENTION

[0002] The human genome is comprised of thousands of genes, many encoding gene products that function in the maintenance and growth of the various cells and tissues in the body. Aberrant expression or mutations in these genes and their products is the cause of, or is associated with, a variety of human diseases such as cancer and other cell proliferative disorders. The identification of these genes and their products is the basis of an ever-expanding effort to find markers for early detection of diseases, and targets for their prevention and treatment.


[0003] For example, cancer represents a type of cell proliferative disorder that affects nearly every tissue in the body. A wide variety of molecules, either aberrantly expressed or mutated, can be the cause of, or involved with, various cancers because tissue growth involves complex and ordered patterns of cell proliferation, cell differentiation, and apoptosis. Cell proliferation must be regulated to maintain both the number of cells and their spatial organization. This regulation depends upon the appropriate expression of proteins which control cell cycle progression in response to extracellular signals such as growth factors and other mitogens, and intracellular cues such as DNA damage or nutrient starvation. Molecules which directly or indirectly modulate cell cycle progression fall into several categories, including growth factors and their receptors, second messenger and signal transduction proteins, oncogene products, tumor-suppressor proteins, and mitosis-promoting factors. Aberrant expression or mutations in any of these gene products can result in cell proliferative disorders such as cancer. Oncogenes are genes generally derived from normal genes that, through abnormal expression or mutation, can effect the transformation of a normal cell to a malignant one (oncogenesis). Oncoproteins, encoded by oncogenes, can affect cell proliferation in a variety of ways and include growth factors, growth factor receptors, intracellular signal transducers, nuclear transcription factors, and cell-cycle control proteins. In contrast, tumor-suppressor genes are involved in inhibiting cell proliferation. Mutations which cause reduced or loss of function in tumor-suppressor genes result in aberrant cell proliferation and cancer. Thus a wide variety of genes and their products have been found that are associated with cell proliferative disorders such as cancer, but many more may exist that are yet to be discovered.


[0004] DNA-based arrays can provide a simple way to explore the expression of a single polymorphic gene or a large number of genes. When the expression of a single gene is explored, DNA-based arrays are employed to detect the expression of specific gene variants. For example, a p53 tumor suppressor gene array is used to determine whether individuals are carrying mutations that predispose them to cancer. A cytochrome p450 gene array is useful to determine whether individuals have one of a number of specific mutations that could result in increased drug metabolism, drug resistance or drug toxicity.


[0005] DNA-based array technology is especially relevant for the rapid screening of expression of a large number of genes. There is a growing awareness that gene expression is affected in a global fashion. A genetic predisposition, disease or therapeutic treatment may affect, directly or indirectly, the expression of a large number of genes. In some cases the interactions may be expected, such as when the genes are part of the same signaling pathway. In other cases, such as when the genes participate in separate signaling pathways, the interactions may be totally unexpected. Therefore, DNA-based arrays can be used to investigate how genetic predisposition, disease, or therapeutic treatment affects the expression of a large number of genes.


[0006] The discovery of new molecules for disease detection and treatment satisfies a need in the art by providing new compositions which are useful in the diagnosis, study, prevention, and treatment of diseases associated with, as well as effects of exogenous compounds on, the expression of molecules for disease detection and treatment.



SUMMARY OF THE INVENTION

[0007] The present invention relates to human disease detection and treatment molecule polynucleotides (mddt) as presented in the Sequence Listing. The mddt uniquely identify genes encoding structural, functional, and regulatory disease detection and treatment molecules.


[0008] The invention provides an isolated polynucleotide selected from the group consisting of a) a polynucleotide comprising a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-252; b) a polynucleotide comprising a naturally occurring polynucleotide sequence at least 90% identical to a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-252; c) a polynucleotide complementary to the polynucleotide of a); d) a polynucleotide complementary to the polynucleotide of b); and e) an RNA equivalent of a) through d). In one alternative, the polynucleotide comprises a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-252. In another alternative, the polynucleotide comprises at least 30 contiguous nucleotides of a polynucleotide selected from the group consisting of a) a polynucleotide comprising a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-252; b) a polynucleotide comprising a naturally occurring polynucleotide comprising a polynucleotide sequence at lease identical to a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-252; c) a polynucleotide complementary to the polynucleotide of a); d) a polynucleotide complementary to the polynucleotide of b); and e) an RNA equivalent of a) through d). In another alternative, the polynucleotide comprises at least 60 contiguous nucleotides of a polynucleotide selected from the group consisting of a) a polynucleotide comprising a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-252; b) a polynucleotide comprising a naturally occurring polynucleotide comprising a polynucleotide sequence at least 90% identical to a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-252; c) a polynucleotide complementary to the polynucleotide of a); d) a polynucleotide complementary to the polynucleotide of b); and e) an RNA equivalent of a) through d). The invention further provides a composition for the detection of expression of disease detection and treatment molecule polynucleotides comprising at least one isolated polynucleotide comprising a polynucleotide selected from the group consisting of a) a polynucleotide comprising a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-252; b) a polynucleotide comprising a naturally occurring polynucleotide sequence at least 90% identical to a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-252; c) a polynucleotide complementary to the polynucleotide of a); d) a polynucleotide complementary to the polynucleotide of b); and e) an RNA equivalent of a) through d); and a detectable label.


[0009] The invention also provides a method for detecting a target polynucleotide in a sample, said target polynucleotide having a polynucleotide sequence of a polynucleotide selected from the group consisting of a) a polynucleotide comprising a polynucleotide sequence of a polynucleotide selected from the group consisting of SEQ ID NO:1-252; b) a polynucleotide comprising a naturally occurring polynucleotide sequence at least 90% identical to a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-252; c) a polynucleotide complementary to the polynucleotide of a); d) a polynucleotide complementary to the polynucleotide of b); and e) an RNA equivalent of a) through d). The method comprises a) amplifying said target polynucleotide or fragment thereof using polymerase chain reaction amplification, and b) detecting the presence or absence of said amplified target polynucleotide or fragment thereof, and, optionally, if present, the amount thereof.


[0010] The invention also provides a method for detecting a target polynucleotide in a sample, said target polynucleotide having a polynucleotide selected from the group consisting of a) a polynucleotide comprising a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-252; b) a polynucleotide comprising a naturally occurring polynucleotide sequence at least 90% identical to a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-252; c) a polynucleotide complementary to the polynucleotide of a); d) a polynucleotide complementary to the polynucleotide of b); and e) an RNA equivalent of a) through d). The method comprises a) hybridizing the sample with a probe comprising at least 60 contiguous nucleotides comprising a sequence complementary to said target polynucleotide in sample, and which probe specifically hybridizes to said target polynucleotide, under conditions whereby a hybridization complex is formed between said probe and said target polynucleotide, and b) detecting the presence or absence of said hybridization complex, and, optionally, if present, the amount thereof. In one alternative, the invention provides a composition comprising a target polynucleotide of the method, wherein said probe comprises at least 30 contiguous nucleotides. In one alternative, the invention provides a composition comprising a target polynucleotide of the method, wherein said probe comprises at least 60 contiguous nucleotides.


[0011] The invention further provides a recombinant polynucleotide comprising a promoter sequence operably linked to an isolated polynucleotide selected from the group consisting of a) a polynucleotide comprising a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-252; b) a polynucleotide comprising a naturally occurring polynucleotide sequence at least 90% identical to a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-252; c) a polynucleotide complementary to the polynucleotide of a); d) a polynucleotide complementary to the polynucleotide of b); and e) an RNA equivalent of a) through d). In one alternative, the invention provides a cell transformed with the recombinant polynucleotide. In another alternative, the invention provides a transgenic organism comprising the recombinant polynucleotide.


[0012] The invention also provides a method for producing a disease detection and treatment polypeptide, the method comprising a) culturing a cell under conditions suitable for expression of the disease detection and treatment polypeptide, wherein said cell is transformed with a recombinant polynucleotide, said recombinant polynucleotide comprising an isolated polynucleotide selected from the group consisting of i) a polynucleotide comprising a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-252; ii) a polynucleotide comprising a naturally occurring polynucleotide sequence at least 90% identical to a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-252; iii) a polynucleotide complementary to the polynucleotide of i); iv) a polynucleotide complementary to the polynucleotide of ii); and v) an RNA equivalent of i) through iv), and b) recovering the disease detection and treatment polypeptide so expressed. The invention additionally provides a method wherein the polypeptide has an amino acid sequence selected from the group consisting of SEQ ID NO:253-506.


[0013] The invention also provides an isolated disease detection and treatment polypeptide (MDDT) encoded by at least one polynucleotide comprising a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-252. The invention further provides a method of screening for a test compound that specifically binds to the polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506. The method comprises a) combining the polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506 with at least one test compound under suitable conditions, and b) detecting binding of the polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506 to the test compound, thereby identifying a compound that specifically binds to the polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506.


[0014] The invention further provides a microarray wherein at least one element of the microarray is an isolated polynucleotide comprising at least 30 contiguous nucleotides of a polynucleotide selected from the group consisting of a) a polynucleotide comprising a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-252; b) a polynucleotide comprising a naturally occurring polynucleotide sequence at least 90% identical to a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-252; c) a polynucleotide complementary to the polynucleotide of a); d) a polynucleotide complementary to the polynucleotide of b); and e) an RNA equivalent of a) through d). The invention also provides a method for generating a transcript image of a sample which contains polynucleotides. The method comprises a) labeling the polynucleotides of the sample, b) contacting the elements of the microarray with the labeled polynucleotides of the sample under conditions suitable for the formation of a hybridization complex, and c) quantifying the expression of the polynucleotides in the sample.


[0015] Additionally, the invention provides a method for screening a compound for effectiveness in altering expression of a target polynucleotide, wherein said target polynucleotide comprises a polynucleotide selected from the group consisting of a) a polynucleotide comprising a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-252; b) a polynucleotide comprising a naturally occurring polynucleotide sequence at least 90% identical to a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-252; c) a polynucleotide complementary to the polynucleotide of a); d) a polynucleotide complementary to the polynucleotide of b); and e) an RNA equivalent of a) through d). The method comprises a) exposing a sample comprising the target polynucleotide to a compound, b) detecting altered expression of the target polynucleotide, and c) comparing the expression of the target polynucleotide in the presence of varying amounts of the compound and in the absence of the compound.


[0016] The invention further provides a method for assessing toxicity of a test compound, said method comprising a) treating a biological sample containing nucleic acids with the test compound; b) hybridizing the nucleic acids of the treated biological sample with a probe comprising at least 20 contiguous nucleotides of a polynucleotide selected from the group consisting of i) a polynucleotide comprising a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-252; ii) a polynucleotide comprising a naturally occurring polynucleotide sequence at least 90% identical to a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-252; iii) a polynucleotide complementary to the polynucleotide of i); iv) a polynucleotide complementary to the polynucleotide of ii); and v) an RNA equivalent of i) through iv). Hybridization occurs under conditions whereby a specific hybridization complex is formed between said probe and a target polynucleotide in the biological sample, said target polynucleotide comprising a polynucleotide sequence of a polynucleotide selected from the group consisting of i) a polynucleotide comprising a polynucleotide sequence selected from the group consisting of SEQ ID NO:11-252; ii) a polynucleotide comprising a naturally occurring polynucleotide sequence at least 90% identical to a polynucleotide sequence selected from the group consisting of SEQ ID NO:11-252; iii) a polynucleotide complementary to the polynucleotide of i); iv) a polynucleotide complementary to the polynucleotide of ii); and v) an RNA equivalent of i) through iv), and alternatively, the target polynucleotide comprises a polynucleotide sequence of a fragment of a polynucleotide selected from the group consisting of i-v above; c) quantifying the amount of hybridization complex; and d) comparing the amount of hybridization complex in the treated biological sample with the amount of hybridization complex in an untreated biological sample, wherein a difference in the amount of hybridization complex in the treated biological sample is indicative of toxicity of the test compound.


[0017] The invention further provides an isolated polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:253-506, b) a polypeptide comprising a naturally occurring amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO:253-506, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506. In one alternative, the invention provides an isolated polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:253-506.


[0018] The invention further provides an isolated polynucleotide encoding a polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:253-506, b) a polypeptide comprising a naturally occurring amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO:253-506, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506. In one alternative, the polynucleotide encodes a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:253-506. In another alternative, the polynucleotide comprises a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-252.


[0019] Additionally, the invention provides an isolated antibody which specifically binds to a polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:253-506, b) a polypeptide comprising a naturally occurring amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO:253-506, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506.


[0020] The invention further provides a composition comprising a polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:253-506, b) a polypeptide comprising a naturally occurring amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO:253-506, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506, and a pharmaceutically acceptable excipient. In one embodiment, the composition comprises a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506. The invention additionally provides a method of treating a disease or condition associated with decreased expression of functional MDDT, comprising administering to a patient in need of such treatment the composition.


[0021] The invention also provides a method for screening a compound for effectiveness as an agonist of a polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:253-506, b) a polypeptide comprising a naturally occurring amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO:253-506, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506. The method comprises a) exposing a sample comprising the polypeptide to a compound, and b) detecting agonist activity in the sample. In one alternative, the invention provides a composition comprising an agonist compound identified by the method and a pharmaceutically acceptable excipient. In another alternative, the invention provides a method of treating a disease or condition associated with decreased expression of functional MDDT, comprising administering to a patient in need of such treatment the composition.


[0022] Additionally, the invention provides a method for screening a compound for effectiveness as an antagonist of a polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:253-506, b) a polypeptide comprising a naturally occurring amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO:253-506, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506. The method comprises a) exposing a sample comprising the polypeptide to a compound, and b) detecting antagonist activity in the sample. In one alternative, the invention provides a composition comprising an antagonist compound identified by the method and a pharmaceutically acceptable excipient. In another alternative, the invention provides a method of treating a disease or condition associated with overexpression of functional MDDT, comprising administering to a patient in need of such treatment the composition.


[0023] The invention further provides a method of screening for a compound that modulates the activity of a polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:253-506, b) a polypeptide comprising a naturally occurring amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO:253-506, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506. The method comprises a) combining the polypeptide with at least one test compound under conditions permissive for the activity of the polypeptide. b) assessing the activity of the polypeptide in the presence of the test compound, and c) comparing the activity of the polypeptide in the presence of the test compound with the activity of the polypeptide in the absence of the test compound, wherein a change in the activity of the polypeptide in the presence of the test compound is indicative of a compound that modulates the activity of the polypeptide.



DESCRIPTION OF THE TABLES

[0024] Table 1 shows the sequence identification numbers (SEQ ID NO:s) and template identification numbers (template IDs) corresponding to the polynucleotides of the present invention, along with the sequence identification numbers (SEQ ID NO:s) and open reading frame identification numbers (ORF IDs) corresponding to polypeptides encoded by the template ID.


[0025] Table 2 shows the sequence identification numbers (SEQ ID NO:s) and template identification numbers (template IDs) corresponding to the polynucleotides of the present invention, along with their GenBank hits (GI Numbers), probability scores, and functional annotations corresponding to the GenBank hits.


[0026] Table 3 shows the sequence identification numbers (SEQ ID NO:s) and template identification numbers (template IDs) corresponding to the polynucleotides of the present invention, along with polynucleotide segments of each template sequence as defined by the indicated “start” and “stop” nucleotide positions. The reading frames of the polynucleotide segments and the Pfam hits. Pfam descriptions, and E-values corresponding to the polypeptide domains encoded by the polynucleotide segments are indicated.


[0027] Table 4 shows the sequence identification numbers (SEQ ID NO:s) and template identification numbers (template IDs) corresponding to the polynucleotides of the present invention, along with polynucleotide segments of each template sequence as defined by the indicated “start” and “stop” nucleotide positions. The reading frames of the polynucleotide segments are shown, and the polypeptides encoded by the polynucleotide segments constitute either signal peptide (SP) or transmembrane (TM) domains, as indicated. The membrane topology of the encoded polypeptide sequence is indicated, the N-terminus (N) listed as being oriented to either the cytosolic (N in) or non-cytosolic (N out) side of the cell membrane or organelle.


[0028] Table 5 shows the sequence identification numbers (SEQ ID NO:s) and template identification numbers (template IDs) corresponding to the polynucleotides of the present invention, along with component sequence identification numbers (component IDs) corresponding to each template. The component sequences, which were used to assemble the template sequences, are defined by the indicated “start” and “stop” nucleotide positions along each template.


[0029] Table 6 shows the tissue distribution profiles for the templates of the invention.


[0030] Table 7 shows the sequence identification numbers (SEQ ID NO:s) corresponding to the polypeptides of the present invention, along with the reading frames used to obtain the polypeptide segments, the lengths of the polypeptide segments, the “start” and “stop” nucleotide positions of the polynucleotide sequences used to define the encoded polypeptide segments, the GenBank hits (GI Numbers), probability scores, and functional annotations corresponding to the GenBank hits.


[0031] Table 8 summarizes the bioinformatics tools which are useful for analysis of the polynucleotides of the present invention. The first column of Table 8 lists analytical tools, programs, and algorithms, the second column provides brief descriptions thereof, the third column presents appropriate references, all of which are incorporated by reference herein in their entirety, and the fourth column presents, where applicable, the scores, probability values, and other parameters used to evaluate the strength of a match between two sequences (the higher the score, the greater the homology between two sequences).







DETAILED DESCRIPTION OF THE INVENTION

[0032] Before the nucleic acid sequences and methods are presented, it is to be understood that this invention is not limited to the particular machines, methods, and materials described. Although particular embodiments are described, machines, methods, and materials similar or equivalent to these embodiments may be used to practice the invention. The preferred makes, methods, and materials set forth are not intended to limit the scope of the invention which is limited only by the appended claims.


[0033] The singular forms “a”, “an”, and “the” include plural reference unless the context clearly dictates otherwise. All technical and scientific terms have the meanings commonly understood by one of ordinary skill in the art. All publications are incorporated by reference for the purpose of describing and disclosing the cell lines, vectors, and methodologies which are presented and which might be used in connection with the invention. Nothing in the specification is to be construed as an admission that the invention is not entitled to antedate such disclosure by virtue of prior invention.


[0034] Definitions


[0035] As used herein, the lower case “mddt” refers to a nucleic acid sequence, while the upper case “MDDT” refers to an amino acid sequence encoded by mddt. A “full-length” mddt refers to a nucleic acid sequence containing the entire coding region of a gene endogenously expressed in human tissue.


[0036] “Adjuvants” are materials such as Freund's adjuvant, mineral gels (aluminum hydroxide), and surface active substances (lysolecithin, pluronic polyols, polyanions, peptides, oil emulsions, keyhole limpet hemocyanin, and dinitrophenol) which may be administered to increase a host's immunological response.


[0037] “Allele” refers to an alternative form of a nucleic acid sequence. Alleles result from a “mutation,” a change or an alternative reading of the genetic code. Any given gene may have none, one, or many allelic forms. Mutations which give rise to alleles include deletions, additions, or substitutions of nucleotides. Each of these changes may occur alone, or in combination with the others, one or more times in a given nucleic acid sequence. The present invention encompasses allelic mddt.


[0038] “Amino acid sequence” refers to a peptide, a polypeptide, or a protein of either natural or synthetic origin. The amino acid sequence is not limited to the complete, endogenous amino acid sequence and may be a fragment, epitope, variant, or derivative of a protein expressed by a nucleic acid sequence.


[0039] “Amplification” refers to the production of additional copies of a sequence and is carried out using polymerase chain reaction (PCR) technologies well known in the art.


[0040] “Antibody” refers to intact molecules as well as to fragments thereof, such as Fab, F(ab′)2, and Fv fragments, which are capable of binding the epitopic determinant. Antibodies that bind MDDT polypeptides can be prepared using intact polypeptides or using fragments containing small peptides of interest as the immunizing antigen. The polypeptide or peptide used to immunize an animal (e.g., a mouse, a rat, or a rabbit) can be derived from the translation of RNA, or synthesized chemically, and can be conjugated to a carrier protein if desired. Commonly used carrier that are chemically coupled to peptides include bovine serum albumin, thyroglobulin, and keyhole limpet hemocyanin (KLH). The coupled peptide is then used to immunize the animal.


[0041] “Antisense sequence” refers to a sequence capable of specifically hybridizing to a target sequence. The antisense sequence may include DNA, RNA, or any nucleic acid mimic or analog such as peptide nucleic acid (PNA); oligonucleotides having modified backbone linkages such as phosphorothioates, methylphosphonates, or benzylphosphonates; oligonucleotides having modified sugar groups such as 2′-methoxyethyl sugars or 2′-methoxyethoxy sugars; or oligonucleotides having modified bases such as 5-methyl cytosine, 2′-deoxyuracil, or 7-deaza-2′-deoxyguanosine.


[0042] “Antisense sequence” refers to a sequence capable of specifically hybridizing to a target sequence. The antisense sequence can be DNA, RNA, or any nucleic acid mimic or analog.


[0043] “Antisense technology” refers to any technology which relies on the specific hybridization of an antisense sequence to a target sequence.


[0044] A “bin” is a portion of computer memory space used by a computer program for storage of data, and bounded in such a manner that data stored in a bin may be retrieved by the program.


[0045] “Biologically active” refers to an amino acid sequence having a structural, regulatory, or biochemical function of a naturally occurring amino acid sequence.


[0046] “Clone joining” is a process for combining gene bins based upon the bins' containing sequence information from the same clone. The sequences may assemble into a primary gene transcript as well as one or more splice variants.


[0047] “Complementary” describes the relationship between two single-stranded nucleic acid sequences that anneal by base-pairing (5′-A-G-T-3′ pairs with its complement 3′-T-C-A-5′).


[0048] A “component sequence” is a nucleic acid sequence selected by a computer program such as PHRED and used to assemble a consensus or template sequence from one or more component sequences.


[0049] A “consensus sequence” or “template sequence” is a nucleic acid sequence which has been assembled from overlapping sequences, using a computer program for fragment assembly such as the GELVIEW fragment assembly system (Genetics Computer Group (GCG), Madison Wis.) or using a relational database management system (RDMS).


[0050] “Conservative amino acid substitutions” are those substitutions that, when made, least interfere with the properties of the original protein, i.e., the structure and especially the function of the protein is conserved and not significantly changed by such substitutions. The table below shows amino acids which may be substituted for an original amino acid in a protein and which are regarded as conservative substitutions.
1Original ResidueConservative SubstitutionAlaGly, SerArgHis, LysAsnAsp, Gln, HisAspAsn, GluCysAla, SerGlnAsn, Glu, HisGluAsp, Gln, HisGlyAlaHisAsn, Arg, Gln, GluIleLeu, ValLeuIle, ValLysArg, Gln, GluMetLeu, IlePheHis, Met, Leu, Trp, TyrSerCys, ThrThrSer, ValTrpPhe, TyrTyrHis, Phe, TrpValIle, Leu, Thr


[0051] Conservative substitutions generally maintain (a) the structure of the polypeptide backbone in the area of the substitution, for example, as a beta sheet or alpha helical conformation, (b) the charge or hydrophobicity of the molecule at the target site, or (c) the bulk of the side chain.


[0052] “Deletion” refers to a change in either a nucleic or amino acid sequence in which at least one nucleotide or amino acid residue, respectively, is absent.


[0053] “Derivative” refers to the chemical modification of a nucleic acid sequence, such as by replacement of hydrogen by an alkyl, acyl, amino, hydroxyl, or other group.


[0054] “Differential expression” refers to increased or upregulated; or decreased, downregulated, or absent gene or protein expression, determined by comparing at least two different samples. Such comparisons may be carried out between, for example, a treated and an untreated sample, or a diseased and a normal sample.


[0055] The terms “element” and “array element” refer to a polynucleotide, polypeptide, or other chemical compound having a unique and defined position on a microarray.


[0056] “E-value” refers to the statistical probability that a match between two sequences occurred by chance.


[0057] “Exon shuffling” refers to the recombination of different coding regions (exons). Since an exon may represent a structural or functional domain of the encoded protein, new proteins may be assembled through the novel reassortment of stable substructures, thus allowing acceleration of the evolution of new protein functions.


[0058] A “fragment” is a unique portion of mddt or MDDT which is identical in sequence to but shorter in length than the parent sequence. A fragment may comprise up 0 the entire length of the defined sequence, minus one nucleotide/amino acid residue. For example, a fragment may comprise from 10 to 1000 contiguous amino acid residues or nucleotides. A fragment used as a probe, primer, antigen, therapeutic molecule, or for other purposes, may be at least 5, 10, 15, 16, 20, 25, 30, 40, 50, 60, 75, 100, 150, 250 or at least 500 contiguous amino acid residues or nucleotides in length. Fragments may be preferentially selected from certain regions of a molecule. For example, a polypeptide fragment may comprise a certain length of contiguous amino acids selected from the first 250 or 500 amino acids (or first 25% or 50%) of a polypeptide as shown in a certain defined sequence. Clearly these lengths are exemplary, and any length that is supported by the specification, including the Sequence Listing and the figures, may be encompassed by the present embodiments.


[0059] A fragment of mddt comprises a region of unique polynucleotide sequence that specifically identifies mddt, for example, as distinct from any other sequence in the same genome. A fragment of mddt is useful, for example, in hybridization and amplification technologies and in analogous methods that distinguish mddt from related polynucleotide sequences. The precise length of a fragment of mddt and the region of mddt to which the fragment corresponds are routinely determinable by one of ordinary skill in the art based on the intended purpose for the fragment.


[0060] A fragment of MDDT is encoded by a fragment of mddt. A fragment of MDDT comprises a region of unique amino acid sequence that specifically identifies MDDT. For example, a fragment of MDDT is useful as an immunogenic peptide for the development of antibodies that specifically recognize MDDT. The precise length of a fragment of MDDT and the region of MDDT to which the fragment corresponds are routinely determinable by one of ordinary skill in the art based on the intended purpose for the fragment.


[0061] A “full length” nucleotide sequence is one containing at least a start site for translation to a protein sequence, followed by an open reading frame and a stop site, and encoding a “full length” polypeptide.


[0062] “Hit” refers to a sequence whose annotation will be used to describe a given template. Criteria for selecting the top hit are as follows: if the template has one or more exact nucleic acid matches, the top hit is the exact match with highest percent identity. If the template has no exact matches but has significant protein hits, the top hit is the protein hit with the lowest E-value. If the template has no significant protein hits, but does have significant non-exact nucleotide hits, the top hit is the nucleotide hit with the lowest E-value.


[0063] “Homology” refers to sequence similarity either between a reference nucleic acid sequence and at least a fragment of an mddt or between a reference amino acid sequence and a fragment of an MDDT.


[0064] “Hybridization”refers to the process by which a strand of nucleotides anneals with a complementary strand through base pairing. Specific hybridization is an indication that two nucleic acid sequences share a high degree of identity. Specific hybridization complexes form under defined annealing conditions, and remain hybridized after the “washing” step. The defined hybridization conditions include the annealing conditions and the washing step(s), the latter of which is particularly important in determining the stringency of the hybridization process, with more stringent conditions allowing less non-specific binding, i.e., binding between pairs of nucleic acid probes that are not perfectly matched. Permissive conditions for annealing of nucleic acid sequences are routinely determinable and may be consistent among hybridization experiments, whereas wash conditions may be varied among experiments to achieve the desired stringency.


[0065] Generally, stringency of hybridization is expressed with reference to the temperature under which the wash step is carried out. Generally, such wash temperatures are selected to be about 5° C. to 20° C. lower than the thermal melting point (Tm) for the specific sequence at a defined ionic strength and pH. The Tm is the temperature (under defined ionic strength and pH) at which 50% of the target sequence hybridizes to a perfectly matched probe. An equation for calculating Tm and conditions for nucleic acid hybridization is well known and can be found in Sambrook et al., 1989, Molecular Cloning: A Laboratory Manual, 2nd ed., vol. 1-3, Cold Spring Harbor Press, Plainview N.Y.; specifically see volume 2, chapter 9.


[0066] High stringency conditions for hybridization between polynucleotides of the present invention include wash conditions of 68° C. in the presence of about 0.2×SSC and about 0.1% SDS, for 1 hour. Alternatively, temperatures of about 65° C., 60° C., or 55° C. may be used. SSC concentration may be varied from about 0.2 to 2×SSC, with SDS being present at about 0.1%. Typically, blocking reagents are used to block non-specific hybridization. Such blocking reagents include, for instance, denatured salmon sperm DNA at about 100-200 μg/ml. Useful variations on these conditions will be readily apparent to those skilled in the art. Hybridization, particularly under high stringency conditions, may be suggestive of evolutionary similarity between the nucleotides. Such similarity is strongly indicative of a similar role for the nucleotides and their resultant proteins.


[0067] Other parameters, such as temperature, salt concentration, and detergent concentration may be varied to achieve the desired stringency. Denaturants, such as formamide at a concentration of about 35-50% v/v, may also be used under particular circumstances, such as RNA:DNA hybridizations. Appropriate hybridization conditions are routinely determinable by one of ordinary skill in the art.


[0068] “Immunologically active” or “immunogenic” describes the potential for a natural, recombinant, or synthetic peptide, epitope, polypeptide, or protein to induce antibody production in appropriate animals, cells, or cell lines.


[0069] “Insertion” or “assertion” refers to a change in either a nucleic or an amino acid sequence in which at least one nucleon or residue, respectively, is added to the sequence.


[0070] “Labeling” refers to the covalent or noncovalent joining of a polynucleotide, polypeptide, or antibody with a reporter molecule capable of producing a detectable or measurable signal.


[0071] “Microarray” is any arrangement of nucleic acids, amino acids, antibodies, etc., on a substrate. The substrate may be a solid support such as beads, glass, paper, nitrocellulose, nylon, or an appropriate membrane.


[0072] “Linkers” are short stretches of nucleotide sequence which may be added to a vector or an mddt to create restriction endonuclease sites to facilitate cloning. “Polylinkers” are engineered to incorporate multiple restriction enzyme sites and to provide for the use of enzymes which leave 5′ or 3′ overhangs (e.g., BamHI, EcoRI, and HindIII) and those which provide blunt ends (e.g., EcoRV, SnaBI, and StuI).


[0073] “Naturally occurring” refers to an endogenous polynucleotide or polypeptide that may be isolated from viruses or prokaryotic or eukaryotic cells.


[0074] “Nucleic acid sequence” refers to the specific order of nucleotides joined by phosphodiester bonds in a linear, polymeric arrangement. Depending on the number of nucleotides, the nucleic acid sequence can be considered an oligomer, oligonucleotide, or polynucleotide. The nucleic acid can be DNA, RNA, or any nucleic acid analog, such as PNA, may be of genomic or synthetic origin, may be either double-stranded or single-stranded, and can represent either the sense or antisense (complementary) strand.


[0075] “Oligomer” refers to a nucleic acid sequence of at least about 6 nucleotides and as many as about 60 nucleotides, preferably about 15 to 40 nucleotides, and most preferably between about 20 and 30 nucleotides, that may be used in hybridization or amplification technologies. Oligomers may be used as, e.g., primers for PCR, and are usually chemically synthesized.


[0076] “Operably linked” refers to the situation in which a first nucleic acid sequence is placed in a functional relationship with the second nucleic acid sequence. For instance, a promoter is operably linked to a coding sequence if the promoter affects the transcription or expression of the coding sequence. Generally, operably linked DNA sequences may be in close proximity or contiguous and, where necessary to join two protein coding regions, in the same reading frame.


[0077] “Peptide nucleic acid” (PNA) refers to a DNA mimic in which nucleotide bases are attached to a pseudopeptide backbone to increase stability. PNAs, also designated antigene agents, can prevent gene expression by targeting complementary messenger RNA.


[0078] The phrases “percent identity” and “% identity”, as applied to polynucleotide sequences, refer to the percentage of residue matches between at least two polynucleotide sequences aligned using a standardized algorithm. Such an algorithm may insert, in a standardized and reproducible way, gaps in the sequences being compared in order to optimize alignment between two sequences, and therefore achieve a more meaningful comparison of the two sequences.


[0079] Percent identity between polynucleotide sequences may be determined using the default parameters of the CLUSTAL V algorithm as incorporated into the MEGALIGN version 3.12e sequence alignment program. This program is part of the LASERGENE software package, a suite of molecular biological analysis programs (DNASTAR, Madison Wis.). CLUSTAL V is described in Higgins, D. G. and Sharp, P. M. (1989) CABIOS 5:151-153 and in Higgins, D. G. et al. (1992) CABIOS 8:189-191. For pairwise alignments of polynucleotide sequences, the default parameters are set as follows: Ktuple=2, gap penalty=5, window=4, and “diagonals saved”=4. The “weighted” residue weight table is selected as the default. Percent identity is reported by CLUSTAL V as the “percent similarity” between aligned polynucleotide sequence pairs.


[0080] Alternatively, a suite of commonly used and freely available sequence comparison algorithms is provided by the National Center for Biotechnology Information (NCBI) Basic Local Alignment Search Tool (BLAST) (Altschul, S. F. et al. (1990) J. Mol. Biol. 215:403-410), which is available from several sources, including the NCBI, Bethesda, Md., and on the Internet at http://www.ncbi.nlm.nih.gov/BLAST/. The BLAST software suite includes various sequence analysis programs including “blastn,” that is used to determine alignment between a known polynucleotide sequence and other sequences on a variety of databases. Also available is a tool called “BLAST 2 Sequences” that is used for direct pairwise comparison of two nucleotide sequences. “BLAST 2 Sequences” can be accessed and used interactively at http://www.ncbi.nim.nih.gov/gorf/bl2/. The “BLAST 2 Sequences” tool can be used for both blastn and blastp (discussed below). BLAST programs are commonly used with gap and other parameters set to default settings. For example, to compare two nucleotide sequences, one may use blastn with the “BLAST 2 Sequences” tool Version 2.0.9 (May-07-1999) set at default parameters. Such default parameters may be, for example:


[0081] Matrix: BLOSUM62


[0082] Reward for match: 1


[0083] Penalty for mismatch: −2


[0084] Open Gap: 5 and Extension Gap: 2 penalties


[0085] Gap x drop-off: 50


[0086] Expect: 10


[0087] Word Size: 11


[0088] Filter: on


[0089] Percent identity may be measured over the length of an entire defined sequence, for example, as defined by a particular SEQ ID number, or may be measured over a shorter length, for example, over the length of a fragment taken from a larger, defined sequence, for instance, a fragment of at least 20, at least 30, at least 40, at least 50, at least 70, at least 100, or at least 200 contiguous nucleotides. Such lengths are exemplary only, and it is understood that any fragment length supported by the sequences shown herein, in figures or Sequence Listings, may be used to describe a length over which percentage identity may be measured.


[0090] Nucleic acid sequences that do not show a high degree of identity may nevertheless encode similar amino acid sequences due to the degeneracy of the genetic code. It is understood that changes in nucleic acid sequence can be made using this degeneracy to produce multiple nucleic acid sequences that all encode substantially the same protein.


[0091] The phrases “percent identity” and “% identity”, as applied to polypeptide sequences, refer to the percentage of residue matches between at least two polypeptide sequences aligned using a standardized algorithm. Methods of polypeptide sequence alignment are well-known. Some alignment methods take into account conservative amino acid substitutions. Such conservative substitutions, explained in more detail above, generally preserve the hydrophobicity and acidity of the substituted residue, thus preserving the structure (and therefore function) of the folded polypeptide.


[0092] Percent identity between polypeptide sequences may be determined using the default parameters of the CLUSTAL V algorithm as incorporated into the MEGALIGN version 3.12e sequence alignment program (described and referenced above). For pairwise alignments of polypeptide sequences using CLUSTAL V, the default parameters are set as follows: Ktuple=1, gap penalty=3, window=5, and “diagonals saved”=5. The PAM250 matrix is selected as the default residue weight table. As with polynucleotide alignments, the percent identity is reported by CLUSTAL V as the “percent similarity” between aligned polypeptide sequence pairs.


[0093] Alternatively the NCBI BLAST software suite may be used. For example, for a pairwise comparison of two polypeptide sequences, one may use the “BLAST 2 Sequences” tool Version 2.0.9 (May-07-1999) with blastp set at default parameters. Such default parameters may be, for example:


[0094] Matrix: BLOSUM62


[0095] Open Gap: 11 and Extension Gap: 1 penalty


[0096] Gap x drop-off: 50


[0097] Expect: 10


[0098] Word Size: 3


[0099] Filter: on


[0100] Percent identity may be measured over the length of an entire defined polypeptide sequence, for example, as defined by a particular SEQ ID number, or may be measured over a shorter length, for example, over the length of a fragment taken from a larger, defined polypeptide sequence, for instance, a fragment of at least 15, at least 20, at least 30, at least 40, at least 50, at least 70 or at least 150 contiguous residues. Such lengths are exemplary only, and it is understood that any fragment length supported by the sequences shown herein, in figures or Sequence listings, may be used to describe a length over which percentage identity may be measured.


[0101] “Post-translational modification” of an MDDT may involve lipidation, glycosylation, phosphorylation, acetylation, racemization, proteolytic cleavage, and other modifications known in the art. These processes may occur synthetically or biochemically. Biochemical modifications will vary by cell type depending on the enzymatic milieu and the MDDT.


[0102] “Probe” refers to mddt or fragments thereof, which are used to detect identical, allelic or related nucleic acid sequences. Probes are isolated oligonucleotides or polynucleotides attached to a detectable label or reporter molecule. Typical labels include radioactive isotopes, ligands, chemiluminescent agents, and enzymes. “Primers” are short nucleic acids, usually DNA oligonucleotides, which may be annealed to a target polynucleotide by complementary base-pairing. The primer may then be extended along the target DNA strand by a DNA polymerase enzyme. Primer pairs can be used for amplification (and identification) of a nucleic acid sequence, e.g., by the polymerase chain reaction (PCR).


[0103] Probes and primers as used in the present invention typically comprise at least 15 contiguous nucleotides of a known sequence. In order to enhance specificity, longer probes and primers may also be employed, such as probes and primers that comprise at least 20, 30, 40, 50, 60, 70, 80, 90, 100, or at least 150 consecutive nucleotides of the disclosed nucleic acid sequences. Probes and primers may be considerably longer than these examples, and it is understood that any length supported by the specification, including the figures and Sequence Listing, may be used.


[0104] Methods for preparing and using probes and primers are described in the references, for example Sambrook et al., 1989, Molecular Cloning: A Laboratory Manual, 2nd ed., vol. 1-3, Cold Spring Harbor Press, Plainview N.Y.; Ausubel et al.,1987, Current Protocols in Molecular Biology, Greene Publ. Assoc. & Wiley-Intersciences, New York N.Y.; Innis et al., 1990, PCR Protocols, A Guide to Methods and Applications, Academic Press, San Diego Calif. PCR primer pairs can be derived from a known sequence, for example, by using computer programs intended for that purpose such as Primer (Version 0.5, 1991, Whitehead Institute for Biomedical Research, Cambridge Mass.).


[0105] Oligonucleotides for use as primers are selected using software known in the art for such purpose. For example, OLIGO 4.06 software is useful for the selection of PCR primer pairs of up to 100 nucleotides each, and for the analysis of oligonucleotides and larger polynucleotides of up to 5,000 nucleotides from an input polynucleotide sequence of up to 32 kilobases. Similar primer selection programs have incorporated additional features for expanded capabilities. For example, the PrimOU primer selection program (available to the public from the Genome Center at University of Texas South West Medical Center, Dallas Tex.) is capable of choosing specific primers from megabase sequences and is thus useful for designing primers on a genome-wide scope. The Primer3 primer selection program (available to the public from the Whitehead Institute/ Center for Genome Research, Cambridge Mass.) allows the user to input a “mispriming library.” in which sequences to avoid as primer binding sites are user-specified. Primer3 is useful, in particular, for the selection of oligonucleotides for microarrays. (The source code for the latter two primer selection programs may also be obtained from their respective sources and modified to meet the user's specific needs.) The PrimeGen program (available to the public from the UK Human Genome Mapping Project Resource Centre, Cambridge UK) designs primers based on multiple sequence alignments, thereby allowing selection of primers that hybridize to either the most conserved or least conserved regions of aligned nucleic acid sequences. Hence, this program is useful for identification of both unique and conserved oligonucleotides and polynucleotide fragments. The oligonucleotides and polynucleotide fragments identified by any of the above selection methods are useful in hybridization technologies, for example, as PCR or sequencing primers, microarray elements, or specific probes to identify fully or partially complementary polynucleotides in a sample of nucleic acids. Methods of oligonucleotide selection are not limited to those described above.


[0106] “Purified” refers to molecules, either polynucleotides or polypeptides that are isolated or separated from their natural environment and are at least 60% free, preferably at least 75% free, and most preferably at least 90% free from other compounds with which they are naturally associated.


[0107] A “recombinant nucleic acid” is a sequence that is not naturally occurring or has a sequence that is made by an artificial combination of two or more otherwise separated segments of sequence. This artificial combination is often accomplished by chemical synthesis or, more commonly, by the artificial manipulation of isolated segments of nucleic acids, e.g., by genetic engineering techniques such as those described in Sambrook, supra. The term recombinant includes nucleic acids that have been altered solely by addition, substitution, or deletion of a portion of the nucleic acid. Frequently, a recombinant nucleic acid may include a nucleic acid sequence operably linked to a promoter sequence. Such a recombinant nucleic acid may be part of a vector that is used, for example, to transform a cell.


[0108] Alternatively, such recombinant nucleic acids may be part of a viral vector, e.g., based on a vaccinia virus, that could be use to vaccinate a mammal wherein the recombinant nucleic acid is expressed, inducing a protective immunological response in the mammal.


[0109] “Regulatory element” refers to a nucleic acid sequence from nontranslated regions of a gene, and includes enhancers, promoters, introns, and 3′ untranslated regions, which interact with host proteins to carry out or regulate transcription or translation.


[0110] “Reporter” molecules are chemical or biochemical moieties used for labeling a nucleic acid, an amino acid, or an antibody. They include radionuclides; enzymes; fluorescent, chemiluminescent, or chromogenic agents; substrates; cofactors; inhibitors; magnetic particles; and other moieties known in the art.


[0111] An “RNA equivalent” in reference to a DNA sequence, is composed of the same linear sequence of nucleotides as the reference DNA sequence with the exception that all occurrences of the nitrogenous base thymine are replaced with uracil, and the sugar backbone is composed of ribose instead of deoxyribose.


[0112] “Sample” is used in its broadest sense. Samples may contain nucleic or amino acids, antibodies, or other materials, and may be derived from any source (e.g., bodily fluids including, but not limited to, saliva, blood, and urine; chromosome(s), organelles, or membranes isolated from a cell; genomic DNA, RNA, or cDNA in solution or bound to a substrate; and cleared cells or tissues or blots or imprints from such cells or tissues).


[0113] “Specific binding” or “specifically binding” refers to the interaction between a protein or peptide and its agonist, antibody, antagonist, or other binding partner. The interaction is dependent upon the presence of a particular structure of the protein, e.g., the antigenic determinant or epitope, recognized by the binding molecule. For example, if an antibody is specific for epitope “A,” the presence of a polypeptide containing epitope A, or the presence of free unlabeled A, in a reaction containing free labeled A and the antibody will reduce the amount of labeled A that binds to the antibody.


[0114] “Substitution” refers to the replacement of at least one nucleotide or amino acid by a different nucleotide or amino acid.


[0115] “Substrate” refers to any suitable rigid or semi-rigid support including, e.g., membranes, filters, chips, slides, wafers, fibers, magnetic or nonmagnetic beads, gels, tubing, plates, polymers, microparticles or capillaries. The substrate can have a variety of surface forms, such as wells, trenches, pins, channels and pores, to which polynucleotides or polypeptides are bound.


[0116] A “transcript image” refers to the collective pattern of gene expression by a particular tissue or cell type under given conditions at a given time.


[0117] “Transformation” refers to a process by which exogenous DNA enters a recipient cell. Transformation may occur under natural or artificial conditions using various methods well known in the art. Transformation may rely on any known method for the insertion of foreign nucleic acid sequences into a prokaryotic or eukaryotic host cell. The method is selected based on the host cell being transformed.


[0118] “Transformants” include stably transformed cells in which the inserted DNA is capable of replication either as an autonomously replicating plasmid or as part of the host chromosome, as well as cells which transiently express inserted DNA or RNA.


[0119] A “transgenic organism,” as used herein, is any organism, including but not limited to animals and plants, in which one or more of the cells of the organism contains heterologous nucleic acid introduced by way of human intervention, such as by transgenic techniques well known in the art. The nucleic acid is introduced into the cell, directly or indirectly by introduced into a precursor of the cell, by way of deliberate genetic manipulation, such as by microinjection or by infection with a recombinant virus. The term genetic manipulation does not include classical cross-breeding, or in vitro fertilization, but rather is directed to the introduction of a recombinant DNA molecule. The transgenic organisms contemplated in accordance with the present invention include bacteria, cyanobacteria, fungi, and plants and animals. The isolated DNA of the present invention can be introduced into the host by methods known in the art, for example infection, transfection, transformation or transconjugation. Techniques for transferring the DNA of the present invention into such organisms are widely known and provided in references such as Sambrook et al. (1989), supra.


[0120] A “variant” of a particular nucleic acid sequence is defined as a nucleic acid sequence having at least 25% sequence identity to the particular nucleic acid sequence over a certain length of one of the nucleic acid sequences using blastn with the “BLAST 2 Sequences” tool Version 2.0.9 (May-07-1999) set at default parameters. Such a pair of nucleic acids may show, for example, at least 30%, at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% or greater sequence identity over a certain defined length. The variant may result in “conservative” amino acid changes which do not affect structural and/or chemical properties. A variant may be described as, for example, an “allelic” (as defined above), “splice,” “species,” or “polymorphic” variant. A splice variant may have significant identity to a reference molecule, but will generally have a greater or lesser number of polynucleotides due to alternate splicing of exons during mRNA processing. The corresponding polypeptide may possess additional functional domains or lack domains that are present in the reference molecule. Species variants are polynucleotide sequences that vary from one species to another. The resulting polypeptides generally will have significant amino acid identity relative to each other. A polymorphic variant is a variation in the polynucleotide sequence of a particular gene between individuals of a given species. Polymorphic variants also may encompass “single nucleotide polymorphisms” (SNPs) in which the polynucleotide sequence varies by one base. The presence of SNPs may be indicative of, for example, a certain population, a disease state, or a propensity for a disease state.


[0121] In an alternative, variants of the polynucleotides of the present invention may be generated through recombinant methods. One possible method is a DNA shuffling technique such as MOLECULARBREEDING (Maxygen Inc., Santa Clara Calif.; described in U.S. Pat. No. 5,837,458; Chang, C. -C. et al. (1999) Nat. Biotechnol. 17:793-797; Christians, F. C. et al. (1999) Nat. Biotechnol. 17:259-264; and Crameri, A. et al. (1996) Nat. Biotechnol. 14:315-319) to alter or improve the biological properties of MDDT, such as its biological or enzymatic activity or its ability to bind to other molecules or compounds. DNA shuffling is a process by which a library of gene variants is produced using PCR-method recombination of gene fragments. The library is then subjected to selection or screening procedures that identify those gene variants with the desired properties. These preferred variants may then be pooled and further subjected to recursive rounds of DNA shuffling and selection/screening. Thus, genetic diversity is created through “artificial” breeding and rapid molecular evolution. For example, fragments of a single gene containing random point mutations may be recombined, screened, and then reshuffled until the desired properties are optimized. Alternatively, fragments of a given gene may be recombined with fragments of homologous genes in the same gene family, either from the same or different species, thereby maximizing the genetic diversity of multiple naturally occurring genes in a directed and controllable manner.


[0122] A “variant” of a particular polypeptide sequence is defined as a polypeptide sequence having at least 40% sequence identity to the particular polypeptide sequence over a certain length of one of the polypeptide sequences using blastp with the “BLAST 2 Sequences” tool Version 2.0.9 (May-07-1999) set at default parameters. Such a pair of polypeptides may show, for example, at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% or greater sequence identity over a certain defined length of one of the polypeptides.



THE INVENTION

[0123] In a particular embodiment, cDNA sequences derived from human tissues and cell lines were aligned based on nucleotide sequence identity and assembled into “consensus” or “template” sequences which are designated by the template identification numbers (template IDs) in column 2 of Table 2. The sequence identification numbers (SEQ ID NO:s) corresponding to the template IDs are shown in column 1. The template sequences have similarity to GenBank sequences, or “hits,” as designated by the GI Numbers in column 3. The statistical probability of each GenBank hit is indicated by a probability score in column 4, and the functional annotation corresponding to each GenBank hit is listed in column 5.


[0124] The invention incorporates the nucleic acid sequences of these templates as disclosed in the Sequence Listing and the use of these sequences in the diagnosis and treatment of disease states characterized by defects in disease detection and treatment molecules. The invention further utilizes these sequences in hybridization and amplification technologies, and in particular, in technologies which assess gene expression patterns correlated with specific cells or tissues and their responses in vivo or in vitro to pharmaceutical agents, toxins, and other treatments. In this manner, the sequences of the present invention are used to develop a transcript image for a particular cell or tissue.


[0125] Derivation of Nucleic Acid Sequences


[0126] cDNA was isolated from libraries constructed using RNA derived from normal and diseased human tissues and cell lines. The human tissues and cell lines used for cDNA library construction were selected from a broad range of sources to provide a diverse population of cDNAs representative of gene transcription throughout the human body. Descriptions of the human tissues and cell lines used for cDNA library construction are provided in the LIFESEQ database (Incyte Genomics, Inc. (Incyte), Palo Alto Calif.). Human tissues were broadly selected from, for example, cardiovascular, dermatologic, endocrine, gastrointestinal, hematopoietic/immune system, musculoskeletal, neural, reproductive, and urologic sources.


[0127] Cell lines used for cDNA library construction were derived from, for example, leukemic cells, teratocarcinomas, neuroepitheliomas, cervical carcinoma, lung fibroblasts, and endothelial cells. Such cell lines include, for example, THP-1, Jurkat, HUVEC, hNT2, WI38, HeLa, and other cell lines commonly used and available from public depositories (American Type Culture Collection, Manassas Va.). Prior to mRNA isolation, cell lines were untreated, treated with a pharmaceutical agent such as 5′-aza-2′-deoxycytidine, treated with an activating agent such as lipopolysaccharide in the case of leukocytic cell lines, or, in the case of endothelial cell lines, subjected to shear stress.


[0128] Sequencing of the cDNAs


[0129] Methods for DNA sequencing are well known in the art. Conventional enzymatic methods employ the Klenow fragment of DNA polymerase I, SEQUENASE DNA polymerase (U.S. Biochemical Corporation, Cleveland Ohio), Taq polymerase (Applied Biosystems, Foster City Calif.), thermostable T7 polymerase (Amersham Pharmacia Biotech, Inc. (Amersham Pharmacia Biotech), Piscataway N.J.), or combinations of polymerases and proofreading exonucleases such as those found in the ELONGASE amplification system (Life Technologies Inc. (Life Technologies), Gaithersburg Md.), to extend the nucleic acid sequence from an oligonucleotide primer annealed to the DNA template of interest. Methods have been developed for the use of both single-stranded and double-stranded templates. Chain termination reaction products may be electrophoresed on urea-polyacrylamide gels and detected either by autoradiography (for radioisotope-labeled nucleotides) or by fluorescence (for fluorophore-labeled nucleotides). Automated methods for mechanized reaction preparation, sequencing, and analysis using fluorescence detection methods have been developed. Machines used to prepare cDNAs for sequencing can include the MICROLAB 2200 liquid transfer system (Hamilton Company (Hamilton), Reno Nev.), Peltier thermal cycler (PTC200; MJ Research, Inc. (MJ Research), Watertown Mass.), and ABI CATALYST 800 thermal cycler (Applied Biosystems). Sequencing can be carried out using, for example, the ABI 373 or 377 (Applied Biosystems) or MEGABACE 1000 (Molecular Dynamics, Inc. (Molecular Dynamics), Sunnyvale Calif.) DNA sequencing systems, or other automated and manual sequencing systems well known in the art.


[0130] The nucleotide sequences of the Sequence Listing have been prepared by current, state-of-the-art, automated methods and, as such, may contain occasional sequencing errors or unidentified nucleotides. Such unidentified nucleotides are designated by an N. These infrequent unidentified bases do not represent a hindrance to practicing the invention for those skilled in the art. Several methods employing standard recombinant techniques may be used to correct errors and complete the missing sequence information. (See, e.g., those described in Ausubel, F. M. et al. (1997) Short Protocols in Molecular Biology, John Wiley & Sons, New York N.Y.; and Sambrook, J. et al. (1989) Molecular Cloning, A Laboratory Manual, Cold Spring Harbor Press, Plainview N.Y.)


[0131] Assembly of cDNA Sequences


[0132] Human polynucleotide sequences may be assembled using programs or algorithms well known in the art. Sequences to be assembled are related, wholly or in part, and may be derived from a single or many different transcripts. Assembly of the sequences can be performed using such programs as PHRAP (Phils Revised Assembly Program) and the GELVIEW fragment assembly system (GCG), or other methods known in the art.


[0133] Alternatively, cDNA sequences are used as “component” sequences that are assembled into “template” or “consensus” sequences as follows. Sequence chromatograms are processed, verified, and quality scores are obtained using PHRED. Raw sequences are edited using an editing pathway known as Block 1 (See, e.g., the LIFESEQ Assembled User Guide, Incyte Genomics, Palo Alto, Calif.). A series of BLAST comparisons is performed and low-information segments and repetitive elements (e.g., dinucleotide repeats, Alu repeats, etc.) are replaced by “n's”, or masked, to prevent spurious matches. Mitochondrial and ribosomal RNA sequences are also removed. The processed sequences are then loaded into a relational database management system (RDMS) which assigns edited sequences to existing templates, if available. When additional sequences are added into the RDMS, a process is initiated which modifies existing templates or creates new templates from works in progress (i.e., nonfinal assembled sequences) containing queued sequences or the sequences themselves. After the new sequences have been assigned to templates, the templates can be merged into bins. If multiple templates exist in one bin, the bin can be split and the templates reannotated.


[0134] Once gene bins have been generated based upon sequence alignments, bins are “clone joined” based upon clone information. Clone joining occurs when the 5′ sequence of one clone is present in one bin and the 3′ sequence from the same clone is present in a different bin, indicating that the two bins should be merged into a single bin. Only bins which share at least two different clones are merged.


[0135] A resultant template sequence may contain either a partial or a full length open reading frame, or all or part of a genetic regulatory element. This variation is due in part to the fact that the full length cDNAs of many genes are several hundred, and sometimes several thousand, bases in length. With current technology, cDNAs comprising the coding regions of large genes cannot be cloned because of vector limitations, incomplete reverse transcription of the mRNA, or incomplete “second strand” synthesis. Template sequences may be extended to include additional contiguous sequences derived from the parent RNA transcript using a variety of methods known to those of skill in the art. Extension may thus be used to achieve the full length coding sequence of a gene.


[0136] Analysis of the cDNA Sequences


[0137] The cDNA sequences are analyzed using a variety of programs and algorithms which are well known in the art. (See, e.g., Ausubel, 1997, supra, Chapter 7.7; Meyers, R. A. (Ed.) (1995) Molecular Biology and Biotechnology, Wiley VCH, New York N.Y., pp. 856-853; and Table 8.) These analyses comprise both reading frame determinations, e.g., based on triplet codon periodicity for particular organisms (Fickett, J. W. (1982) Nucleic Acids Res. 10:5303-5318); analyses of potential start and stop codons; and homology searches.


[0138] Computer programs known to those of skill in the art for performing computer-assisted searches for amino acid and nucleic acid sequence similarity, include, for example, Basic Local Alignment Search Tool (BLAST; Altschul, S. F. (1993) J. Mol. Evol. 36:290-300; Altschul, S. F. et al. (1990) J. Mol. Biol. 215:403-410). BLAST is especially useful in determining exact matches and comparing two sequence fragments of arbitrary but equal lengths, whose alignment is locally maximal and for which the alignment score meets or exceeds a threshold or cutoff score set by the user (Karlin, S. et al. (1988) Proc. Natl. Acad. Sci. USA 85:841-845). Using an appropriate search tool (e.g., BLAST or HMM), GenBank, SwissProt, BLOCKS, PFAM and other databases may be searched for sequences containing regions of homology to a query mddt or MDDT of the present invention.


[0139] Other approaches to the identification, assembly, storage, and display of nucleotide and polypeptide sequences are provided in “Relational Database for Storing Biomolecule Information,” U.S. Ser. No. 08/947,845, filed Oct. 9, 1997; “Project-Based Full-Length Biomolecular Sequence Database,” U.S. Ser. No. 08/811,758, filed Mar. 6, 1997; and “Relational Database and System for Storing Information Relating to Biomolecular Sequences,” U.S. Ser. No. 09/034,807, filed Mar. 4, 1998, all of which are incorporated by reference herein in their entirety.


[0140] Protein hierarchies can be assigned to the putative encoded polypeptide based on, e.g., motif, BLAST, or biological analysis. Methods for assigning these hierarchies are described, for example, in “Database System Employing Protein Function Hierarchies for Viewing Biomolecular Sequence Data,” U.S. Ser. No. 08/812,290, filed Mar. 6, 1997, incorporated herein by reference.


[0141] Human Disease Detection and Treatment Molecule Sequences


[0142] The mddt of the present invention may be used for a variety of diagnostic and therapeutic purposes. For example, an mddt may be used to diagnose a particular condition, disease, or disorder associated with disease detection and treatment molecules. Such conditions, diseases, and disorders include, but are not limited to, a cell proliferative disorder, such as actinic keratosis, arteriosclerosis, atherosclerosis, bursitis, cirrhosis, hepatitis, mixed connective tissue disease (MCTD), myelofibrosis, paroxysmal nocturnal hemoglobinuria, polycythemia vera, psoriasis, primary thrombocythemia, and cancers including adenocarcinoma, leukemia, lymphoma, melanoma, myeloma, sarcoma, teratocarcinoma, and, in particular, a cancer of the adrenal gland, bladder, bone, bone marrow, brain, breast, cervix, gall bladder, ganglia, gastrointestinal tract, heart, kidney, liver, lung, muscle, ovary, pancreas, parathyroid, penis, prostate, salivary glands, skin, spleen, testis, thymus, thyroid, and uterus; and an autoimmune/inflammatory disorder, such as actinic keratosis, acquired immunodeficiency syndrome (AIDS), Addison's disease, adult respiratory distress syndrome, allergies, ankylosing spondylitis, amyloidosis, anemia, arteriosclerosis, asthma, atherosclerosis, autoimmune hemolytic anemia, autoimmune thyroiditis, bronchitis, bursitis, cholecystitis, cirrhosis, contact dermatitis, Crohn's disease, atopic dermatitis, dermatomyositis, diabetes mellitus, emphysema, erythroblastosis fetalis, erythema nodosum, atrophic gastritis, glomerulonephritis, Goodpasture's syndrome, gout, Graves' disease, Hashimoto's thyroiditis, paroxysmal nocturnal hemoglobinuria, hepatitis, hypereosinophilia, irritable bowel syndrome, episodic lymphopenia with lymphocytotoxins, mixed connective tissue disease (MCTD), multiple sclerosis, myasthenia gravis, myocardial or pericardial inflammation, myelofibrosis, osteoarthritis, osteoporosis, pancreatitis, polycythemia vera, polymyositis, psoriasis, Reiter's syndrome, rheumatoid arthritis, scleroderma, Sjögren's syndrome, systemic anaphylaxis, systemic lupus erythematosus, systemic sclerosis, primary thrombocythemia, thrombocytopenic purpura, ulcerative colitis, uveitis. Werner syndrome, complications of cancer, hemodialysis, and extracorporeal circulation, trauma, and hematopoietic cancer including lymphoma, leukemia, and myeloma. The mddt can be used to detect the presence of, or to quantify the amount of, an mddt-related polynucleotide in a sample. This information is then compared to information obtained from appropriate reference samples, and a diagnosis is established. Alternatively, a polynucleotide complementary to a given mddt can inhibit or inactivate a therapeutically relevant gene related to the mddt.


[0143] Analysis of mddt Expression Patterns


[0144] The expression of mddt may be routinely assessed by hybridization-based methods to determine, for example, the tissue-specificity, disease-specificity, or developmental stage-specificity of mddt expression. For example, the level of expression of mddt may be prepared among different cell types or tissues, among diseased and normal cell types or tissues, among cell types or tissues at different developmental stages, or among cell types or tissues undergoing various treatments. This type of analysis is useful, for example, to assess the relative levels of mddt expression in fully or partially differentiated cells or tissues, to determine if changes in mddt expression levels are correlated with the development or progression of specific disease states, and to assess the response of a cell or tissue to a specific therapy, for example, in pharmacological or toxicological studies. Methods for the analysis of mddt expression are based on hybridization and amplification technologies and include membrane-based procedures such as northern blot analysis, high-throughput procedures that utilize, for example, microarrays, and PCR-based procedures.


[0145] Hybridization and Genetic Analysis


[0146] The mddt, their fragments, or complementary sequences, may be used to identify the presence of and/or to determine the degree of similarity between two (or more) nucleic acid sequences. The mddt may be hybridized to naturally occurring or recombinant nucleic acid sequences under appropriately selected temperatures and salt concentrations. Hybridization with a probe based on the nucleic acid sequence of at least one of the mddt allows for the detection of nucleic acid sequences, including genomic sequences, which are identical or related to the mddt of the Sequence Listing. Probes may be selected from non-conserved or unique regions of at least one of the polynucleotides of SEQ ID NO:1-252 and tested for their ability to identify or amplify the target nucleic acid sequence using standard protocols.


[0147] Polynucleotide sequences that are capable of hybridizing, in particular, to those shown in SEQ ID NO:1-252 and fragments thereof, can be identified using various conditions of stringency. (See, e.g., Wahl, G. M. and S. L. Berger (1987) Methods Enzymol. 152:399-407; Kimmel, A. R. (1987) Methods Enzymol. 152:507-511.) Hybridization conditions are discussed in “Definitions.”


[0148] A probe for use in Southern or northern hybridization may be derived from a fragment of an mddt sequence, or its complement, that is up to several hundred nucleotides in length and is either single-stranded or double-stranded. Such probes may be hybridized in solution to biological materials such as plasmids, bacterial, yeast, or human artificial chromosomes, cleared or sectioned tissues, or to artificial substrates containing mddt. Microarrays are particularly suitable for identifying the presence of and detecting the level of expression for multiple genes of interest by examining gene expression correlated with, e.g., various stages of development, treatment with a drug or compound, or disease progression. An array analogous to a dot or slot blot may be used to arrange and link polynucleotides to the surface of a substrate using one or more of the following: mechanical (vacuum), chemical, thermal, or UV bonding procedures. Such an array may contain any number of mddt and may be produced by hand or by available devices, materials, and machines.


[0149] Microarrays may prepared, used, and analyzed using methods own in the art. (See, e.g., Brennan, T. M. et al. (1995) U.S. Pat. No. 5,474,796; Schena, M. et al. (1996) Proc. Natl. Acad. Sci. USA 93:10614-10619; Baldeschweiler et al. (1995) PCT application WO95/251116; Shalon, D. et al. (1995) PCT application WO95/35505; Heller, R. A. et al. (1997) Proc. Natl. Acad. Sci. USA 94:2150-2155; and Heller, M. J. et al. (1997) U.S. Pat. No. 5,605,662.)


[0150] Probes may be labeled by either PCR or enzymatic techniques using a variety of commercially available reporter molecules. For example, commercial kits are available for radioactive and chemiluminescent labeling (Amersham Pharmacia Biotech) and for alkaline phosphatase labeling (Life Technologies). Alternatively, mddt may be cloned into commercially available vectors for the production of RNA probes. Such probes may be transcribed in the presence of at least one labeled nucleotide (e.g., 32P-ATP, Amersham Pharmacia Biotech).


[0151] Additionally the polynucleotides of SEQ ID NO:1-252 or suitable fragments thereof can be used to isolate full length cDNA sequences utilizing hybridization and/or amplification procedures well known in the art, e.g., cDNA library screening, PCR amplification, etc. The molecular cloning of such full length cDNA sequences may employ the method of cDNA library screening with probes using the hybridization, stringency, washing, and probing strategies described above and in Ausubel, supra, Chapters 3, 5, and 6. These procedures may also be employed with genomic libraries to isolate genomic sequences of mddt in order to analyze, e.g., regulatory elements.


[0152] Genetic Mapping


[0153] Gene identification and mapping are important in the investigation and treatment of almost all conditions, diseases, and disorders. Cancer, cardiovascular disease, Alzheimer's disease, arthritis, diabetes, and mental illnesses are of particular interest. Each of these conditions is more complex than the single gene defects of sickle cell anemia or cystic fibrosis, with select groups of genes being predictive of predisposition for a particular condition, disease, or disorder. For example, cardiovascular disease may result from malfunctioning receptor molecules that fail to clear cholesterol from the bloodstream, and diabetes may result when a particular individual's immune system is activated by an infection and attacks the insulin-producing cells of the pancreas. In some studies, Alzheimer's disease has been linked to a gene on chromosome 21; other studies predict a different gene and location. Mapping of disease genes is a complex and reiterative process and generally proceeds from genetic linkage analysis to physical mapping.


[0154] As a condition is noted among members of a family, a genetic linkage map traces parts of chromosomes that are inherited in the same pattern as the condition. Statistics link the inheritance of particular conditions to particular regions of chromosomes, as defined by RFLP or other markers. (See, for example, Lande S. and Botstein, D. (1986) Proc. Natl. Acad. Sci. USA 83:7353-7357.) Occasionally, genetic markers and their locations are known from previous studies. More often, however, the markers are simply stretches of DNA that differ among individuals. Examples of genetic linkage maps can be found in various scientific journals or at the Online Mendelian Inheritance in Man (OMIM) World Wide Web site.


[0155] In another embodiment of the invention, mddt sequences may be used to generate hybridization probes useful in chromosomal mapping of naturally occurring genomic sequences. Either coding or noncoding sequences of mddt may be used, and in some instances, noncoding sequences may be preferable over coding sequences. For example, conservation of an mddt coding sequence among members of a multi-gene family may potentially cause undesired cross hybridization during chromosomal mapping. The sequences may be mapped to a particular chromosome, to a specific region of a chromosome, or to artificial chromosome constructions, e.g., human artificial chromosomes (HACs), yeast artificial chromosomes (YACs), bacterial artificial chromosomes (BACs), bacterial P1 constructions, or single chromosome cDNA libraries. (See, e.g., Harrington, J. J. et al. (1997) Nat. Genet. 15:345-355; Price, C. M. (1993) Blood Rev. 7:127-134; and Trask, B. J. (1991) Trends Genet. 7:149-154.)


[0156] Fluorescent in situ hybridization (FISH) may be correlated with other physical chromosome mapping techniques and genetic map data. (See, e.g., Meyers, supra, pp. 965-968.) Correlation between the location of mddt on a physical chromosomal map and a specific disorder, or a predisposition to a specific disorder, may help define the region of DNA associated with that disorder. The mddt sequences may also be used to detect polymorphisms that are genetically linked to the inheritance of a particular condition, disease, or disorder.


[0157] In situ hybridization of chromosomal preparations and genetic mapping techniques, such as linkage analysis using established chromosomal markers, may be used for extending existing genetic maps. Often the placement of a gene on the chromosome of another mammalian species, such as mouse, may reveal associated markers even if the number or arm of the corresponding human chromosome is not known. These new marker sequences can be mapped to human chromosomes and may provide valuable information to investigators searching for disease genes using positional cloning or other gene discovery techniques. Once a disease or syndrome has been crudely correlated by genetic linkage with a particular genomic region, e.g., ataxia-telangiectasia to 11q22-23, any sequences mapping to that area may represent associated or regulatory genes for further investigation. (See, e.g., Gatti, R. A. et al. (1988) Nature 336:577-580.) The nucleotide sequences of the subject invention may also be used to detect differences in chromosomal architecture due to translocation, inversion, etc., among normal, carrier, or affected individuals.


[0158] Once a disease-associated gene is mapped to a chromosomal region, the gene must be cloned in order to identify mutant or other alterations (e.g., translocations oesions) that may be correlated with disease. This process requires a physical map of the chromosomal region containing the disease-gene of interest along with associated markers. A physical map is necessary for determining the nucleotide sequence of and order of marker genes on a particular chromosomal region. Physical mapping techniques are well known in the art and require the generation of overlapping sets of cloned DNA fragments from a particular organelle, chromosome, or genome. These clones are analyzed to reconstruct and catalog their order. Once the position of a marker is determined, the DNA from that region is obtained by consulting the catalog and selecting clones from that region. The gene of interest is located through positional cloning techniques using hybridization or similar methods.


[0159] Diagnostic Uses


[0160] The mddt of the present invention may be used to design probes useful in diagnostic assays. Such assays, well known to those skilled in the art, may be used to detect or confirm conditions, disorders, or diseases associated with abnormal levels of mddt expression. Labeled probes developed from mddt sequences are added to a sample under hybridizing conditions of desired stringency. In some instances, mddt, or fragments or oligonucleotides derived from mddt, may be used as primers in amplification steps prior to hybridization. The amount of hybridization complex formed is quantified and compared with standards for that cell or tissue. If mddt expression varies significantly from the standard, the assay indicates the presence of the condition, disorder, or disease. Qualitative or quantitative diagnostic methods may include northern, dot blot, or other membrane or dip-stick based technologies or multiple-sample format technologies such as PCR, enzyme-linked immunosorbent assay (ELISA)-like, pin, or chip-based assays.


[0161] The probes described above may also be used to monitor the progress of conditions, disorders, or diseases associated with abnormal levels of mddt expression, or to evaluate the efficacy of a particular therapeutic treatment. The candidate probe may be identified from the mddt that are specific to a given human tissue and have not been observed in GenBank or other genome databases. Such a probe may be used in animal studies, preclinical tests, clinical trials, or in monitoring the treatment of an individual patient. In a typical process, standard expression is established by methods well known in the art for use as a basis of comparison, samples from patients affected by the disorder or disease are combined with the probe to evaluate any deviation from the standard profile, and a therapeutic agent is administered and effects are monitored to generate a treatment profile. Efficacy is evaluated by determining whether the expression progresses toward or returns to the standard normal pattern. Treatment profiles may be generated over a period of several days or several months. Statistical methods well known to those skilled in the art may be use to determine the significance of such therapeutic agents.


[0162] The polynucleotides are also useful for identifying individuals from minute biological samples, for example, by matching the RFLP pattern of a sample's DNA to that of an individual's DNA. The polynucleotides of the present invention can also be used to determine the actual base-by-base DNA sequence of selected portions of an individual's genome. These sequences can be used to prepare PCR primers for amplifying and isolating such selected DNA, which can then be sequenced. Using this technique, an individual can be identified through a unique set of DNA sequences. Once a unique ID database is established for an individual, positive identification of that individual can be made from extremely small tissue samples.


[0163] In a particular aspect, oligonucleotide primers derived from the mddt of the invention may be used to detect single nucleotide polymorphisms (SNPs). SNPs are substitutions, insertions and deletions that are a frequent cause of inherited or acquired genetic disease in humans. Methods of SNP detection include, but are not limited to, single-stranded conformation polymorphism (SSCP) and fluorescent SSCP (fSSCP) methods. In SSCP, oligonucleotide primers derived from mddt are used to amplify DNA using the polymerase chain reaction (PCR). The DNA may be derived, for example, from diseased or normal tissue, biopsy samples, bodily fluids, and the like. SNPs in the DNA cause differences in the secondary and tertiary structures of PCR products in single-stranded form, and these differences are detectable using gel electrophoresis in non-denaturing gels. In fSCCP, the oligonucleotide primers are fluorescently labeled, which allows detection of the amplimers in high-throughput equipment such as DNA sequencing machines. Additionally, sequence database analysis methods, termed in silico SNP (is SNP), are capable of identifying polymorphisms by comparing the sequences of individual overlapping DNA fragments which assemble into a common consensus sequence. These computer-based methods filter out sequence variations due to laboratory preparation of DNA and sequencing errors using statistical models and automated analyses of DNA sequence chromatograms. In the alternative, SNPs may be detected and characterized by mass spectrometry using, for example, the high throughput MASSARRAY system (Sequenom, Inc., San Diego Calif.).


[0164] DNA-based identification techniques are critical in forensic technology. DNA sequences taken from very small biological samples such as tissues, e.g., hair or skin, or body fluids, e.g., blood, saliva, semen, etc., can be amplified using, e.g., PCR, to identify individuals. (See, e.g., Erlich, H. (1992) PCR Technology, Freeman and Co., New York, N.Y.). Similarly, polynucleotides of the present invention can be used as polymorphic markers.


[0165] There is also a need for reagents capable of identifying the source of a particular tissue. Appropriate reagents can comprise, for example, DNA probes or primers prepared from the sequences of the present invention that are specific for particular tissues. Panels of such reagents can identify tissue by species and/or by organ type. In a similar fashion, these reagents can be used to screen tissue cultures for examination.


[0166] The polynucleotides of the present invention can also be used as molecular weight markers on nucleic acid gels or Southern blots, as diagnostic probes for the presence of a specific mRNA in a particular cell type, in the creation of subtracted cDNA libraries which aid in the discovery of novel polynucleotides, in selection and synthesis of oligomers for attachment to an array or other support, and as an antigen to elicit an immune response.


[0167] Disease Model Systems Using mddt


[0168] The mddt of the invention or their mammalian homologs may be “knocked out” in an animal model system using homologous recombination in embryonic stem (ES) cells. Such techniques are well known in the art and are useful for the generation of animal models of human disease. (See, e.g., U.S. Pat. No. 5,175,383 and U.S. Pat. No. 5,767,337.) For example, mouse ES cells, such as the mouse 129/SvJ cell line, are derived from the early mouse embryo and grown in culture. The ES cells are transformed with a vector containing the gene of interest disrupted by a marker gene, e.g., the neomycin phosphotransferase gene (neo; Capecchi, M. R. (1989) Science 244:1288-1292). The vector integrates into the corresponding region of the host genome by homologous recombination. Alternatively, homologous recombination takes place using the Cre-loxP system to knockout a gene of interest in a tissue- or developmental stage-specific manner (Marth, J. D. (1996) Clin. Invest. 97:1999-2002; Wagner, K. U. et al. (1997) Nucleic Acids Res. 25:4323-4330). Transformed ES cells are identified and microinjected into mouse cell blastocysts such as those from the C57BL/6 mouse strain. The blastocysts are surgically transferred to pseudopregnant dams, and the resulting chimeric progeny are genotyped and bred to produce heterozygous or homozygous strains. Transgenic animals thus generated may be tested with potential therapeutic or toxic agents.


[0169] The mddt of the invention may also be manipulated in vitro in ES cells derived from human blastocysts. Human ES cells have the potential to differentiate into at least eight separate cell lineages including endoderm, mesoderm, and ectodermal cell types. These cell lineages differentiate into, for example, neural cells, hematopoietic lineages, and cardiomyocytes (Thomson, J. A. et al. (1998) Science 282:1145-1147).


[0170] The mddt of the invention can also be used to create “knockin” humanized animals (pigs) or transgenic animals (mice or rats) to model human disease. With knockin technology, a region of mddt is injected into animal ES cells, and the injected sequence integrates into the animal cell genome. Transformed cells are injected into blastulae, and the blastulae are implanted as described above. Transgenic progeny or inbred lines are studied and treated with potential pharmaceutical agents to obtain information on treatment of a human disease. Alternatively, a mammal inbred to overexpress mddt, resulting, e.g., in the secretion of MDDT in its milk, may also serve as a convenient source of that protein (Janne, J. et al. (1998) Biotechnol. Annu. Rev. 4:55-74).


[0171] Screening Assays


[0172] MDDT encoded by polynucleotides of the present invention may be used to screen for molecules that bind to or are bound by the encoded polypeptides. The binding of the polypeptide and the molecule may activate (agonist), increase, inhibit (antagonist), or decrease activity of the polypeptide or the bound molecule. Examples of such molecules include antibodies, oligonucleotides, proteins (e.g., receptors), or small molecules.


[0173] Preferably, the molecule is closely related to the natural ligand of the polypeptide, e.g., a ligand or fragment thereof, a natural substrate, or a structural or functional mimetic. (See, Coligan et al., (1991) Current Protocols in Immunology 1(2): Chapter 5.) Similarly, the molecule can be closely related to the natural receptor to which the polypeptide binds, or to at least a fragment of the receptor, e.g., the active site. In either case, the molecule can be rationally designed using known techniques. Preferably, the screening for these molecules involves producing appropriate cells which express the polypeptide, either as a secreted protein or on the cell membrane. Preferred cells include cells from mammals, yeast, Drosophila, or E. coli. Cells expressing the polypeptide or cell membrane fractions which contain the expressed polypeptide are then contacted with a test compound and binding, stimulation, or inhibition of activity of either the polypeptide or the molecule is analyzed.


[0174] An assay may simply test binding of a candidate compound to the polypeptide, wherein binding is detected by a fluorophore, radioisotope, enzyme conjugate, or other detectable label. Alternatively, the assay may assess binding in the presence of a labeled competitor.


[0175] Additionally, the assay can be carried out using cell-free preparations, polypeptide/molecule affixed to a solid support, chemical libraries, or natural product mixtures. The assay may also simply comprise the steps of mixing a candidate compound with a solution containing a polypeptide, measuring polypeptide/molecule activity or binding, and comparing the polypeptide/molecule activity or binding to a standard.


[0176] Preferably, an ELISA assay using, e.g., a monoclonal or polyclonal antibody, can measure polypeptide level in a sample. The antibody can measure polypeptide level by either binding, directly or indirectly, to the polypeptide or by competing with the polypeptide for a substrate.


[0177] All of the above assays can be used in a diagnostic or prognostic context. The molecules discovered using these assays can be used to treat disease or to bring about a particular result in a patient (e.g., blood vessel growth) by activating or inhibiting the polypeptide/molecule. Moreover, the assays can discover agents which may inhibit or enhance the production of the polypeptide from suitably manipulated cells or tissues.


[0178] Transcript Imaging and Toxicological Testing


[0179] Another embodiment relates to the use of mddt to develop a transcript image of a tissue or cell type. A transcript image represents the global pattern of gene expression by a particular tissue or cell type. Global gene expression patterns are analyzed by quantifying the number of expressed genes and their relative abundance under given conditions and at a given time. (See Seilhamer et al., “Comparative Gene Transcript Analysis,” U.S. Pat. No. 5,840,484, expressly incorporated by reference herein.) Thus a transcript image may be generated by hybridizing the polynucleotides of the present invention or their complements to the totality of transcripts or reverse transcripts of a particular tissue or cell type. In one embodiment, the hybridization takes place in high-throughput format, wherein the polynucleotides of the present invention or their complements comprise a subset of a plurality of elements on a microarray. The resultant transcript image would provide a profile of gene activity pertaining to disease detection and treatment molecules.


[0180] Transcript images which profile mddt expression may be generated using transcripts isolated from tissues, cell lines, biopsies, or other biological samples. The transcript image may thus reflect mddt expression in vivo, as in the case of a tissue or biopsy sample, or in vitro, as in the case of a cell line.


[0181] Transcript images which profile mddt expression may also be used in conjunction with in vitro model systems and preclinical evaluation of pharmaceuticals, as well as toxicological testing of industrial and naturally-occurring environmental compounds. All compounds induce characteristic gene expression patterns, frequently termed molecular fingerprints or toxicant signatures, which are indicative of mechanisms of action and toxicity (Nuwaysir, E. F. et al. (1999) Mol. Carcinog. 24:153-159; Steiner, S. and Anderson, N. L. (2000) Toxicol. Lett. 112-113:467-71, expressly incorporated by reference herein). If a test compound has a signature similar to that of a compound with known toxicity, it is likely to share those toxic properties. These fingerprints or signatures are most useful and refined when they contain expression information from a large number of genes and gene families. Ideally, a genome-wide measurement of expression provides the highest quality signature. Even genes whose expression is not altered by any tested compounds are important as well, as the levels of expression of these genes are used to normalize the rest of the expression data. The normalization procedure is useful for comparison of expression data after treatment with different compounds. While the assignment of gene function to elements of a toxicant signature aids in interpretation of toxicity mechanisms, knowledge of gene function is not necessary for the statistical matching of signatures which leads to prediction of toxicity. (See, for example, Press Release 00-02 from the National Institute of Environmental Health Sciences, released Feb. 29, 2000, available at http://www.niehs.nih.gov/oc/news/toxchip.htm.) Therefore, it is important and desirable in toxicological screening using toxicant signatures to include all expressed gene sequences.


[0182] In one embodiment, the toxicity of a test compound is assessed in treating a biological sample containing nucleic acids with the test compound. Nucleic acids that are expressed in the treated biological sample are hybridized with one or more probes specific to the polynucleotides of the present invention, so that transcript levels corresponding to the polynucleotides of the present invention may be quantified. The transcript levels in the treated biological sample are compared with levels in an untreated biological sample. Differences in the transcript levels between the two samples are indicative of a toxic response caused by the test compound in the treated sample.


[0183] Another particular embodiment relates to the use of MDDT encoded by polynucleotides of the present invention to analyze the proteome of a tissue or cell type. The term proteome refers to the global pattern of protein expression in a particular tissue or cell type. Each protein component of a proteome can be subjected individually to further analysis. Proteome expression patterns, or profiles, are analyzed by quantifying the number of expressed proteins and their relative abundance under given conditions and at a given time. A profile of a cell's proteome may thus be generated by separating and analyzing the polypeptides of a particular tissue or cell type. In one embodiment, the separation is achieved using two-dimensional gel electrophoresis, in which proteins from a sample are separated by isoelectric focusing in the first dimension, and then according to molecular weight by sodium dodecyl sulfate slab gel electrophoresis in the second dimension (Steiner and Anderson, supra). The proteins are visualized in the gel as discrete and uniquely positioned spots, typically by staining the gel with an agent such as Coomassie Blue or silver or fluorescent stains. The optical density of each protein spot is generally proportional to the level of the protein in the sample. The optical densities of equivalently positioned protein spots from different samples, for example, from biological samples either treated or untreated with a test compound or therapeutic agent, are compared to identify any changes in protein spot density related to the treatment. The proteins in the spots are partially sequenced using, for example, standard methods employing chemical or enzymatic cleavage followed by mass spectrometry. The identity of the protein in a spot may be determined by comparing its partial sequence, preferably of at least 5 contiguous amino acid residues, to the polypeptide sequences of the present invention. In some cases, further sequence data may be obtained for definitive protein identification.


[0184] A proteomic profile may also be generated using antibodies specific for MDDT to quantify the levels of MDDT expression. In one embodiment, the antibodies are used as elements on a microarray, and protein expression levels are quantified by exposing the microarray to the sample and detecting the levels of protein bound to each array element (Lueking, A. et al. (1999) Anal. Biochem. 270:103-11; Mendoze, L. G. et al. (1999) Biotechniques 27:778-88). Detection may be performed by a variety of methods known in the art, for example, by reacting the proteins in the sample with a thiol- or amino-reactive fluorescent compound and detecting the amount of fluorescence bound at each array element.


[0185] Toxicant signatures at the proteome level are also useful for toxicological screening, and should be analyzed in parallel with toxicant signatures at the transcript level. There is a poor correlation between transcript and protein abundances for some proteins in some tissues (Anderson. N. L. and Seilhamer, J. (1997) Electrophoresis 18:533-537), so proteome toxicant signatures may be useful in the analysis of compounds which do not significantly affect the transcript image, but which alter the proteomic profile. In addition, the analysis of transcripts in body fluids is difficult, due to rapid degradation of mRNA, so proteomic profiling may be more reliable and informative in such cases.


[0186] In another embodiment, the toxicity of a test compound is assessed by treating a biological sample containing proteins with the test compound. Proteins that are expressed in the treated biological sample are separated so that the amount of each protein can be quantified. The amount of each protein is compared to the amount of the corresponding protein in an untreated biological sample. A difference in the amount of protein between the two samples is indicative of a toxic response to the test compound in the treated sample. Individual proteins are identified by sequencing the amino acid residues of the individual proteins and comparing these partial sequences to the MDDT encoded by polynucleotides of the present invention.


[0187] In another embodiment, the toxicity of a test compound is assessed by treating a biological sample containing proteins with the test compound. Proteins from the biological sample are incubated with antibodies specific to the MDDT encoded by polynucleotides of the present invention. The amount of protein recognized by the antibodies is quantified. The amount of protein in the treated biological sample is compared with the amount in an untreated biological sample. A difference in the amount of protein between the two samples is indicative of a toxic response to the test compound in the treated sample.


[0188] Transcript images may be used to profile mddt expression in distinct tissue types. This process can be used to determine disease detection and treatment molecule activity in a particular tissue type relative to this activity in a different tissue type. Transcript images may be used to generate a profile of mddt expression characteristic of diseased tissue. Transcript images of tissues before and after treatment may be used for diagnostic purposes, to monitor the progression of disease, and to monitor the efficacy of drug treatments for diseases which affect the activity of disease detection and treatment molecules.


[0189] Transcript images of cell lines can be used to assess disease detection and treatment molecule activity and/or to identify cell lines that lack or misregulate this activity. Such cell lines may then be treated with pharmaceutical agents, and a transcript image following treatment may indicate the efficacy of these agents in restoring desired levels of this activity. A similar approach may be used to assess the toxicity of pharmaceutical agents as reflected by undesirable changes in disease detection and treatment molecule ity. Candidate pharmaceutical agents may be evaluated by comparing their associated transcript images with those of pharmaceutical agents of known effectiveness.


[0190] Antisense Molecules


[0191] The polynucleotides of the present invention are useful in antisense technology. Antisense technology or therapy relies on the modulation of expression of a target protein through the specific binding of an antisense sequence to a target sequence encoding the target protein or directing its expression. (See, e.g., Agrawal, S., ed. (1996) Antisense Therapeutics, Humana Press Inc. Totawa N.J.; Alama, A. et al. (1997) Pharmacol. Res. 36(3): 171-178; Crooke, S. T. (1997) Adv. Pharmacol. 40:1-49; Sharma, H. W. and R. Narayanan (1995) Bioessays 17(12):1055-1063; and Lavrosky, Y. et al. (1997) Biochem. Mol. Med. 62(1):11-22.) An antisense sequence is a polynucleotide sequence capable of specifically hybridizing to at least a portion of the target sequence. Antisense sequences bind to cellular mRNA and/or genomic DNA, affecting translation and/or transcription. Antisense sequences can be DNA, RNA, or nucleic acid mimics and analogs. (See, e.g., Rossi, J. J. et al. (1991) Antisense Res. Dev. 1(3):285-288; Lee, R. et al. (1998) Biochemistry 37(3):900-1010; Pardridge, W. M. et al. (1995) Proc. Natl. Acad. Sci. USA 92(12):5592-5596; and Nielsen, P. E. and Haaima, G. (1997) Chem. Soc. Rev. 96:73-78.) Typically, the binding which results in modulation of expression occurs through hybridization or binding of complementary base pairs. Antisense sequences can also bind to DNA duplexes through specific interactions in the major groove of the double helix.


[0192] The polynucleotides of the present invention and fragments thereof can be used as antisense sequences to modify the expression of the polypeptide encoded by mddt. The antisense sequences can be produced ex vivo, such as by using any of the ABI nucleic acid synthesizer series (Applied Biosystems) or other automated systems known in the art. Antisense sequences can also be produced biologically, such as by transforming an appropriate host cell with an expression vector containing the sequence of interest. (See, e.g., Agrawal, supra.)


[0193] In therapeutic use, any gene delivery system suitable for introduction of the antisense sequences into appropriate target cells can be used. Antisense sequences can be delivered intracellularly in the form of an expression plasmid which, upon transcription, produces a sequence complementary to at least a portion of the cellular sequence encoding the target protein. (See, e.g., Slater, J. E., et al. (1998) J. Allergy Clin. Immunol. 102(3):469-475; and Scanlon, K. J., et al. (1995) 9(13): 1288-1296.) Antisense sequences can also be introduced intracellularly through the use of viral vectors, such as retrovirus and adeno-associated virus vectors. (See, e.g., Miller, A. D. (1990) Blood 76:271; Ausubel, F. M. et al. (1995) Current Protocols in Molecular Biology, John Wiley & Sons, New York N.Y.; Uckert, W. and W. Walther (1994) Pharmacol. Ther. 63(3):323-347.) Other gene delivery mechanisms include liposome-derived systems, artificial viral envelopes, and other systems known in the art. (See, e.g., Rossi, 1995) Br. Med. Bull. 51(1):217-225; Boa J. et al. (1998) J. Pharm. Sci. 87(11):1308-1315; and Morris, M. C. et al. (1997) Nucleic Acids Res. 25(14):2730-2736.)


[0194] Expression


[0195] In order to express a biologically active MDDT, the nucleotide sequences encoding MDDT or fragments thereof may be inserted into an appropriate expression vector. i.e., a vector which contains the necessary elements for transcriptional and translational control of the inserted coding sequence in a suitable host. Methods which are well known to those skilled in the art may be used to construct expression vectors containing sequences encoding MDDT and appropriate transcriptional and translational control elements. These methods include in vitro recombinant DNA techniques, synthetic techniques, and in vivo genetic recombination. (See, e.g., Sambrook, supra, Chapters 4, 8, 16, and 17; and Ausubel, supra, Chapters 9, 10, 13, and 16.)


[0196] A variety of expression vector/host systems may be utilized to contain and express sequences encoding MDDT. These include, but are not limited to, microorganisms such as bacteria transformed with recombinant bacteriophage, plasmid, or cosmid DNA expression vectors; yeast transformed with yeast expression vectors; insect cell systems infected with viral expression vectors (e.g., baculovirus); plant cell systems transformed with viral expression vectors (e.g., cauliflower mosaic virus, CaMV, or tobacco mosaic virus, TMV) or with bacterial expression vectors (e.g., Ti or pBR322 plasmids); or animal (mammalian) cell systems. (See, e.g., Sambrook, supra; Ausubel, 1995, supra, Van Heeke, G. and S. M. Schuster (1989) J. Biol. Chem. 264:5503-5509; Bitter, G. A. et al. (1987) Methods Enzymol. 153:516-544; Scorer, C. A. et al. (1994) Bio/Technology 12:181-184; Engelhard, E. K. et al. (1994) Proc. Natl. Acad. Sci. USA 91:3224-3227; Sandig, V. et al. (1996) Hum. Gene Ther. 7:1937-1945; Takamatsu, N. (1987) EMBO J. 6:307-311; Coruzzi, G. et al. (1984) EMBO J. 3:1671-1680; Broglie, R. et al. (1984) Science 224:838-843; Winter, J. et al. (1991) Results Probl. Cell Differ. 17:85-105; The McGraw Hill Yearbook of Science and Technology (1992) McGraw Hill, New York N.Y., pp. 191-196; Logan, J. and T. Shenk (1984) Proc. Natl. Acad. Sci. USA 81:3655-3659; and Harrington, J. J. et al. (1997) Nat. Genet. 15:345-355.) Expression vectors derived from retroviruses, adenoviruses, or herpes or vaccinia viruses, or from various bacterial plasmids, may be used for delivery of nucleotide sequences to the targeted organ, tissue, or cell population. (See, e.g., Di Nicola, M. et al. (1998) Cancer Gen. Ther. 5(6):350-356: Yu, M. et al., (1993) Proc. Natl. Acad. Sci. USA 90(13):6340-6344; Buller, R. M. et al. (1985) Nature 317(6040):813-815; McGregor, D. P. et al. (1994) Mol. Immunol. 31(3):219-226; and Verma, I. M. and N. Somia (1997) Nature 389:239-242.) The invention is not limited by the host cell employed.


[0197] For long term production of recombinant proteins in mammalian systems, stable expression of MDDT in cell lines is preferred. For example, sequences encoding MDDT can be transformed into cell lines using expression vectors which may contain viral origins of relation and/or endogenous expression elements and a selectable marker gene on the same or on a separate vector. Any number of selection systems may be used to recover transformed cell lines. (See, e.g., Wigler, M. et al. (1977) Cell 11:223-232; Lowy, I. et al. (1980) Cell 22:817-823.; Wigler, M. et al. (1980) Proc. Natl. Acad. Sci. USA 77:3567-3570; Colbere-Garapin, F. et al. (1981) J. Mol. Biol. 150:1-14; Hartman, S. C. and R. C. Mulligan (1988) Proc. Natl. Acad. Sci. USA 85:8047-8051; Rhodes, C. A. (1995) Methods Mol. Biol. 55:121-131.)


[0198] Therapeutic Uses of mddt


[0199] The mddt of the invention may be used for somatic or germline gene therapy. Gene therapy may be performed to (i) correct a genetic deficiency (e.g., in the cases of severe combined immunodeficiency (SCID)-X1 disease characterized by X-linked inheritance (Cavazzana-Calvo, M. et al. (2000) Science 288:669-672), severe combined immunodeficiency syndrome associated with an inherited adenosine deaminase (ADA) deficiency (Blaese, R. M. et al. (1995) Science 270:475-480; Bordignon, C. et al. (1995) Science 270:470-475), cystic fibrosis (Zabner, J. et al. (1993) Cell 75:207-216; Crystal, R. G. et al. (1995) Hum. Gene Therapy 6:643-666; Crystal, R. G. et al. (1995) Hum. Gene Therapy 6:667-703), thalassemias, familial hypercholesterolemia, and hemophilia resulting from Factor VIII or Factor IX deficiencies (Crystal, R. G. (1995) Science 270:404-410; Verma, I. M. and Somia, N. (1997) Nature 389:239-242)), (ii) express a conditionally lethal gene product (e.g., in the case of cancers which result from unregulated cell proliferation), or (iii) express a protein which affords protection against intracellular parasites (e.g., against human retroviruses, such as human immunodeficiency virus (HIV) (Baltimore. D. (1988) Nature 335:395-396; Poeschla, E. et al. (1996) Proc. Natl. Acad. Sci. USA. 93:11395-11399), hepatitis B or C virus (HBV, HCV); fungal parasites, such as Candida albicans and Paracoccidioides brasiliensis; and protozoan parasites such as Plasmodium falciparum and Trypanosoma cruzi). In the case where a genetic deficiency in mddt expression or regulation causes disease, the expression of mddt from an appropriate population of transduced cells may alleviate the clinical manifestations caused by the genetic deficiency.


[0200] In a further embodiment of the invention, diseases or disorders caused by deficiencies in mddt are treated by constructing mammalian expression vectors comprising mddt and introducing these vectors by mechanical means into mddt-deficient cells. Mechanical transfer technologies for use with cells in vivo or ex vitro include (i) direct DNA microinjection into individual cells, (ii) ballistic gold particle delivery, (iii) liposome-mediated transfection, (iv) receptor-mediated gene transfer, and (v) the use of DNA transposons (Morgan, R. A. and Anderson, W. F. (1993) Annu. Rev. Biochem. 62:191-217; Ivics, Z. (1997) Cell 91:501-510; Boulay, J-L. and Récipon, H. (1998) Curr. Opin. Biotechnol. 9:445-450).


[0201] Expression vector that may be effective for the expression of may include, but are not limited to, the PCDNA 3.1, EPITAG, PRCCMV2, PREP, PVAX vectors (Invitrogen, Carlsbad Calif.). PCMV-SCRIPT, PCMV-TAG, PEGSH/PERV (Stratagene, La Jolla Calif.), and PTET-OFF, PTET-ON, PTRE2, PTRE2-LUC, PTK-HYG (Clontech. Palo Alto Calif.). The mddt of the invention may be expressed using (i) a constitutively active promoter, (e.g., from cytomegalovirus (CMV), Rous sarcoma virus (RSV), SV40 virus, thymidine kinase (TK), or β-actin genes), (ii) an inducible promoter (e.g., the tetracycline-regulated promoter (Gossen, M. and Bujard, H. (1992) Proc. Natl. Acad. Sci. U.S.A. 89:5547-5551; Gossen, M. et al., (1995) Science 268:1766-1769; Rossi, F. M. V. and Blau, H. M. (1998) Curr. Opin. Biotechnol. 9:451-456), commercially available in the T-REX plasmid (Invitrogen); the ecdysone-inducible promoter (available in the plasmids PVGRXR and PIND: Invitrogen); the FK506/rapamycin inducible promoter; or the RU486/mifepristone inducible promoter (Rossi, F. M. V. and Blau, H. M. supra), or (iii) a tissue-specific promoter or the native promoter of the endogenous gene encoding MDDT from a normal individual.


[0202] Commercially available liposome transformation kits (e.g., the PERFECT LIPID TRANSFECTION KIT, available from Invitrogen) allow one with ordinary skill in the art to deliver polynucleotides to target cells in culture and require minimal effort to optimize experimental parameters. In the alternative, transformation is performed using the calcium phosphate method (Graham, F. L. and Eb, A. J. (1973) Virology 52:456-467), or by electroporation (Neumann, E. et al. (1982) EMBO J. 1:841-845). The introduction of DNA to primary cells requires modification of these standardized mammalian transfection protocols.


[0203] In another embodiment of the invention, diseases or disorders caused by genetic defects with respect to mddt expression are treated by constructing a retrovirus vector consisting of (i) mddt under the control of an independent promoter or the retrovirus long terminal repeat (LTR) promoter, (ii) appropriate RNA packaging signals, and (iii) a Rev-responsive element (RRE) along with additional retrovirus cis-acting RNA sequences and coding sequences required for efficient vector propagation. Retrovirus vectors (e.g., PFB and PFBNEO) are commercially available (Stratagene) and are based on published data (Riviere, I. et al. (1995) Proc. Natl. Acad. Sci. U.S.A. 92:6733-6737), incorporated by reference herein. The vector is propagated in an appropriate vector producing cell line (VPCL) that expresses an envelope gene with a tropism for receptors on the target cells or a promiscuous envelope protein such as VSVg (Armentano, D. et al. (1987) J. Virol. 61:1647-1650; Bender, M. A. et al. (1987) J. Virol. 61:1639-1646; Adam, M. A. and Miller, A. D. (1988) J. Virol. 62:3802-3806; Dull, T. et al. (1998) J. Virol. 72:8463-8471; Zufferey, R. et al. (1998) J. Virol. 72:9873-9880). U.S. Pat. No. 5,910,434 to Rigg (“Method for obtaining retrovirus packaging cell lines producing high transducing efficiency retroviral supernatant”) discloses a method for obtaining retrovirus packaging cell lines and is hereby incorporated by reference. Propagation of retrovirus vectors, transduction of a population of cells (e.g. CD4+T-cells), and the return of transduced to a patient are procedures well known to persons skilled in the art of gene therapy and have been well documented (Ranga, U. et al. (1997) J. Virol. 71:7020-7029; Bauer, G. et al. (1997) Blood 89:2259-2267; Bonyhadi, M. L. (1997) J. Virol. 71:47074716; Ranga, U. et al. (1998) Proc. Natl. Acad. Sci. U.S.A. 95:1201-1206; Su, L. (1997) Blood 89:2283-2290).


[0204] In the alternative, an adenovirus-based gene therapy delivery system is used to deliver mddt to cells which have one or more genetic abnormalities with respect to the expression of mddt. The construction and packaging of adenovirus-based vectors are well known to those with ordinary skill in the art. Replication defective adenovirus vectors have proven to be versatile for importing genes encoding immunoregulatory proteins into intact islets in the pancreas (Csete, M. E. et al. (1995) Transplantation 27:263-268). Potentially useful adenoviral vectors are described in U.S. Pat. No. 5,707,618 to Armentano (“Adenovirus vectors for gene therapy”), hereby incorporated by reference. For adenoviral vectors, see also Antinozzi, P. A. et al. (1999) Annu. Rev. Nutr. 19:511-544 and Verma, I. M. and Somia, N. (1997) Nature 18:389:239-242, both incorporated by reference herein.


[0205] In another alternative, a herpes-based, gene therapy delivery system is used to deliver mddt to target cells which have one or more genetic abnormalities with respect to the expression of mddt. The use of herpes simplex virus (HSV)-based vectors may be especially valuable for introducing mddt to cells of the central nervous system, for which HSV has a tropism. The construction and packaging of herpes-based vectors are well known to those with ordinary skill in the art. A replication-competent herpes simplex virus (HSV) type 1-based vector has been used to deliver a reporter gene to the eyes of primates (Liu, X. et al. (1999) Exp. Eye Res. 169:385-395). The construction of a HSV-1 virus vector has also been disclosed in detail in U.S. Pat. No. 5,804,413 to DeLuca (“Herpes simplex virus strains for gene transfer”), which is hereby incorporated by reference. U.S. Pat. No. 5,804,413 teaches the use of recombinant HSV d92 which consists of a genome containing at least one exogenous gene to be transferred to a cell under the control of the appropriate promoter for purposes including human gene therapy. Also taught by this patent are the construction and use of recombinant HSV strains deleted for ICP4, ICP27 and ICP22. For HSV vectors, see also Goins, W. F. et al. 1999 J. Virol. 73:519-532 and Xu, H. et al., (1994) Dev. Biol. 163:152-161, hereby incorporated by reference. The manipulation of cloned herpesvirus sequences, the generation of recombinant virus following the transfection of multiple plasmids containing different segments of the large herpesvirus genomes, the growth and propagation of herpesvirus, and the infection of cells with herpesvirus are techniques well known to those of ordinary skill in the art.


[0206] In another alternative, an alphavirus (positive, single-stranded RNA virus) vector is used to deliver mddt to target cells. The biology of the prototypic alphavirus, Semliki Forest Virus (SFV), has been studied extensively and gene transfer vectors have been based on the SFV genome (Garoff, H. and Li, K-J. (1998) Current Biotech. 9:464-469). During alphavirus RNA replication, a subgenomic RNA is generated that normally encodes the viral capsid proteins. This subgenomic RNA replicates to higher levels than the full-length genomic RNA, resulting in the overproduction of capsid proteins relative to the viral proteins with enzymatic activity (e.g., protease and polymerase). Similarly, inserting mddt into the alphavirus genome in place of the capsid-coding region results in the production of a large number of mddt RNAs and the synthesis of high levels of MDDT in vector transduced cells. While alphavirus infection is typically associated with cell lysis within a few days, the ability to establish a persistent infection in hamster normal kidney cells (BHK-21) with a variant of Sindbis virus (SIN) indicates that the lytic replication of alphaviruses can be altered to suit the needs of the gene therapy application (Dryga, S. A. et al. (1997) Virology 228:74-83). The wide host range of alphaviruses will allow the introduction of mddt into a variety of cell types. The specific transduction of a subset of cells in a population may require the sorting of cells prior to transduction. The methods of manipulating infectious cDNA clones of alphaviruses, performing alphavirus cDNA and RNA transfections, and performing alphavirus infections, are well known to those with ordinary skill in the art.


[0207] Antibodies


[0208] Anti-MDDT antibodies may be used to analyze protein expression levels. Such antibodies include, but are not limited to, polyclonal, monoclonal, chimeric, single chain, and Fab fragments. For descriptions of and protocols of antibody technologies, see, e.g., Pound J. D. (1998) Immunochemical Protocols, Humana Press, Totowa, N.J.


[0209] The amino acid sequence encoded by the mddt of the Sequence Listing may be analyzed by appropriate software (e.g., LASERGENE NAVIGATOR software, DNASTAR) to determine regions of high immunogenicity. The optimal sequences for immunization are selected from the C-terminus, the N-terminus, and those intervening, hydrophilic regions of the polypeptide which are likely to be exposed to the external environment when the polypeptide is in its natural conformation. Analysis used to select appropriate epitopes is also described by Ausubel (1997, supra, Chapter 11.7). Peptides used for antibody induction do not need to have biological activity; however, they must be antigenic. Peptides used to induce specific antibodies may have an amino acid sequence consisting of at least five amino acids, preferably at least 10 amino acids, and most preferably at least 15 amino acids. A peptide which mimics an antigenic fragment of the natural polypeptide may be fused with another protein such as keyhole hemolimpet cyanin (KLH; Sigma, St. Louis Mo.) for antibody production. A peptide encompassing an antigenic region may be expressed from an mddt, synthesized as described above, or purified from human cells.


[0210] Procedures well known in the art may be used for the production of antibodies. Various hosts including mice, goats, and rabbits, may be immunized by injection with peptide. Depending on the host species, various adjuvants may be used to increase immunological response.


[0211] In one procedure, peptides about 15 residues in length may be synthesized using an ABI 431 A peptide synthesizer (Applied Biosystems) using fmoc-chemistry and coupled to KLH (Sigma) by reaction with M-maleimidobenzoyl-N-hydroxysuccinimide ester (Ausubel, 1995, supra). Rabbits are immunized with the peptide-KLH complex in complete Freund's adjuvant. The resulting antisera are tested for antipeptide activity by binding the peptide to plastic, blocking with 1% bovine serum albumin (BSA), reacting with rabbit antisera, washing, and reacting with radioiodinated goat anti-rabbit IgG. Antisera with antipeptide activity are tested for anti-MDDT activity using protocols well known in the art, including ELISA, radioimmunoassay (RIA), and immunoblotting.


[0212] In another procedure, isolated and purified peptide may be used to immunize mice (about 100 μg of peptide) or rabbits (about 1 mg of peptide). Subsequently, the peptide is radioiodinated and used to screen the immunized animals' B-lymphocytes for production of antipeptide antibodies. Positive cells are then used to produce hybridomas using standard techniques. About 20 mg of peptide is sufficient for labeling and screening several thousand clones. Hybridomas of interest are detected by screening with radioiodinated peptide to identify those fusions producing peptide-specific monoclonal antibody. In a typical protocol, wells of a multi-well plate (FAST, Becton-Dickinson, Palo Alto, Calif.) are coated with affinity-purified, specific rabbit-anti-mouse (or suitable anti-species IgG) antibodies at 10 mg/ml. The coated wells are blocked with 1% BSA and washed and exposed to supernatants from hybridomas. After incubation, the wells are exposed to radiolabeled peptide at 1 mg/ml.


[0213] Clones producing antibodies bind a quantity of labeled peptide that is detectable above background. Such clones are expanded and subjected to 2 cycles of cloning. Cloned hybridomas are injected into pristane-treated mice to produce ascites, and monoclonal antibody is purified from the ascitic fluid by affinity chromatography on protein A (Amersham Pharmacia Biotech). Several procedures for the production of monoclonal antibodies, including in vitro production, are described in Pound (supra). Monoclonal antibodies with antipeptide activity are tested for anti-MDDT activity using protocols well known in the art, including ELISA, RIA, and immunoblotting.


[0214] Antibody fragments containing specific binding sites for an epitope may also be generated. For example, such fragments include, but are not limited to, the F(ab′)2 fragments produced by pepsin digestion of the antibody molecule, and the Fab fragments generated by reducing the disulfide bridges of the F(ab′)2 fragments. Alternatively, construction of Fab expression libraries in filamentous bacteriophage allows rapid and easy identification of monoclonal fragments with desired specificity (Pound, supra, Chaps. 45-47). Antibodies generated against polypeptide encoded by mddt can be used to purify and characterize full-length MDDT protein and its activity, binding partners, etc.


[0215] Assays Using Antibodies


[0216] Anti-MDDT antibodies may be used in assays to quantify the amount of MDDT found in a particular human cell. Such assays include methods utilizing the antibody and a label to detect expression level under normal or disease conditions. The peptides and antibodies of the invention may be used with or without modification or labeled by joining them, either covalently or noncovalently, with a reporter molecule.


[0217] Protocols for detecting and measuring protein expression using either polyclonal or monoclonal antibodies are well known in the art. Examples include ELISA, RIA, and fluorescent activated cell sorting (FACS). Such immunoassays typically involve the formation of complexes between the MDDT and its specific antibody and the measurement of such complexes. These and other assays are described in Pound (supra).


[0218] Without further elaboration, it is believed that one skilled in the art can, using the preceding description, utilize the present invention to its fullest extent. The following preferred specific embodiments are, therefore, to be construed as merely illustrative, and not limitative of the remainder of the disclosure in any way whatsoever.


[0219] The disclosures of all patents, applications, and publications mentioned above and below, including U.S. Serial No. 60/230,517, U.S. Serial No. 60/230,599, U.S. Serial No. 60/230,514, U.S. Serial No. 60/231,167, U.S. Serial No. 60/230,598, U.S. Serial No. 60/230,988, U.S. Serial No. 60/230,518, U.S. Serial No. 60/230,515, U.S. Serial No. 60/229,751, U.S. Serial No. 60/230,610, U.S. Serial No. 60/229,749, U.S. Serial No. 60/229,750, U.S. Serial No. 60/230,597, U.S. Serial No. 60/230,505, U.S. Serial No. 60/231,163, U.S. Serial No. 60/229,747, U.S. Serial No. 60/229,748, U.S. Serial No. 60/230,583, U.S. Serial No. 60/230,519, U.S. Serial No. 60/230,595, U.S. Serial No. 60/230,865, U.S. Serial No. 60/230,989, and U.S. Serial No. 60/230,951, are hereby expressly incorporated by reference.



EXAMPLES

[0220] I. Construction of cDNA Libraries


[0221] RNA was purchased from CLONTECH Laboratories, Inc. (Palo Alto Calif.) or isolated from various tissues. Some tissues were homogenized and lysed in guanidinium isothiocyanate, while others were homogenized and lysed in phenol or in a suitable mixture of denaturants, such as TRIZOL (Life Technologies), a monophasic solution of phenol and guanidine isothiocyanate. The resulting lysates were centrifuged over CsCl cushions or extracted with chloroform. RNA was precipitated with either isopropanol or sodium acetate and ethanol, or by other routine methods.


[0222] Phenol extraction and precipitation of RNA were repeated as necessary to increase RNA purity. In most cases. RNA was treated with DNase. For most libraries, poly(A+) RNA was isolated using oligo d(T)coupled magnetic particles (Promega Corporation, Omega), Madison Wis.), OLIGOTEX latex particles (QIAGEN, Inc. (QIAGEN), Valencia Calif.), or an OLIGOTEX mRNA purification kit (QIAGEN). Alternatively, RNA was isolated directly from tissue lysates using other RNA isolation kits, e.g., the POLY(A)PURE mRNA purification kit (Ambion, Inc. Austin Tex.).


[0223] In some cases, Stratagene was provided with RNA and constructed the corresponding cDNA libraries. Otherwise, cDNA was synthesized and cDNA libraries were constructed with the UNIZAP vector system (Stratagene Cloning Systems, Inc. (Stratagene), La Jolla Calif.) or SUPERSCRIPT plasmid system (Life Technologies), using the recommended procedures or similar methods known in the art. (See, e.g., Ausubel, 1997, supra, Chapters 5.1 through 6.6.) Reverse transcription was initiated using oligo d(T) or random primers. Synthetic oligonucleotide adapters were ligated to double stranded cDNA, and the cDNA was digested with the appropriate restriction enzyme or enzymes. For most libraries, the cDNA was size-selected (300-1000 bp) using SEPHACRYL S1000, SEPHAROSE CL2B, or SEPHAROSE CL4B column chromatography (Amersham Pharmacia Biotech) or preparative agarose gel electrophoresis. cDNAs were ligated into compatible restriction enzyme sites of the polylinker of a suitable plasmid, e.g. PBLUESCRIPT plasmid (Stratagene), PSPORT1 plasmid (Life Technologies), PCDNA2.1 plasmid (Invitrogen, Carlsbad Calif.), PBK-CMV plasmid (Stratagene), or pINCY (Incyte Genomics, Palo Alto Calif.), or derivatives thereof. Recombinant plasmids were transformed into competent E. coli cells including XL1-Blue, XL1-BlueMRF, or SOLR from Stratagene or DH5α, DH10B, or ElectroMAX DH10B from Life Technologies.


[0224] II. Isolation of cDNA Clones


[0225] Plasmids were recovered from host cells by in vivo excision using the UNIZAP vector system (Stratagene) or by cell lysis. Plasmids were purified using at least one of the following: the Magic or WIZARD Minipreps DNA purification system (Promega); the AGTC Miniprep purification kit (Edge BioSystems, Gaithersburg Md.); and the QIAWELL 8, QIAWELL 8 Plus, and QIAWELL 8 Ultra plasmid purification systems or the R.E.A.L. PREP 96 plasmid purification kit (QIAGEN). Following precipitation, plasmids were resuspended in 0.1 ml of distilled water and stored, with or without lyophilization, at 4° C.


[0226] Alternatively, plasmid DNA was amplified from host cell lysates using direct link PCR in a high-throughput format. (Rao, V. B. (1994) Anal. Biochem. 216:1-14.) Host cell lysis and thermal cycling steps were carried out in a single reaction mixture. Samples were processed and stored in 384-well plates, and the concentration of amplified plasmid DNA was quantified fluorometrically using PICOGREEN dye (Molecular Probes, Inc. (Molecular Probes), Eugene Oreg.) and a FLUOROSKAN II fluorescence scanner (Labsystems Oy, Helsinki, Finland).


[0227] III. Sequencing and Analysis


[0228] cDNA sequencing reactions were processed using standard methods or high-throughput instrumentation such as the ABI CATALYST 800 thermal cycler (Applied Biosystems) or the PTC-200 thermal cycler (MJ Research) in conjunction with the HYDRA microdispenser (Robbins Scientific Corp., Sunnyvale Calif.) or the MICROLAB 2200 liquid transfer system (Hamilton). cDNA sequencing reactions were prepared using reagents provided by Amersham Pharmacia Biotech or supplied in ABI sequencing kits such as the ABI PRISM BIGDYE Terminator cycle sequencing ready reaction kit (Applied Biosystems). Electrophoretic separation of cDNA sequencing reactions and detection of labeled polynucleotides were carried out using the MEGABACE 1000 DNA sequencing system (Molecular Dynamics); the ABI PRISM 373 or 377 sequencing system (Applied Biosystems) in conjunction with standard ABI protocols and base calling software; or other sequence analysis systems known in the art. Reading frames within the cDNA sequences were identified using standard methods (reviewed in Ausubel, 1997, supra, Chapter 7.7). Some of the cDNA sequences were selected for extension using the techniques disclosed in Example VIII.


[0229] IV. Assembly and Analysis of Sequences


[0230] Component sequences from chromatograms were subject to PHRED analysis and assigned a quality score. The sequences having at least a required quality score were subject to various pre-processing editing pathways to eliminate, e.g., low quality 3′ ends, vector and linker sequences, polyA tails, Alu repeats, mitochondrial and ribosomal sequences, bacterial contamination sequences, and sequences smaller than 50 base pairs. In particular, low-information sequences and repetitive elements (e.g., dinucleotide repeats, Alu repeats, etc.) were replaced by “n's”, or masked, to prevent spurious matches.


[0231] Processed sequences were then subject to assembly procedures in which the sequences were assigned to gene bins (bins). Each sequence could only belong to one bin. Sequences in each gene bin were assembled to produce consensus sequences (templates). Subsequent new sequences were added to existing bins using BLASTn (v. 1.4 WashU) and CROSSMATCH. Candidate pairs were identified as all BLAST hits having a quality score greater than or equal to 150. Alignments of at least 82% local identity were accepted into the bin. The component sequences from each bin were assembled using a version of PHRAP. Bins with several overlapping component sequences were assembled using DEEP PHRAP. The orientation (sense or antisense) of each assembled template was determined based on the number and orientation of its component sequences. Template sequences as disclosed in the sequence listing correspond to sense strand sequences (the “forward” reading frames), to the best determination. The complementary (antisense) strands are inherently disclosed herein. The component sequences which were used to assemble each template consensus sequence are listed in Table 5, along with their positions along the template nucleotide sequences.


[0232] Bins were compared against each other and those having local similarity of at least 82% were combined and reassembled. Reassembled bins having templates of insufficient overlap (less than 95% local identity) were re-split. Assembled templates were also subject to analysis by STITCHER/EXON MAPPER algorithms which analyze the probabilities of the presence of splice variants, alternatively spliced exons, splice junctions, differential expression of alternative spliced genes across tissue types or disease states, etc. These resulting bins were subject to several rounds of the above assembly procedures.


[0233] Once gene bins were generated based upon sequence alignments, bins were clone joined based upon clone information. If the 5′sequence of one clone was present in one bin and the 3′ sequence from the same clone was present in a different bin, it was likely that the two bins actually belonged together in a single bin. The resulting combined bins underwent assembly procedures to regenerate the consensus sequences.


[0234] The final assembled templates were subsequently annotated using the following procedure. Template sequences were analyzed using BLASTn (v2.0, NCBI) versus gbpri (GenBank version 124). “Hits” were defined as an exact match having from 95% local identity over 200 base pairs through 100% local identity over 100 base pairs, or a homolog match having an E-value, i.e. a probability score, of <1×10−8. The hits were subject to frameshift FASTx versus GENPEPT (GenBank version 124). (See Table 8). In this analysis, a homolog match was defined as having an E-value of <1×10−8. The assembly method used above was described in “System and Methods for Analyzing Biomolecular Sequences,” U.S. Ser. No. 09/276,534, filed Mar. 25, 1999, and the LIFESEQ Gold user manual (Incyte) both incorporated by reference herein.


[0235] Following assembly, template sequences were subjected to motif, BLAST, and functional analyses, and categorized in protein hierarchies using methods described in, e.g., “Database System Employing Protein Function Hierarchies for Viewing Biomolecular Sequence Data,” U.S. Ser. No. 08/812,290, filed Mar. 6, 1997; “Relational Database for Storing Biomolecule Information,” U.S. Ser. No. 08/947,845, filed Oct. 9, 1997; “Project-Based Full-Length Biomolecular Sequence Database,” U.S. Ser. No. 08/811,758, filed Mar. 6, 1997; and “Relational Database and System for Storing Information Relating to Biomolecular Sequences,” U.S. Ser. No. 09/034,807, filed Mar. 4, 1998, all of which are incorporated by reference herein.


[0236] The template sequences were further analyzed by translating each template in all three forward reading frames and searching each translation against the Pfam database of hidden Markov model-based protein families and domains using the HMMER software package (available to the public from Washington University School of Medicine, St. Louis Mo.). Regions of templates which, when translated, contained polarity to Pfam consensus sequences are reported in Table 3, along with descriptions of Pfam protein domains and families. Only those Pfam hits with an E-value of <1×10−3 are reported. (See also World Wide Web site http://pfam.wustl.edu/ for detailed descriptions of Pfam protein domains and families.)


[0237] Additionally, the template sequences were translated in all three forward reading frames, and each translation was searched against hidden Markov models for signal peptides using the HMMER software package. Construction of hidden Markov models and their usage in sequence analysis has been described. (See, for example, Eddy, S. R. (1996) Curr. Opin. Str. Biol. 6:361-365.) Only those signal peptide hits with a cutoff score of 11 bits or greater are reported. A cutoff score of 11 bits or greater corresponds to at least about 91-94% true-positives in signal peptide prediction. Template sequences were also translated in all three forward reading frames, and each translation was searched against TMAP, a program that uses weight matrices to delineate transmembrane segments on protein sequences and determine orientation, with respect to the cell cytosol (Persson, B. and P. Argos (1994) J. Mol. Biol. 237:182-192; Persson, B. and P. Argos (1996) Protein Sci. 5:363-371.) Regions of templates which, when translated, contain similarity to signal peptide or transmembrane consensus sequences are reported in Table 4.


[0238] The results of HMMER analysis as reported in Tables 3 and 4 may support the results of BLAST analysis as reported in Table 2 or may suggest alternative or additional properties of template-encoded polypeptides not previously uncovered by BLAST or other analyses.


[0239] Template sequences are further analyzed using the bioinformatics tools listed in Table 8, or using sequence analysis software known in the art such as MACDNASIS PRO software (Hitachi Software Engineering, South San Francisco Calif.) and LASERGENE software (DNASTAR). Template sequences may be further queried against public databases such as the GenBank rodent, mammalian, vertebrate, prokaryote, and eukaryote databases.


[0240] The template sequences were translated to derive the corresponding longest open reading frame as presented by the polypeptide sequences as reported in Table 2. Alternatively, a polypeptide of the invention may begin at any of the methionine residues within the full length translated polypeptide. Polypeptide sequences were subsequently analyzed by querying against the GenBank protein database (GENPEPT, (GenBank version 124)). Full length polynucleotide sequences are also analyzed using MACDNASIS PRO software (Hitachi Software Engineering, South San Francisco Calif.) and LASERGENE software (DNASTAR). Polynucleotide and polypeptide sequence alignments are generated using default parameters specified by the CLUSTAL algorithm as incorporated into the MEGALIGN multisequence alignment program (DNASTAR), which also calculates the percent identity between aligned sequences.


[0241] Table 7 shows sequences with homology to the polypeptides of the invention as identified by BLAST analysis against a GenBank protein (GENPEPT) database. Column 1 shows the polypeptide sequence identification number (SEQ ID NO:) for the polypeptide segments of the invention. Column 2 shows the reading frame used in the translation of the polynucleotide sequences encoding the polypeptide segments. Column 3 shows the length of the translated polypeptide segments. Columns 4 and 5 show the start and stop nucleotide positions of the polynucleotide sequences encoding the polypeptide segments. Column 6 shows the GenBank identification number (GI Number) of the nearest GenBank homolog. Column 7 shows the probability score for the match between each polypeptide and its GenBank homolog. Column 8 shows the annotation of the GenBank homolog.


[0242] V. Analysis of Polynucleotide Expression


[0243] Northern analysis is a laboratory technique used to detect the presence of a transcript of a gene and involves the hybridization of a labeled nucleotide sequence to a membrane on which RNAs from a particular cell type or tissue have been bound. (See, e.g., Sambrook, supra, ch. 7; Ausubel, 1995, supra, ch. 4 and 16.)


[0244] Analogous computer techniques applying BLAST were used to search for identical or related molecules in cDNA databases such as GenBank or LIFESEQ (Incyte Genomics). This analysis is much faster than multiple membrane-based hybridizations. In addition, the sensitivity of the computer search can be modified to determine whether any particular match is categorized as exact or similar. The basis of the search is the product score, which is defined as:
1BLASTScore×PercentIdentity5×minimum{length(Seq.1),length(Seq.2)}


[0245] The product score takes into account both the degree of similarity between two sequences and the length of the sequence match. The product score is a normalized value between 0 and 100, and is calculated as follows: the BLAST score is multiplied by the percent nucleotide identity and the product is divided by (5 times the length of the shorter of the two sequences). The BLAST score is calculated by assigning a score of +5 for every base that matches in a high-scoring segment pair (HSP), and −4 for every mismatch. Two sequences may share more than one HSP (separated by gaps). If there is more than one HSP, then the pair with the highest BLAST score is used to calculate the product score. The product score represents a balance between fractional overlap and quality in a BLAST alignment. For example, a product score of 100 is produced only for 100% identity over the entire length of the shorter of the two sequences being compared. A product score of 70 is produced either by 100% identity and 70% overlap at one end, or by 88% identity and 100% overlap at the other. A product score is produced either by 100% identity and 50% overlap at one end, or 79% identity and 100% overlap.


[0246] VI. Tissue Distribution Profiling


[0247] A tissue distribution profile is determined for each template by compiling the cDNA library tissue classifications of its component cDNA sequences. Each component sequence, is derived from a cDNA library constructed from a human tissue. Each human tissue is classified into one of the following categories: cardiovascular system; connective tissue; digestive system; embryonic structures; endocrine system; exocrine glands; genitalia, female; genitalia, male; germ cells; hemic and immune system; liver; musculoskeletal system; nervous system; pancreas; respiratory system; sense organs; skin; stomatognathic system; unclassified/mixed; or urinary tract. Template sequences, component sequences, and cDNA library/tissue information are found in the LIFESEQ GOLD database (Incyte Genomics, Palo Alto Calif.).


[0248] Table 6 shows the tissue distribution profile for the templates of the invention. For each template, the three most frequently observed tissue categories are shown in column 3, along with the percentage of component sequences belonging to each category. Only tissue categories with percentage values of ≧10% are shown. A tissue distribution of “widely distributed” in column 3 indicates percentage values of <10% in all tissue categories.


[0249] VII. Transcript Image Analysis


[0250] Transcript images are generated as described in Seilhamer et al., “Comparative Gene Transcript Analysis,” U.S. Pat. No. 5,840,484, incorporated herein by reference.


[0251] VIII. Extension of Polynucleotide Sequences and Isolation of a Full-Length cDNA


[0252] Oligonucleotide primers designed using an mddt of the Sequence Listing are used to extend the nucleic acid sequence. One primer is synthesized to initiate 5′ extension of the template, and the other primer, to initiate 3′ extension of the template. The initial primers may be designed using OLIGO 4.06 software (National Biosciences, Inc. (National Biosciences), Plymouth Minn.), or another appropriate program, to be about 22 to 30 nucleotides in length, to have a GC content of about 50% or more, and to anneal to the target sequence at temperatures of about 68° C. to about 72° C. Any stretch of nucleotides which would result in hairpin structures and primer-primer dimerizations are avoided. Selected human cDNA libraries are used to extend the sequence. If more than one extension is necessary or desired, additional or nested sets of primers are designed.


[0253] High fidelity amplification is obtained by PCR using methods well known in the art. PCR is performed in 96-well plates using the PTC-200 thermal cycler (MJ Research). The reaction mix contains DNA template, nmol of each primer, reaction buffer containing Mg2+, (NH4)2SO4, and β-mercaptoethanol, Taq DNA polymerase (Amersham Pharmacia Biotech), ELONGASE enzyme (Life Technologies), and Pfu DNA polymerase (Stratagene), with the following parameters for primer pair PCI A and PCI B: Step 1: 94° C., 3 min; Step 2: 94° C. 15 sec; Step 3: 60° C., 1 min: Step 4: 68° C. 2 min; Step 5: Steps 2, 3, and 4 repeated 20 times; Step 6: 68° C., 5 min; Step 7: storage at 4° C. In the alternative, the parameters for primer pair T7 and SK+ are as follows: Step 1: 94° C. 3 min; Step 2: 94° C., 15 sec; Step 3: 57° C., 1 min; Step 4: 68° C., 2 min; Step 5: Steps 2, 3, and 4 repeated 20 times; Step 6: 68° C., 5 min; Step 7: storage at 4° C.


[0254] The concentration of DNA in each well is determined by dispensing 100 μl PICOGREEN quantitation reagent (0.25% (v/v); Molecular Probes) dissolved in 1× Tris-EDTA (TE) and 0.5 μl of undiluted PCR product into each well of an opaque fluorimeter plate (Corning Incorporated (Corning), Corning N.Y.), allowing the DNA to bind to the reagent. The plate is scanned in a FLUOROSKAN II (Labsystems Oy) to measure the fluorescence of the sample and to quantify the concentration of DNA. A 5 μl to 10 μl aliquot of the reaction mixture is analyzed by electrophoresis on a 1% agarose mini-gel to determine which reactions are successful in extending the sequence.


[0255] The extended nucleotides are desalted and concentrated, transferred to 384-well plates, digested with CviJI cholera virus endonuclease (Molecular Biology Research, Madison Wis.), and sonicated or sheared prior to religation into pUC 18 vector (Amersham Pharmacia Biotech). For shotgun sequencing, the digested nucleotides are separated on low concentration (0.6 to 0.8%) agarose gels, fragments are excised, and agar digested with AGAR ACE (Promega). Extended clones are religated using T4 ligase (New England Biolabs, Inc., Beverly Mass.) into pUC 18 vector (Amersham Pharmacia Biotech), treated with Pfu DNA polymerase (Stratagene) to fill-in restriction site overhangs, and transfected into competent E. coli cells. Transformed cells are selected on antibiotic-containing media, individual colonies are picked and cultured overnight at 37° C. in 384-well plates in LB/2× carbenicillin liquid media.


[0256] The cells are lysed, and DNA is amplified by PCR using Taq DNA polymerase (Amersham Pharmacia Biotech) and Pfu DNA polymerase (Stratagene) with the following parameters: Step 1: 94° C., 3 min; Step 2: 94° C., 15 sec; Step 3: 60° C., 1 min; Step 4: 72° C., 2 min; Step 5: steps 2, 3, and 4 repeated 29 times; Step 6: 72° C., 5 min; Step 7: storage at 4° C. DNA is quantified by PICOGREEN reagent (Molecular Probes) as described above. Samples with low DNA recoveries are reamplified using the same conditions as described above. Samples are diluted with 20% dimethysulfoxide (1:2, v/v), and sequenced using DYENAMIC energy transfer sequencing primers and the DYENAMIC DIRECT kit (Amersham Pharmacia Biotech) or the ABI PRISM BIGDYE Terminator cycle sequencing ready reaction kit (Applied Biosystems).


[0257] In like manner, the mddt is used to obtain regulatory sequences (promoters, introns, and enhancers) using the procedure above, oligonucleotides designed for su extension, and an appropriate genomic library.


[0258] IX. Labeling of Probes and Southern Hybridization Analyses


[0259] Hybridization probes derived from the mddt of the Sequence Listing are employed for screening cDNAs, mRNAs, or genomic DNA. The labeling of probe nucleotides between 100 and 1000 nucleotides in length is specifically described, but essentially the same procedure may be used with larger cDNA fragments. Probe sequences are labeled at room temperature for 30 minutes using a T4 polynucleotide kinase, γ32P-ATP, and 0.5×One-Phor-AII Plus (Amersham Pharmacia Biotech) buffer and purified using a ProbeQuant G-50 Microcolumn (Amersham Pharmacia Biotech). The probe mixture is diluted to 107 dpm/μg/ml hybridization buffer and used in a typical membrane-based hybridization analysis.


[0260] The DNA is digested with a restriction endonuclease such as Eco RV and is electrophoresed through a 0.7% agarose gel. The DNA fragments are transferred from the agarose to nylon membrane (NYTRAN Plus, Schleicher & Schuell, Inc., Keene N.H.) using procedures specified by the manufacturer of the membrane. Prehybridization is carried out for three or more hours at 68° C., and hybridization is carried out overnight at 68° C. To remove non-specific signals, blots are sequentially washed at room temperature under increasingly stringent conditions, up to 0.1× saline sodium citrate (SSC) and 0.5% sodium dodecyl sulfate. After the blots are placed in a PHOSPHORIMAGER cassette (Molecular Dynamics) or are exposed to autoradiography film, hybridization patterns of standard and experimental lanes are compared. Essentially the same procedure is employed when screening RNA.


[0261] X. Chromosome Mapping of mddt


[0262] The cDNA sequences which were used to assemble SEQ ID NO:1-252 are compared with sequences from the Incyte LIFESEQ database and public domain databases using BLAST and other implementations of the Smith-Waterman algorithm. Sequences from these databases that match SEQ ID NO:1-252 are assembled into clusters of contiguous and overlapping sequences using assembly algorithms such as PHRAP (Table 8). Radiation hybrid and genetic mapping data available from public resources such as the Stanford Human Genome Center (SHGC), Whitehead Institute for Genome Research (WIGR), and Généthon are used to determine if any of the clustered sequences have been previously mapped. Inclusion of a mapped sequence in a cluster will result in the assignment of all sequences of that cluster, including its particular SEQ ID NO:, to that map location. The genetic map locations of SEQ ID NO:1-252 are described as ranges, or intervals, of human chromosomes. The map position of an interval, in centiMorgans, is measured relative to the terminus of the chromosome's p-. The centiMorgan (cM) is a unit of measurement based on recombination frequencies between chromosomal markers. On average, 1 cM is roughly equivalent to 1 megabase (Mb) of DNA in humans, although this can vary widely due to hot and cold spots of recombination.) The cM distances are based on genetic markers mapped by Généthon which provide boundaries for radiation hybrid markers whose sequences were included in each of the clusters.


[0263] XI. Microarray Analysis


[0264] Probe Preparation from Tissue or Cell Samples


[0265] Total RNA is isolated from tissue samples using the guanidinium thiocyanate method and polyA+ RNA is purified using the oligo (dT) cellulose method. Each polyA+ RNA sample is reverse transcribed using MMLV reverse-transcriptase, 0.05 pg/μl oligo-dT primer (21mer), 1× first strand buffer, 0.03 units/μl RNase inhibitor, 500 μM dATP, 500 μM dGTP, 500 μM dTTP, 40 μM dCTP, 40 μM dCTP-Cy3 (BDS) or dCTP-Cy5 (Amersham Pharmacia Biotech). The reverse transcription reaction is performed in a 25 ml volume containing 200 ng polyA+ RNA with GEMBRIGHT kits (Incyte). Specific control polyA+ RNAs are synthesized by in vitro transcription from non-coding yeast genomic DNA (W. Lei, unpublished). As quantitative controls, the control mRNAs at 0.002 ng, 0.02 ng, 0.2 ng, and 2 ng are diluted into reverse transcription reaction at ratios of 1:100,000, 1:10,000, 1:1000, 1:100 (w/w) to sample mRNA respectively. The control mRNAs are diluted into reverse transcription reaction at ratios of 1:3, 3:1, 1:10, 10:1, 1:25, 25:1 (w/w) to sample mRNA differential expression patterns. After incubation at 37° C. for 2 hr, each reaction sample (one with Cy3 and another with Cy5 labeling) is treated with 2.5 ml of 0.5M sodium hydroxide and incubated for 20 minutes at 85° C. to the stop the reaction and degrade the RNA. Probes are purified using two successive CHROMA SPIN 30 gel filtration spin columns (CLONTECH Laboratories, Inc. (CLONTECH), Palo Alto Calif.) and after combining, both reaction samples are ethanol precipitated using 1 ml of glycogen (1 mg/ml), 60 ml sodium acetate, and 300 ml of 100% ethanol. The probe is then dried to completion using a SpeedVAC (Savant Instruments Inc., Holbrook N.Y.) and resuspended in 14 μl 5×SSC/0.2% SDS.


[0266] Microarray Preparation


[0267] Sequences of the present invention are used to generate array elements. Each array element is amplified from bacterial cells containing vectors with cloned cDNA inserts. PCR amplification uses primers complementary to the vector sequences flanking the cDNA insert. Array elements are amplified in thirty cycles of PCR from an initial quantity of 1-2 ng to a final quantity greater than 5 μg. Amplified array elements are then purified using SEPHACRYL-400 (Amersham Pharmacia Biotech).


[0268] Purified array elements are immobilized on polymer-coated glass slides. Glass microscope slides (Corning) are cleaned by ultrasound in 0.1% SDS and acetone, with extensive distilled water washes between and after treatments. Glass slides are etched in 4% hydrofluoric acid (VWR Scientific Products Corporation (VWR), West Chester, Pa.), washed extensively in distilled water, and coated with 0.05% aminopropyl silane (Sigma) in 95% ethanol. Coated slides are cured in a 110° C. oven.


[0269] Array elements are applied to the coated glass substrate using a procedure described in U.S. Pat. No. 5,807,522, incorporated herein by reference. 1 μl of the array element DNA, at an average concentration of 100 ng/μl, is loaded into the open capillary printing element by a high-speed robotic apparatus. The apparatus then deposits about 5 nl of array element sample per slide.


[0270] Microarrays are UV-crosslinked using a STRATALINKER UV-crosslinker (Stratagene). Microarrays are washed at room temperature once in 0.2% SDS and three times in distilled water. Non-specific binding sites are blocked by incubation of microarrays in 0.2% casein in phosphate buffered saline (PBS) (Tropix, Inc., Bedford, Mass.) for 30 minutes at 60° C. followed by washes in 0.2% SDS and distilled water as before.


[0271] Hybridization


[0272] Hybridization reactions contain 9 μl of probe mixture consisting of 0.2 μg each of Cy3 and Cy5 labeled cDNA synthesis products in 5×SSC, 0.2% SDS hybridization buffer. The probe mixture is heated to 65° C. for 5 minutes and is aliquoted onto the microarray surface and covered with an 1.8 cm2 coverslip. The arrays are transferred to a waterproof chamber having a cavity just slightly larger than a microscope slide. The chamber is kept at 100% humidity internally by the addition of 140 μl of 5×SSC in a corner of the chamber. The chamber containing the arrays is incubated for about 6.5 hours at 60° C. The arrays are washed for 10 min at 45° C. in a first wash buffer (1×SSC, 0.1% SDS), three times for 10 minutes each at 45° C. in a second wash buffer (0.1×SSC), and dried.


[0273] Detection


[0274] Reporter-labeled hybridization complexes are detected with a microscope equipped with an Innova 70 mixed gas 10 W laser (Coherent, Inc., Santa Clara Calif.) capable of generating spectral lines at 488 nm for excitation of Cy3 and at 632 nm for excitation of Cy5. The excitation laser light is focused on the array using a 20× microscope objective (Nikon, Inc., Melville N.Y.). The slide containing the array is placed on a computer-controlled X-Y stage on the microscope and raster-scanned past the objective. The 1.8 cm×1.8 cm array used in the present example is scanned with a resolution of 20 micrometers.


[0275] In two separate scans, a mixed gas multiline laser excites the two fluorophores sequentially. Emitted light is split, based on wavelength, into two photomultiplier tube detectors (PMT R1477, Hamamatsu Photonics Systems, Bridgewater N.J.) corresponding to the two fluorophores. Appropriate filters positioned between the array and the photomultiplier tubes are used to filter the signals. The emission maxima of the fluorophores used are 565 nm for Cy3 and 650 nm for Cy5. Each array is typically scanned twice, one scan per fluorophore using the appropriate filters at the laser source, although the apparatus is capable of recording the spectra from both fluorophores simultaneously.


[0276] The sensitivity of the scans is typically calibrated using the signal intensity generated by a cDNA control species added to the probe mix at a known concentration. A specific location on the array contains a complementary DNA sequence, allowing the intensity of the signal at that location to be correlated with a weight ratio of hybridizing species of 1:100,000. When two probes from different sources (e.g., representing test and control cells), each labeled with a different fluorophore, are hybridized to a single array for the purpose of identifying genes that are differentially expressed, the calibration is done by labeling samples of the calibrating cDNA with the two fluorophores and adding identical amounts of each to the hybridization mixture.


[0277] The output of the photomultiplier tube is digitized using a 12-bit RTI-835H analog-to-digital (A/D) conversion board (Analog Devices, Inc., Norwood, Mass.) installed in an IBM-compatible PC computer. The digitized data are displayed as an image where the signal intensity is mapped using a linear 20-color transformation to a pseudocolor scale ranging from blue (low signal) to red (high signal). The data is also analyzed quantitatively. Where two different fluorophores are excited and measured simultaneously, the data are first corrected for optical crosstalk (due to overlapping emission spectra) between the fluorophores using each fluorophore's emission spectrum.


[0278] A grid is superimposed over the fluorescence signal image such that the signal from each spot is centered in each element of the grid. The fluorescence signal within each element is then integrated to obtain a numerical value corresponding to the average intensity of the signal. The software used for signal analysis is the GEMTOOLS gene expression analysis program (Incyte).


[0279] XII. Complementary Nucleic Acids


[0280] Sequences complementary to the mddt are used to detect, decrease, or inhibit expression of the naturally occurring nucleotide. The use of oligonucleotides comprising from about 15 to 30 base pairs is typical in the art. However, smaller or larger sequence fragments can also be used. Appropriate oligonucleotides are designed from the mddt using OLIGO 4.06 software (National Biosciences) or other appropriate programs and are synthesized using methods standard in the art or ordered from a commercial supplier. To inhibit transcription, a complementary oligonucleotide is designed from the most unique 5′ sequence and used to prevent transcription factor binding to the promoter sequence. To inhibit translation, a complementary oligonucleotide is designed to prevent ribosomal binding and processing of the transcript.


[0281] XIII. Expression of MDDT


[0282] Expression and purification of MDDT is accomplished using bacterial or virus-based expression systems. For expression of MDDT in bacteria, cDNA is subcloned into an appropriate vector containing an antibiotic resistance gene and an inducible promoter that directs high levels of cDNA transcription. Examples of such promoters include, but are not limited to, the trp-lac (tac) hybrid promoter and the T5 or T7 bacteriophage promoter in conjunction with the lac operator regulatory element. Recombinant vectors are transformed into suitable bacterial hosts. e.g., BL21(DE3). Antibiotic resistant bacteria express MDDT upon induction with isopropyl beta-D-thiogalactopyranoside (IPTG). Expression of MDDT in eukaryotic cells is achieved by infecting insect or mammalian cell lines with recombinant Autographica californica nuclear polyhedrosis virus (AcMNPV), commonly known as baculovirus. The nonessential polyhedrin gene of baculovirus is replaced with cDNA encoding MDDT by either homologous recombination or bacterial-mediated transposition involving transfer plasmid intermediates. Viral infectivity is maintained and the strong polyhedrin promoter drives high levels of cDNA transcription. Recombinant baculovirus is used to infect Spodoptera frugiperda (Sf9) insect cells in most cases, or human hepatocytes, in some cases. Infection of the latter requires additional genetic modifications to baculovirus. (See e.g., Engelhard, supra, and Sandig, supra.)


[0283] In most expression systems, MDDT is synthesized as a fusion protein with, e.g., glutathione S-transferase (GST) or a peptide epitope tag, such as FLAG or 6-His, permitting rapid, single-step, affinity-based purification of recombinant fusion protein from crude cell lysates. GST, a 26-kilodalton enzyme from Schistosoma japonicum, enables the purification of fusion proteins on immobilized glutathione under conditions that maintain protein activity and antigenicity (Amersham Pharmacia Biotech). Following purification, the GST moiety can be proteolytically cleaved from MDDT at specifically engineered sites. FLAG, an 8-amino acid peptide, enables immunoaffinity purification using commercially available monoclonal and polyclonal anti-FLAG antibodies (Eastman Kodak Company, Rochester N.Y.). 6-His, a stretch of six consecutive histidine residues, enables purification on metal-chelate resins (QIAGEN). Methods for protein expression and purification are discussed in Ausubel (1995, supra, Chapters 10 and 16). Purified MDDT obtained by these methods can be used directly in the following activity assay.


[0284] XIV. Demonstration of MDDT Activity


[0285] MDDT, or biologically active fragments thereof, are labeled with 251I Bolton-Hunter reagent. (See, e.g., Bolton, A. E. and W. M. Hunter (1973) Biochem. J. 133:529-539.) Candidate molecules previously arrayed in the wells of a multi-well plate are incubated with the labeled MDDT, washed, and any wells with labeled MDDT complex are assayed. Data obtained using different concentrations of MDDT are used to calculate values for the number, affinity, and association of MDDT with the candidate molecules.


[0286] Alternatively, molecules interacting with MDDT are analyzed using the yeast two-hybrid system as described in Fields, S. and O. Song (1989) Nature 340:245-246, or using commercially available kits based on the two-hybrid system, such as the MATCHMAKER system (CLONTECH).


[0287] MDDT may also be used in the PATHCALLING process (CuraGen Corp. New Haven Conn.) which employs the yeast two-hybrid system in a high-throughput manner to determine all interactions between the proteins encoded by two large libraries of genes (Nandabalan, K. et al. (2000) U.S. Pat. No. 6,057,101).


[0288] XV. Functional Assays


[0289] MDDT function is assessed by expressing mddt at physiologically elevated levels in mammalian cell culture systems. cDNA is subcloned into a mammalian expression vector containing a strong promoter that drives high levels of cDNA expression. Vectors of choice include pCMV SPORT (Life Technologies) and pCR3.1 (Invitrogen Corporation, Carlsbad Calif.), both of which contain the cytomegalovirus promoter. 5-10 μg of recombinant vector are transiently transfected into a human cell line, preferably of endothelial or hematopoietic origin, using either liposome formulations or electroporation. 1-2 μg of an additional plasmid containing sequences encoding a marker protein are co-transfected.


[0290] Expression of a marker protein provides a means to distinguish transfected cells from nontransfected cells and is a reliable predictor of cDNA expression from the recombinant vector. Marker proteins of choice include, e.g., Green Fluorescent Protein (GFP; CLONTECH), CD64, or a CD64-GFP fusion protein. Flow cytometry (FCM), an automated laser optics-based technique, is used to identify transfected cells expressing GFP or CD64-GFP and to evaluate the apoptotic state of the cells and other cellular properties.


[0291] FCM detects and quantifies the uptake of fluorescent molecules that diagnose events preceding or coincident with cell death. These events include changes in nuclear DNA content as measured by staining of DNA with propidium iodide; changes in cell size and granularity as measured by forward light scatter and 90 degree side light scatter; down-regulation of DNA synthesis as measured by decrease in bromodeoxyuridine uptake; alterations in expression of cell surface and intracellular proteins as measured by reactivity with specific antibodies; and alterations in plasma membrane composition as measured by the binding of fluorescein-conjugated Annexin V protein to the cell surface. Methods in flow cytometry are discussed in Ormerod, M. G. (1994) Flow Cytometry, Oxford, New York N.Y.


[0292] The influence of MDDT on gene expression can be assessed using highly purified populations of cells transfected with sequences encoding MDDT and either CD64 or CD64-GFP. CD64 and CD64-GFP are expressed as the surface of transfected cells and bind to observed regions of human immunoglobulin G (IgG). Transfected cells are efficiently separated from nontransfected cells using magnetic beads coated with either human IgG or antibody against CD64 (DYNAL, Inc., Lake Success N.Y.). mRNA can be purified from the cells using methods well known by those of skill in the art. Expression of mRNA encoding MDDT and other genes of interest can be analyzed by northern analysis or microarray techniques.


[0293] XVI. Production of Antibodies


[0294] MDDT substantially purified using polyacrylamide gel electrophoresis (PAGE; see, e.g., Harrington, M. G. (1990) Methods Enzymol. 182:488-495), or other purification techniques, is used to immunize rabbits and to produce antibodies using standard protocols.


[0295] Alternatively, the MDDT amino acid sequence is analyzed using LASERGENE software (DNASTAR) to determine regions of high immunogenicity, and a corresponding peptide is synthesized and used to raise antibodies by means known to those of skill in the art. Methods for selection of appropriate epitopes, such as those near the C-terminus or in hydrophilic regions are well described in the art. (See, e.g., Ausubel, 1995, supra, Chapter 11.)


[0296] Typically, peptides 15 residues in length are synthesized using an ABI 431A peptide synthesizer (Applied Biosystems) using fmoc-chemistry and coupled to KLH (Sigma) by reaction with N-maleimidobenzoyl-N-hydroxysuccinimide ester (MBS) to increase immunogenicity. (See, e.g., Ausubel, supra.) Rabbits are immunized with the peptide-KLH complex in complete Freund's adjuvant. Resulting antisera are tested for antipeptide activity by, for example, binding the peptide to plastic, blocking with 1% BSA, reacting with rabbit antisera, washing, and reacting with radio-iodinated goat anti-rabbit IgG. Antisera with antipeptide activity are tested for anti-MDDT activity using protocols well known in the art, including ELISA, RIA, and immunoblotting.


[0297] XVII. Purification of Naturally Occurring MDDT Using Specific Antibodies


[0298] Naturally occurring or recombinant MDDT is substantially purified by immunoaffinity chromatography using antibodies specific for MDDT. An immunoaffinity column is constructed by covalently coupling anti-MDDT antibody to an activated chromatographic resin, such as CNBr-activated SEPHAROSE (Amersham Pharmacia Biotech). After the coupling, the resin is blocked and washed according to the manufacturer's instructions.


[0299] Media containing MDDT are passed over the immunoaffinity column, and the column is washed under conditions that allow the preferential absorbance of MDDT (e.g., high ionic strength buffers in the presence of detergent). The column is eluted under conditions that disrupt antibody/MDDT binding (e.g., a buffer of pH 2 to pH 3, or a high concentration of a chaotrope, such as urea or thiocyanate iond MDDT is collected.


[0300] All publications and patents mentioned in the above specification are herein incorporated by reference. Various modifications and variations of the described method and system of the invention will be apparent to those skilled in the art without departing from the scope and spirit of the invention. Although the invention has been described in connection with specific preferred embodiments, it should be understood that the invention as claimed should not be unduly limited to such specific embodiments. Indeed, various modifications of the above-described modes for carrying out the invention which are obvious to those skilled in the field of molecular biology or related fields are intended to be within the scope of the following claims.
2TABLE 1SEQ ID NO:Template IDSEQ ID NO:ORF ID1LG:150318.1:2000SEP08253LG:150318.1.orf2:2000SEP082LG:022529.1:2000SEP08254LG:022529.1.orf1:2000SEP083LG:352559.1:2000SEP08255LG:352559.1.orf2:2000SEP084LG:175223.1:2000SEP08256LG:175223.1.orf3:2000SEP085LG:476989.1:2000SEP08257LG:476989.1.orf2:2000SEP086LG:253268.7:2000SEP08258LG:253268.7.orf1:2000SEP087LG:401322.1:2000SEP08259LG:401322.1.orf1:2000SEP088LG:1328436.1:2000SEP08260LG:1328436.1.orf2:2000SEP089LG:475404.1:2000SEP08261LG:475404.1.orf2:2000SEP0810LG:1384132.1:2000SEP08262LG:1384132.1.orf1:2000SEP0811LG:410804.18:2000SEP08263LG:410804.18.orf1:2000SEP0812LG:1082306.1:2000SEP08264LG:1082306.1.orf1:2000SEP0813LG:233814.4:2000SEP08265LG:233814.4.orf1:2000SEP0814LG:977478.5:2000SEP08266LG:977478.5.orf3:2000SEP0815LG:025931.1:2000SEP08267LG:025931.1.orf2:2000SEP0816LG:885368.1:2000SEP08268LG:885368.1.orf1:2000SEP0817LG:1054900.1:2000SEP08269LG:1054900.1.orf3:2000SEP0818LG:995186.2:2000SEP08270LG:995186.2.orf3:2000SEP0819LG:435048.23:2000SEP08271LG:435048.23.orf2:2000SEP0820LG:954859.1:2000SEP08272LG:954859.1.orf2:2000SEP0821LG:364370.1:2000SEP08273LG:364370.1.orf3:2000SEP0822LG:1098789.1:2000SEP08274LG:1098789.1.orf3:2000SEP0823LG:201540.2:2000SEP08275LG:201540.2.orf2:2000SEP0824LG:1077357.1:2000SEP08276LG:1077357.1.orf1:2000SEP0825LG:1048846.4:2000SEP08277LG:1048846.4.orf3:2000SEP0826LG:336685.1:2000SEP08278LG:336685.1.orf3:2000SEP0827LG:1076253.1:2000SEP08279LG:1076253.1.orf3:2000SEP0828LG:1400601.2:2000SEP08280LG:1400601.2.orf3:2000SEP0829LG:1079092.3:2000SEP08281LG:1079092.3.orf2:2000SEP0830LG:1086064.1:2000SEP08282LG:1086064.1.orf2:2000SEP0831LG:1400608.1:2000SEP08283LG:1400608.1.orf3:2000SEP0832LG:399275.5:2000SEP08284LG:399275.5.orf1:2000SEP0833LG:293943.1:2000SEP08285LG:293943.1.orf1:2000SEP0834LG:345884.1:2000SEP08286LG:345884.1.orf2:2000SEP0835LG:400967.1:2000SEP08287LG:400967.1.orf1:2000SEP0836LG:024556.6:2000SEP08288LG:024556.6.orf1:2000SEP0837LG:081189.3:2000SEP08289LG:081189.3.orf2:2000SEP0838LG:018258.1:2000SEP08290LG:018258.1.orf3:2000SEP0839LG:450399.3:2000SEP08291LG:450399.3.orf3:2000SEP0840LG:451122.1:2000SEP08292LG:451122.1.orf1:2000SEP0841LG:451682.1:2000SEP08293LG:451682.1.orf3:2000SEP0842LG:238631.4:2000SEP08294LG:238631.4.orf3:2000SEP0843LG:236654.1:2000SEP08295LG:236654.1.orf3:2000SEP0844LG:332655.1:2000SEP08296LG:332655.1.orf1:2000SEP0845LG:217396.2:2000SEP08297LG:217396.2.orf1:2000SEP0846LG:090574.1:2000SEP08298LG:090574.1.orf3:2000SEP0847LG:202943.1:2000SEP08299LG:202943.1.orf1:2000SEP0848LG:236928.1:2000SEP08300LG:236928.1.orf1:2000SEP0849LG:215169.2:2000SEP08301LG:215169.2.orf2:2000SEP0850LG:410726.1:2000SEP08302LG:410726.1.orf1:2000SEP0851LG:234372.2:2000SEP08303LG:234372.2.orf2:2000SEP0852LG:022629.1:2000SEP08304LG:022629.1.orf3:2000SEP0853LG:068682.1:2000SEP08305LG:068682.1.orf2:2000SEP0854LG:222335.1:2000SEP08306LG:222335.1.orf1:2000SEP0855LG:331342.1:2000SEP08307LG:331342.1.orf3:2000SEP0856LG:021770.1:2000SEP08308LG:021770.1.orf3:2000SEP0857LG:181607.9:2000SEP08309LG:181607.9.orf2:2000SEP0858LG:1042768.1:2000SEP08310LG:1042768.1.orf3:2000SEP0859LG:282729.1:2000SEP08311LG:282729.1.orf1:2000SEP0860LG:998305.3:2000SEP08312LG:998305.3.orf2:2000SEP0861LG:1135213.1:2000SEP08313LG:1135213.1.orf1:2000SEP0862LG:267762.1:2000SEP08314LG:267762.1.orf1:2000SEP0863LG:120744.1:2000SEP08315LG:120744.1.orf1:2000SEP0864LG:403409.1:2000SEP08316LG:403409.1.orf3:2000SEP0865LG:226874.3:2000SEP08317LG:226874.3.orf1:2000SEP0866LG:1045521.4:2000SEP08318LG:1045521.4.orf1:2000SEP0867LG:275876.1:2000SEP08319LG:275876.1.orf1:2000SEP0868LG:475127.7:2000SEP08320LG:475127.7.orf1:2000SEP0869LG:157263.1:2000SEP08321LG:157263.1.orf1:2000SEP0870LG:247382.7:2000SEP08322LG:247382.7.orf1:2000SEP0871LG:197367.5:2000SEP08323LG:197367.5.orf2:2000SEP0872LG:218090.5:2000SEP08324LG:218090.5.orf2:2000SEP0873LG:216612.4:2000SEP08325LG:216612.4.orf3:2000SEP0874LG:197614.1:2000SEP08326LG:197614.1.orf1:2000SEP0875LG:378428.1:2000SEP08327LG:378428.1.orf3:2000SEP0876LG:286639.1:2000SEP08328LG:286639.1.orf3:2000SEP0877LG:389870.1:2000SEP08329LG:389870.1.orf1:2000SEP0878LG:1387485.6:2000SEP08330LG:1387485.6.orf2:2000SEP0879LG:230151.1:2000SEP08331LG:230151.1.orf1:2000SEP0880LG:215158.5:2000SEP08332LG:215158.5.orf1:2000SEP0881LG:235840.1:2000SEP08333LG:235840.1.orf2:2000SEP0882LG:350272.1:2000SEP08334LG:350272.1.orf2:2000SEP0883LG:232190.1:2000SEP08335LG:232190.1.orf2:2000SEP0884LG:1068127.1:2000SEP08336LG:1068127.1.orf2:2000SEP0885LG:408751.3:2000SEP08337LG:408751.3.orf2:2000SEP0886LG:1078933.1:2000SEP08338LG:1078933.1.orf1:2000SEP0887LG:958731.1:2000SEP08339LG:958731.1.orf3:2000SEP0888LG:024125.5:2000SEP08340LG:024125.5.orf3:2000SEP0889LG:373637.3:2000SEP08341LG:373637.3.orf1:2000SEP0890LG:1053229.1:2000SEP08342LG:1053229.1.orf1:2000SEP0891LG:248364.1:2000SEP08343LG:248364.1.orf2:2000SEP0892LG:477130.1:2000SEP08344LG:477130.1.orf3:2000SEP0893LG:113786.17:2000SEP08345LG:113786.17.orf2:2000SEP0894LG:347635.1:2000SEP08346LG:347635.1.orf3:2000SEP0895LG:242966.4:2000SEP08347LG:242966.4.orf1:2000SEP0896LG:217814.1:2000SEP08348LG:217814.1.orf3:2000SEP0897LG:476452.1:2000SEP08349LG:476452.1.orf3:2000SEP0898LG:1100657.1:2000SEP08350LG:1100657.1.orf1:2000SEP0899LG:1132418.2:2000SEP08351LG:1132418.2.orf1:2000SEP08100LG:1098570.1:2000SEP08352LG:1098570.1.orf3:2000SEP08101LG:1097987.1:2000SEP08353LG:1097987.1.orf3:2000SEP08102LG:337818.2:2000SEP08354LG:337818.2.orf1:2000SEP08103LG:1040582.1:2000SEP08355LG:1040582.1.orf2:2000SEP08104LG:1099122.1:2000SEP08356LG:1099122.1.orf3:2000SEP08105LG:1327449.1:2000SEP08357LG:1327449.1.orf3:2000SEP08106LG:227933.5:2000SEP08358LG:227933.5.orf1:2000SEP08107LG:1043709.2:2000SEP08359LG:1043709.2.orf3:2000SEP08108LG:1099871.1:2000SEP08360LG:1099871.1.orf1:2000SEP08109LG:1399139.4:2000SEP08361LG:1399139.4.orf3:2000SEP08110LG:236386.1:2000SEP08362LG:236386.1.orf3:2000SEP08111LG:1015157.1:2000SEP08363LG:1015157.1.orf1:2000SEP08112LG:1065433.1:2000SEP08364LG:1065433.1.orf3:2000SEP08113LG:236992.4:2000SEP08365LG:236992.4.orf1:2000SEP08114LG:1071124.1:2000SEP08366LG:1071124.1.orf1:2000SEP08115LG:206425.2:2000SEP08367LG:206425.2.orf2:2000SEP08116LG:885747.2:2000SEP08368LG:885747.2.orf3:2000SEP08117LG:1140501.1:2000SEP08369LG:1140501.1.orf1:2000SEP08118LG:001239.1:2000SEP08370LG:001239.1.orf3:2000SEP08119LG:018980.1:2000SEP08371LG:018980.1.orf1:2000SEP08120LG:1083120.3:2000SEP08372LG:1083120.3.orf3:2000SEP08121LG:233258.3:2000SEP08373LG:233258.3.orf3:2000SEP08122LG:999062.1:2000SEP08374LG:999062.1.orf3:2000SEP08123LG:887776.1:2000SEP08375LG:887776.1.orf3:2000SEP08124LG:1400301.2:2000SEP08376LG:1400301.2.orf1:2000SEP08125LG:1329362.1:2000SEP08377LG:1329362.1.orf2:2000SEP08126LG:1096498.1:2000SEP08378LG:1096498.1.orf2:2000SEP08127LG:1096337.1:2000SEP08379LG:1096337.1.orf2:2000SEP08128LG:1400579.1:2000SEP08380LG:1400579.1.orf2:2000SEP08129LG:1080091.1:2000SEP08381LG:1080091.1.orf2:2000SEP08129LG:1080091.1:2000SEP08382LG:1080091.1.orf3:2000SEP08130LG:1082203.1:2000SEP08383LG:1082203.1.orf1:2000SEP08131LG:1084051.1:2000SEP08384LG:1084051.1.orf3:2000SEP08132LG:1082393.1:2000SEP08385LG:1082393.1.orf3:2000SEP08133LG:1086183.1:2000SEP08386LG:1086183.1.orf2:2000SEP08134LG:1090268.1:2000SEP08387LG:1090268.1.orf3:2000SEP08135LG:1400597.5:2000SEP08388LG:1400597.5.orf1:2000SEP08136LG:1080307.2:2000SEP08389LG:1080307.2.orf3:2000SEP08137LG:1400603.2:2000SEP08390LG:1400603.2.orf2:2000SEP08138LG:1052984.1:2000SEP08391LG:1052984.1.orf1:2000SEP08139LG:1091259.1:2000SEP08392LG:1091259.1.orf3:2000SEP08140LG:1082263.2:2000SEP08393LG:1082263.2.orf3:2000SEP08141LG:1048604.2:2000SEP08394LG:1048604.2.orf3:2000SEP08142LG:1085254.3:2000SEP08395LG:1085254.3.orf2:2000SEP08143LG:1400606.2:2000SEP08396LG:1400606.2.orf1:2000SEP08144LG:1090358.2:2000SEP08397LG:1090358.2.orf1:2000SEP08145LG:1079064.2:2000SEP08398LG:1079064.2.orf1:2000SEP08146LG:1076866.1:2000SEP08399LG:1076866.1.orf2:2000SEP08147LG:969359.1:2000SEP08400LG:969359.1.orf2:2000SEP08148LG:366783.1:2000SEP08401LG:366783.1.orf1:2000SEP08149LG:332176.3:2000SEP08402LG:332176.3.orf2:2000SEP08150LG:994938.1:2000SEP08403LG:994938.1.orf3:2000SEP08151LG:982800.1:2000SEP08404LG:982800.1.orf1:2000SEP08152LG:977850.7:2000SEP08405LG:977850.7.orf1:2000SEP08153LG:234748.2:2000SEP08406LG:234748.2.orf3:2000SEP08154LG:306284.1:2000SEP08407LG:306284.1.orf2:2000SEP08155LI:333170.3:2000SEP08408LI:333170.3.orf1:2000SEP08156LI:336685.2:2000SEP08409LI:336685.2.orf3:2000SEP08157LI:279013.5:2000SEP08410LI:279013.5.orf3:2000SEP08158LI:1037075.1:2000SEP08411LI:1037075.1.orf1:2000SEP08159LI:1073403.1:2000SEP08412LI:1073403.1.orf2:2000SEP08160LI:1075296.1:2000SEP08413LI:1075296.1.orf1:2000SEP08161LI:1085501.1:2000SEP08414LI:1085501.1.orf3:2000SEP08162LI:1086181.1:2000SEP08415LI:1086181.1.orf2:2000SEP08163LI:1164493.1:2000SEP08416LI:1164493.1.orf1:2000SEP08164LI:1175097.1:2000SEP08417LI:1175097.1.orf1:2000SEP08165LI:1092948.1:2000SEP08418LI:1092948.1.orf2:2000SEP08166LI:380378.2:2000SEP08419LI:380378.2.orf3:2000SEP08167LI:1029674.1:2000SEP08420LI:1029674.1.orf3:2000SEP08168LI:2048601.3:2000SEP08421LI:2048601.3.orf2:2000SEP08169LI:1186208.1:2000SEP08422LI:1186208.1.orf2:2000SEP08170LI:1170753.1:2000SEP08423LI:1170753.1.orf1:2000SEP08171LI:1180908.1:2000SEP08424LI:1180908.1.orf2:2000SEP08172LI:1182900.2:2000SEP08425LI:1182900.2.orf1:2000SEP08173LI:1169548.2:2000SEP08426LI:1169548.2.orf3:2000SEP08174LI:1039974.1:2000SEP08427LI:1039974.1.orf1:2000SEP08175LI:1175765.2:2000SEP08428LI:1175765.2.orf3:2000SEP08176LI:313948.1:2000SEP08429LI:313948.1.orf3:2000SEP08177LI:335923.2:2000SEP08430LI:335923.2.orf2:2000SEP08178LI:345884.1:2000SEP08431LI:345884.1.orf1:2000SEP08179LI:417127.1:2000SEP08432LI:417127.1.orf1:2000SEP08180LI:451710.1:2000SEP08433LI:451710.1.orf1:2000SEP08181LI:406882.2:2000SEP08434LI:406882.2.orf1:2000SEP08182LI:728223.1:2000SEP08435LI:728223.1.orf2:2000SEP08183LI:289783.19:2000SEP08436LI:289783.19.orf2:2000SEP08184LI:235255.8:2000SEP08437LI:235255.8.orf2:2000SEP08185LI:237693.5:2000SEP08438LI:237693.5.orf3:2000SEP08186LI:433670.3:2000SEP08439LI:433670.3.orf2:2000SEP08187LI:202943.4:2000SEP08440LI:202943.4.orf2:2000SEP08188LI:068682.1:2000SEP08441LI:068682.1.orf1:2000SEP08189LI:203301.3:2000SEP08442LI:203301.3.orf2:2000SEP08190LI:020726.3:2000SEP08443LI:020726.3.orf2:2000SEP08191LI:027209.1:2000SEP08444LI:027209.1.orf1:2000SEP08192LI:108819.1:2000SEP08445LI:108819.1.orf1:2000SEP08193LI:021759.1:2000SEP08446LI:021759.1.orf2:2000SEP08194LI:1165967.1:2000SEP08447LI:1165967.1.orf1:2000SEP08195LI:1166315.1:2000SEP08448LI:1166315.1.orf3:2000SEP08196LI:204626.1:2000SEP08449LI:204626.1.orf1:2000SEP08197LI:801140.1:2000SEP08450LI:801140.1.orf1:2000SEP08198LI:286639.1:2000SEP08451LI:286639.1.orf1:2000SEP08199LI:288905.4:2000SEP08452LI:288905.4.orf3:2000SEP08200LI:332161.1:2000SEP08453LI:332161.1.orf3:2000SEP08201LI:184867.1:2000SEP08454LI:184867.1.orf1:2000SEP08202LI:229932.4:2000SEP08455LI:229932.4.orf1:2000SEP08203LI:1189932.1:2000SEP08456LI:1189932.1.orf1:2000SEP08204LI:1076689.1:2000SEP08457LI:1076689.1.orf1:2000SEP08205LI:415181.2:2000SEP08458LI:415181.2.orf1:2000SEP08206LI:296358.1:2000SEP08459LI:296358.1.orf3:2000SEP08207LI:205186.3:2000SEP08460LI:205186.3.orf2:2000SEP08208LI:220537.2:2000SEP08461LI:220537.2.orf3:2000SEP08209LI:248364.2:2000SEP08462LI:248364.2.orf2:2000SEP08210LI:2048338.1:2000SEP08463LI:2048338.1.orf3:2000SEP08211LI:1185203.8:2000SEP08464LI:1185203.8.orf3:2000SEP08212LI:021770.3:2000SEP08465LI:021770.3.orf2:2000SEP08213LI:1185841.1:2000SEP08466LI:1185841.1.orf2:2000SEP08214LI:1181710.1:2000SEP08467LI:1181710.1.orf1:2000SEP08215LI:2048959.1:2000SEP08468LI:2048959.1.orf3:2000SEP08216LI:798494.1:2000SEP08469LI:798494.1.orf3:2000SEP08217LI:2049223.1:2000SEP08470LI:2049223.1.orf1:2000SEP08218LI:1177833.1:2000SEP08471LI:1177833.1.orf3:2000SEP08219LI:2049267.1:2000SEP08472LI:2049267.1.orf3:2000SEP08220LI:1165939.1:2000SEP08473LI:1165939.1.orf1:2000SEP08221LI:1170958.1:2000SEP08474LI:1170958.1.orf1:2000SEP08222LI:1089827.1:2000SEP08475LI:1089827.1.orf2:2000SEP08223LI:792112.1:2000SEP08476LI:792112.1.orf2:2000SEP08224LI:282219.2:2000SEP08477LI:282219.2.orf3:2000SEP08225LI:1088010.2:2000SEP08478LI:1088010.2.orf3:2000SEP08226LI:1165276.1:2000SEP08479LI:1165276.1.orf3:2000SEP08227LI:1169524.2:2000SEP08480LI:1169524.2.orf1:2000SEP08228LI:1180255.1:2000SEP08481LI:1180255.1.orf1:2000SEP08229LI:1091903.1:2000SEP08482LI:1091903.1.orf2:2000SEP08230LI:1169219.1:2000SEP08483LI:1169219.1.orf1:2000SEP08231LI:2050313.1:2000SEP08484LI:2050313.1.orf2:2000SEP08232LI:209351.3:2000SEP08485LI:209351.3.orf2:2000SEP08232LI:209351.3:2000SEP08486LI:209351.3.orf3:2000SEP08233LI:119900.1:2000SEP08487LI:119900.1.orf2:2000SEP08234LI:2052274.1:2000SEP08488LI:2052274.1.orf1:2000SEP08235LI:1075502.1:2000SEP08489LI:1075502.1.orf2:2000SEP08236LI:813697.1:2000SEP08490LI:813697.1.orf3:2000SEP08237LI:814261.1:2000SEP08491LI:814261.1.orf3:2000SEP08238LI:775334.1:2000SEP08492LI:775334.1.orf1:2000SEP08239LI:1180325.1:2000SEP08493LI:1180325.1.orf3:2000SEP08240LI:1183147.3:2000SEP08494LI:1183147.3.orf2:2000SEP08241LI:1175373.3:2000SEP08495LI:1175373.3.orf2:2000SEP08242LI:813757.1:2000SEP08496LI:813757.1.orf1:2000SEP08243LI:1182979.2:2000SEP08497LI:1182979.2.orf3:2000SEP08244LI:1177823.2:2000SEP08498LI:1177823.2.orf2:2000SEP08245LI:1174279.1:2000SEP08499LI:1174279.1.orf3:2000SEP08246LI:1178411.1:2000SEP08500LI:1178411.1.orf1:2000SEP08247LI:1182739.1:2000SEP08501LI:1182739.1.orf3:2000SEP08248LI:234937.4:2000SEP08502LI:234937.4.orf1:2000SEP08249LI:1170660.1:2000SEP08503LI:1170660.1.orf2:2000SEP08250LI:1144409.1:2000SEP08504LI:1144409.1.orf1:2000SEP08251LI:246290.10:2000SEP08505LI:246290.10.orf1:2000SEP08252LI:280034.1:2000SEP08506LI:280034.1.orf2:2000SEP08


[0301]

3









TABLE 2








SEQ ID NO:
Template ID
GI Number
Probability Score
Annotation



















1
LG:150318.1:2000SEP08
g11643581
0


Homo sapiens
PR-







domain containing






protein 14






(PRDM14) mRNA,


2
LG:022529.1:2000SEP08
g10047272
0


Homo sapiens








mRNA for KIAA1599






protein, partial cds.


3
LG:352559.1:2000SEP08
g13560887
1.00E−11


Homo sapiens
EZFIT-







related protein 1






mRNA, complete


4
LG:175223.1:2000SEP08
g10433955
1.00E−43
(fl)(Homo sapiens)






unnamed protein


5
LG:476989.1:2000SEP08
g12407394
0


Homo sapiens








tripartite motif






protein TRIM7






(TRIM7) mRNA,


6
LG:253268.7:2000SEP08
g12239368
0


Homo sapiens
LYST-







interacting protein






LIP9 mRNA, partial


7
LG:401322.1:2000SEP08
g13623682
5.00E−26


Homo sapiens
,







tubulin alpha 1,






clone MGC: 2321,


8
LG:1328436.1:2000SEP08
g4589587
2.00E−55


Homo sapiens








mRNA for KIAA0972






protein, complete


9
LG:475404.1:2000SEP08
g10434194
0


Homo sapiens








cDNA FLJ12606 fis,






clone






NT2RM4001483,






moderately similar


10
LG:1384132.1:2000SEP08
g14042849
1.00E−71


Homo sapiens








cDNA FLJ14959 fis,






clone






PLACE4000156,






moderately similar


11
LG:410804.18:2000SEP08
g13543325
3.00E−74


Homo sapiens
,







hypothetical






protein MGC8407,






clone MGC: 1820,






mRNA, complete


12
LG:1082306.1:2000SEP08
g13325336
0


Homo sapiens
,







clone MGC: 10520,






mRNA, complete


13
LG:233814.4:2000SEP08
g10434873
1.00E−166


Homo sapiens








cDNA FLJ13044 fis,






clone






NT2RP3001355,






weakly similar to






TRICARBOXYLATE






TRANSPORT


14
LG:977478.5:2000SEP08
g12698000
0


Homo sapiens








mRNA for KIAA1728






protein, partial cds.


15
LG:025931.1:2000SEP08
g10436359
0


Homo sapiens








cDNA FLJ14011 fis,






clone






Y79AA1002472,






weakly similar to


16
LG:885368.1:2000SEP08
g440824
9.00E−60
(fl)(Arabidopsis








thaliana
) ribosomal



17
LG:1054900.1:2000SEP08
g12052982
0


Homo sapiens








mRNA; cDNA






DKFZp434l1610






(from clone






DKFZp434l1610);


18
LG:995186.2:2000SEP08
g12052982
0


Homo sapiens








mRNA; cDNA






DKFZp434l1610






(from clone






DKFZp434l1610);


19
LG:435048.23:2000SEP08
g10432866
1.00E−177


Homo sapiens








cDNA FLJ11583 fis,






clone






HEMBA1003680,






weakly similar to






PUTATIVE






AMINOPEPTIDASE






ZK353.6 IN


20
LG:954859.1:2000SEP08
g10438224
1.00E−176


Homo sapiens








cDNA: FLJ21990 fis,






clone HEP06386.


21
LG:364370.1:2000SEP08
g14043150
1.00E−163


Homo sapiens
,







ribosomal protein






L13, clone






MGC: 15490, mRNA,


22
LG:1098789.1:2000SEP08
g14029703
1.00E−137


Homo sapiens








myosin regulatory






light chain 2






(MRLC2) mRNA,


23
LG:201540.2:2000SEP08
g12407386
0


Homo sapiens








tripartite motif






protein TRIM5






isoform delta






(TRIM5) mRNA,


24
LG:1077357.1:2000SEP08
g10436361
4.00E−66


Homo sapiens








cDNA FLJ14012 fis,






clone






Y79AA1002482,






moderately similar


25
LG:1048846.4:2000SEP08
g10439974
1.00E−154


Homo sapiens








cDNA: FLJ23327 fis,






clone HEP12630,






highly similar to






HSZNF37 Homo






sapiens ZNF37A


26
LG:336685.1:2000SEP08
g12697317
0


Homo sapiens








partial mRNA for


27
LG:1076253.1:2000SEP08
g7959276
5.00E−34


Homo sapiens








mRNA for KIAA1508






protein, partial cds.


28
LG:1400601.2:2000SEP08
g14042292
0


Homo sapiens








cDNA FLJ14636 fis,






clone






NT2RP2001233,






weakly similar to


29
LG:1079092.3:2000SEP08
g12052982
6.00E−07


Homo sapiens








mRNA; cDNA






DKFZp434l1610






(from clone






DKFZp434l1610);


30
LG:1086064.1:2000SEP08
g10436361
3.00E−76


Homo sapiens








cDNA FLJ14012 fis,






clone






Y79AA1002482,






moderately similar


31
LG:1400608.1:2000SEP08
g12052731
1.00E−175


Homo sapiens








mRNA; cDNA






DKFZp761G18121






(from clone






DKFZp761G18121);


32
LG:399275.5:2000SEP08
g14042034
0


Homo sapiens








cDNA FLJ14486 fis,






clone






MAMMA1002650,






weakly similar to


33
LG:293943.1:2000SEP08
g7022603
2.00E−24
(fl)(Homo sapiens)






unnamed protein


34
LG:345884.1:2000SEP08
g13591711
0


Homo sapiens








immunoglobulin






receptor






translocation






associated protein






2b (IRTA2) mRNA,


35
LG:400967.1:2000SEP08
g10047182
1.00E−176


Homo sapiens








mRNA for KIAA1559






protein, partial cds.


36
LG:024556.6:2000SEP08
g11999276
0


Homo sapiens








solute carrier






(SLC25A18) mRNA,






complete cds;






nuclear gene for


37
LG:081189.3:2000SEP08
g14325768
0


Homo sapiens








mRNA for KIAA1776






protein (fibrillin3),


38
LG:018258.1:2000SEP08
g12832288
3.00E−97
0(Mus musculus)


39
LG:450399.3:2000SEP08
g13097599
1.00E−10


Homo sapiens
,







Similar to ribosomal






protein L23, clone






IMAGE: 3606198,


40
LG:451122.1:2000SEP08
g6002102
2.00E−38
(fl)(Digitalis lanata)






Acyl-CoA binding






protein (ACBP)


41
LG:451682.1:2000SEP08
g8671496
1.00E−134
(fl)(Oryza sativa)






alpha 3 subunit of






20S proteasome


42
LG:238631.4:2000SEP08
g12803994
0


Homo sapiens
,







Similar to HLA class






II region expressed






gene KE2, clone






MGC: 4178, mRNA,


43
LG:236654.1:2000SEP08
g11558487
2.00E−08


Homo sapiens








mRNA for B-cell






lymphoma/leukaemia






11B (BCL11B


44
LG:332655.1:2000SEP08
g12856559
7.00E−93
0(Mus musculus)


45
LG:217396.2:2000SEP08
g10047294
0


Homo sapiens








mRNA for KIAA1610






protein, partial cds.


46
LG:090574.1:2000SEP08
g12845416
5.00E−37
0(Mus musculus)


47
LG:202943.1:2000SEP08
g12060829
0


Homo sapiens








serologically






defined breast






cancer antigen NY-






BR-38 mRNA,


48
LG:236928.1:2000SEP08
g14388574
0


Macaca










fascicularis
brain







cDNA clone: QtrA-


49
LG:215169.2:2000SEP08
g790349
1.00E−22


Homo sapiens








(clone NE68) gene


50
LG:410726.1:2000SEP08
g9963805
2.00E−17


Homo sapiens
zinc







finger protein






ZNF287 (ZNF287)


51
LG:234372.2:2000SEP08
g10436854
0


Homo sapiens








cDNA: FLJ20896 fis,






clone ADKA03527.


52
LG:022629.1:2000SEP08
g13879442
1.00E−178
(fl)(Mus musculus)






Similar to RIKEN






cDNA 2310035M22


53
LG:068682.1:2000SEP08
g13898616
0


Homo sapiens








serine/threonine






protein kinase SSTK






(SSTK) mRNA.


54
LG:222335.1:2000SEP08
g14250137
0


Homo sapiens
,







Similar to RIKEN






cDNA 5730421E18






gene, clone


55
LG:331342.1:2000SEP08
g10434081
0


Homo sapiens








cDNA FLJ12538 fis,






clone






NT2RM4000356,






moderately similar






to RAS-RELATED


56
LG:021770.1:2000SEP08
g9408105
2.00E−47


Homo sapiens
dNT-







2 gene for






mitochondrial 5′(3′)






deoxyribonucleotid


57
LG:181607.9:2000SEP08
g12834244
8.00E−91
0(Mus musculus)


58
LG:1042768.1:2000SEP08
g13937982
1.00E−180


Homo sapiens
,







translocase of inner






mitochondrial






membrane 17






(yeast) homolog A,






clone MGC: 14756,


59
LG:282729.1:2000SEP08
g12314268
1.00E−107
(5′ incom)(Homo








sapiens
) dJ14N1.2







(novel S-100/ICaBP






type calcium






binding domain


60
LG:998305.3:2000SEP08
g12053098
6.00E−88


Homo sapiens








mRNA; cDNA






DKFZp434A171






(from clone






DKFZp434A171);


61
LG:1135213.1:2000SEP08
g6692607
2.00E−69
(fl)(Mus musculus)






MGA protein


62
LG:267762.1:2000SEP08
g12854977
1.00E−135
0(Mus musculus)


63
LG:120744.1:2000SEP08
g12052773
0


Homo sapiens








mRNA; cDNA






DKFZp564B052






(from clone






DKFZp564B052);


64
LG:403409.1:2000SEP08
g8896163
0


Homo sapiens








kinesin-like protein






GAKIN mRNA,


65
LG:226874.3:2000SEP08
g3688393
3.00E−05


Homo sapiens








mRNA for triple LIM


66
LG:1045521.4:2000SEP08
g10436742
4.00E−58


Homo sapiens








cDNA FLJ14310 fis,






clone


67
LG:275876.1:2000SEP08
g5912051
6.00E−30
(3′ and 5′






incom)(Homo








sapiens
)



68
LG:475127.7:2000SEP08
g7294107
6.00E−44
(fl)(Drosophila








melanogaster
)







CG4638 gene


69
LG:157263.1:2000SEP08
g3047402
3.00E−40
(fl)(Homo sapiens)






monocarboxylate






transporter 2


70
LG:247382.7:2000SEP08
g4240292
5.00E−25


Homo sapiens








mRNA for KIAA0902






protein, complete


71
LG:197367.5:2000SEP08
g10172680
7.00E−14
(fl)(Bacillus








halodurans
) stage







V sporulation






protein C (peptidyl-


72
LG:218090.5:2000SEP08
g9295344
0


Homo sapiens








HSKM-B (HSKM-B)






mRNA, complete


73
LG:216612.4:2000SEP08
g8655677
0


Homo sapiens








mRNA; cDNA






DKFZp547M236






(from clone


74
LG:197614.1:2000SEP08
g13358641
0


Macaca










fascicularis
brain



75
LG:378428.1:2000SEP08
g7264026
0
(fl)(Homo sapiens)






dJ876B10.2 (novel






protein (ortholog of


76
LG:286639.1:2000SEP08
g13383264
0


Homo sapiens








mRNA for actin






related protein,


77
LG:389870.1:2000SEP08
g14388335
9.00E−63


Macaca










fascicularis
brain







cDNA clone: QflA-


78
LG:1387485.6:2000SEP08
g10435209
0


Homo sapiens








cDNA FLJ13261 fis,






clone






OVARC1000885,






weakly similar to






OXIDOREDUCTASE


79
LG:230151.1:2000SEP08
g8655647
0


Homo sapiens








mRNA; cDNA






DKFZp762M115






(from clone


80
LG:215158.5:2000SEP08
g10440162
0


Homo sapiens








cDNA: FLJ23465 fis,






clone HSI10904.


81
LG:235840.1:2000SEP08
g14042343
0


Homo sapiens








cDNA FLJ14666 fis,






clone






NT2RP2003000,






weakly similar to






TUMOR NECROSIS






FACTOR, ALPHA-


82
LG:350272.1:2000SEP08
g13477234
0


Homo sapiens
,







Similar to RIKEN






cDNA 0610037N03






gene, clone


83
LG:232190.1:2000SEP08
g10434968
1.00E−143


Homo sapiens








cDNA FLJ13105 fis,






clone






NT2RP3002351,






weakly similar to






Human mRNA for






NAD-dependent






methylene






tetrahydrofolate


84
LG:1068127.1:2000SEP08
g10436724
1.00E−140


Homo sapiens








cDNA FLJ14297 fis,






clone


85
LG:408751.3:2000SEP08
g8886024
0


Homo sapiens








collapsin response






mediator protein-5






(CRMP5) mRNA,


86
LG:1078933.1:2000SEP08
g14042843
0


Homo sapiens








cDNA FLJ14954 fis,






clone






PLACE3000169,






weakly similar to


87
LG:958731.1:2000SEP08
g9758769
6.00E−88
(fl) (Arabidopsis








thaliana
) 11-beta-







hydroxysteroid


88
LG:024125.5:2000SEP08
g12052958
0


Homo sapiens








mRNA; cDNA






DKFZp566J2046






(from clone






DKFZp566J2046);


89
LG:373637.3:2000SEP08
g11118740
0


Homo sapiens








UGT1 gene locus,






complete


90
LG:1053229.1:2000SEP08
g12804322
0


Homo sapiens
,







clone MGC: 4054,






mRNA, complete


91
LG:248364.1:2000SEP08
g12847599
0
0(Mus musculus)


92
LG:477130.1:2000SEP08
g6650751
1.00E−55
(fl)(Ceratopteris








richardii
) ribosomal



93
LG:113786.17:2000SEP08
g10440515
0


Homo sapiens








mRNA for FLJ00106






protein, partial cds.


94
LG:347635.1:2000SEP08
g11527996
0


Homo sapiens








NOTCH2 protein






(NOTCH2) mRNA,


95
LG:242966.4:2000SEP08
g9955987
0


Homo sapiens








clone






TCCCIA00164


96
LG:217814.1:2000SEP08
g10438977
0


Homo sapiens








cDNA: FLJ22551 fis,






clone HSI00804.


97
LG:476452.1:2000SEP08
g4126809
1.00E−121
(fl)(Oryza sativa)






glyoxalase I


98
LG:1100657.1:2000SEP08
g340298
1.00E−107
Human vasopressin






mRNA, complete


99
LG:1132418.2:2000SEP08
g12653472
2.00E−86


Homo sapiens
,







proteasome






(prosome,






macropain)






subunit, beta type,


100
LG:1098570.1:2000SEP08
g35069
1.00E−171


H. sapiens
RNA for







nm23-H2 gene.


101
LG:1097987.1:2000SEP08
g9368838
0


Homo sapiens








mRNA; cDNA






DKFZp547l014 (from






clone


102
LG:337818.2:2000SEP08
g14042395
0


Homo sapiens








cDNA FLJ14699 fis,






clone






NT2RP2006571,






moderately similar






to CYTOCHROME


103
LG:1040582.1:2000SEP08
g13529277
1.00E−119


Homo sapiens
,







aldo-keto






reductase family 1,






member A1






(aldehyde






reductase), clone


104
LG:1099122.1:2000SEP08
g13097716
8.00E−86


Homo sapiens
,







guanine






nucleotide binding






protein (G protein),






gamma 5, clone


105
LG:1327449.1:2000SEP08
g14042109
2.00E−96


Homo sapiens








cDNA FLJ14531 fis,






clone






NT2RM2000371,






weakly similar to






POLYRIBONUCLEOTIDE


106
LG:227933.5:2000SEP08
g9280028
0


Macaca










fascicularis
brain



107
LG:1043709.2:2000SEP08
g12804588
4.00E−30


Homo sapiens
,







Similar to CG9172






gene product,






clone MGC: 886,


108
LG:1099871.1:2000SEP08
g12652698
1.00E−154


Homo sapiens
,







purine-rich element






binding protein B,






clone MGC: 1947,


109
LG:1399139.4:2000SEP08
g10437077
0


Homo sapiens








cDNA: FLJ21069 fis,






clone CAS01594.


110
LG:236386.1:2000SEP08
g13477131
6.00E−87
(fl)(Homo sapiens)






SH3 and PX






domain-containing


111
LG:1015157.1:2000SEP08
g1881781
5.00E−72
glyoxalase I






(human, HeLa cells,






mRNA Partial, 572


112
LG:1065433.1:2000SEP08
g4589587
8.00E−29


Homo sapiens








mRNA for KIAA0972






protein, complete


113
LG:236992.4:2000SEP08
g12248381
0


Homo sapiens








mRNA for SEMB,


114
LG:1071124.1:2000SEP08
g13543418
0


Homo sapiens
,







Similar to zinc finger






protein 304, clone






MGC: 4079, mRNA,


115
LG:206425.2:2000SEP08
g12052883
2.00E−90


Homo sapiens








mRNA; cDNA






DKFZp564C2478






(from clone






DKFZp564C2478);


116
LG:885747.2:2000SEP08
g12804504
2.00E−49


Homo sapiens
,







Similar to ribosomal






protein L31, clone






MGC: 1641, mRNA,


117
LG:1140501.1:2000SEP08
g12052919
0


Homo sapiens








mRNA; cDNA






DKFZp564l1782






(from clone






DKFZp564l1782);


118
LG:001239.1:2000SEP08
g14164612
0


Homo sapiens
sialic







acid binding






immunoglobulin-






like lectin 10


119
LG:018980.1:2000SEP08
g10435149
0


Homo sapiens








cDNA FLJ13220 fis,






clone






NT2RP4002047,






moderately similar






to GTP-BINDING


120
LG:1083120.3:2000SEP08
g515786
3.00E−66


H. sapiens
(MAR7)







chromosome 19






DNA, 302bp.


121
LG:233258.3:2000SEP08
g10433125
0


Homo sapiens








cDNA FLJ11790 fis,






clone


122
LG:999062.1:2000SEP08
g9759463
3.00E−60
(fl)(Arabidopsis








thaliana
) 40S



123
LG:887776.1:2000SEP08
g342294
1.00E−66


Macaca mulatta








serum albumin


124
LG:1400301.2:2000SEP08
g12751104
1.00E−23


Homo sapiens








PNAS-130 mRNA,


125
LG:1329362.1:2000SEP08
g14042849
0


Homo sapiens








cDNA FLJ14959 fis,






clone






PLACE4000156,






moderately similar


126
LG:1096498.1:2000SEP08
g13097206
1.00E−110


Homo sapiens
,







ribosomal protein,






large, P1, clone






MGC: 5215, mRNA,


127
LG:1096337.1:2000SEP08
g13097206
1.00E−121


Homo sapiens
,







ribosomal protein,






large, P1, clone






MGC: 5215, mRNA,


128
LG:1400579.1:2000SEP08
g10437945
4.00E−61


Homo sapiens








cDNA: FLJ21781 fis,






clone HEP00223.


129
LG:1080091.1:2000SEP08
g10436724
1.00E−154


Homo sapiens








cDNA FLJ14297 fis,






clone


130
LG:1082203.1:2000SEP08
g10439929
0


Homo sapiens








cDNA: FLJ23296 fis,






clone HEP10656.


131
LG:1084051.1:2000SEP08
g6807586
1.00E−104
Novel human gene






mapping to






chomosome 1.


132
LG:1082393.1:2000SEP08
g10954043
0


Homo sapiens








KRAB zinc finger






protein ZFQR


133
LG:1086183.1:2000SEP08
g12655164
6.00E−58


Homo sapiens
, zinc







finger protein 256,






clone MGC: 1413,






mRNA, complete


134
LG:1090268.1:2000SEP08
g13938479
0


Homo sapiens
,







Similar to






hypothetical






protein FLJ22301,






clone


135
LG:1400597.5:2000SEP08
g14250145
1.00E−156


Homo sapiens
,







hypothetical






protein FLJ23407,






clone MGC: 14819,






mRNA, complete


136
LG:1080307.2:2000SEP08
g14043840
2.00E−34


Homo sapiens
,







clone MGC: 14429,






mRNA, complete


137
LG:1400603.2:2000SEP08
g4589565
4.00E−31


Homo sapiens








mRNA for KIAA0961






protein, complete


138
LG:1052984.1:2000SEP08
g13937998
0


Homo sapiens
,







Similar to DNA-






binding protein,






clone MGC: 14780,


139
LG:1091259.1:2000SEP08
g10436675
0


Homo sapiens








cDNA FLJ14260 fis,






clone






PLACE1001118.






weakly similar to


140
LG:1082263.2:2000SEP08
g13560887
5.00E−13


Homo sapiens
EZFIT-







related protein 1






mRNA, complete


141
LG:1048604.2:2000SEP08
g14249843
6.00E−67


Homo sapiens
,







Similar to






hypothetical






protein FLJ23233,






clone MGC: 14876,


142
LG:1085254.3:2000SEP08
g10437559
0


Homo sapiens








cDNA: FLJ21457 fis,






clone COL04705.


143
LG:1400606.2:2000SEP08
g14042549
9.00E−54


Homo sapiens








cDNA FLJ14779 fis,






clone






NT2RP4000398,






moderately similar


144
LG:1090358.2:2000SEP08
g10047182
6.00E−30


Homo sapiens








mRNA for KIAA1559






protein, partial cds.


145
LG:1079064.2:2000SEP08
g10434649
0


Homo sapiens








cDNA FLJ12895 fis,






clone






NT2RP2004187,






weakly similar to


146
LG:1076866.1:2000SEP08
g10436460
0


Homo sapiens








cDNA FLJ14087 fis,






clone






MAMMA1000183,






weakly similar to


147
LG:969359.1:2000SEP08
g13279004
1.00E−120


Homo sapiens
,







ferritin, light






polypeptide, clone






MGC: 10465, mRNA,


148
LG:366783.1:2000SEP08
g9651703
0


Homo sapiens








carboxypeptidase






B precursor (CPAH)






mRNA, complete


149
LG:332176.3:2000SEP08
g13365900
0


Macaca










fascicularis
brain







cDNA clone: QflA-


150
LG:994938.1:2000SEP08
g7023331
1.00E−76


Homo sapiens








cDNA FLJ10961 fis,






clone






PLACE1000588,






highly similar to






INTERFERON-


151
LG:982800.1:2000SEP08
g12053280
0


Homo sapiens








mRNA; cDNA






DKFZp434J037






(from clone






DKFZp434J037);


152
LG:977850.7:2000SEP08
g10436959
5.00E−64


Homo sapiens








cDNA: FLJ20984 fis,






clone CAE00871.


153
LG:234748.2:2000SEP08
g13182754
0


Homo sapiens








HPHRP mRNA,


154
LG:306284.1:2000SEP08
g14043648
0


Homo sapiens
,







clone MGC: 14161,






mRNA, complete


155
LI:333170.3:2000SEP08
g12314083
1.00E−93
(fl)(Homo sapiens)






dJ1007G16.5 (novel






high-mobility group






(nonhistone






chromosomal)


156
LI:336685.2:2000SEP08
g12697317
0


Homo sapiens








partial mRNA for


157
LI:279013.5:2000SEP08
g12840673
3.00E−55
0(Mus musculus)


158
LI:1037075.1:2000SEP08
g11342540
0


Homo sapiens








mRNA for putative






white family ATP-






binding cassette






transporter (ABCG4


159
LI:1073403.1:2000SEP08
g12804680
9.00E−63


Homo sapiens
,







S100 calcium-






binding protein,






beta (neural),






clone MGC: 1323,


160
LI:1075296.1:2000SEP08
g12803084
1.00E−112


Homo sapiens
,







mitochondrial






ribosomal protein






L12, clone






MGC: 8610, mRNA,


161
LI:1085501.1:2000SEP08
g12653784
1.00E−140


Homo sapiens
,







clone






IMAGE: 3349601,


162
LI:1086181.1:2000SEP08
g3043444
1.00E−146


Homo sapiens








mRNA for EDF-1


163
LI:1164493.1:2000SEP08
g13436439
0


Homo sapiens
,







clone MGC: 4400,






mRNA, complete


164
LI:1175097.1:2000SEP08
g13937908
4.00E−45


Homo sapiens
,







Similar to KIAA0961






protein, clone






MGC: 12515, mRNA,


165
LI:1092948.1:2000SEP08
g12804414
2.00E−49


Homo sapiens
,







Similar to






hypothetical






protein FLJ10891,






clone MGC: 925,


166
LI:380378.2:2000SEP08
g8655612
3.00E−79


Homo sapiens








mRNA; cDNA






DKFZp762O1415






(from clone


167
LI:1029674.1:2000SEP08
g9651088
4.00E−07


Macaca










fascicularis
brain



168
LI:2048601.3:2000SEP08
g10434880
1.00E−106


Homo sapiens








cDNA FLJ13048 fis,






clone






NT2RP3001399,






weakly similar to


169
LI:1186208.1:2000SEP08
g12052731
1.00E−175


Homo sapiens








mRNA; cDNA






DKFZp761G18121






(from clone






DKFZp761G18121);


170
LI:1170753.1:2000SEP08
g14249995
1.00E−101


Homo sapiens
,







clone MGC: 12518,






mRNA, complete


171
LI:1180908.1:2000SEP08
g14042849
0


Homo sapiens








cDNA FLJ14959 fis,






clone






PLACE4000156,






moderately similar


172
LI:1182900.2:2000SEP08
g10047304
0


Homo sapiens








mRNA for KIAA1615






protein, partial cds.


173
LI:1169548.2:2000SEP08
g14017832
0


Homo sapiens








mRNA for KIAA1808






protein, partial cds.


174
LI:1039974.1:2000SEP08
g13366083
0


Homo sapiens








MARKL1 mRNA for






MAP/microtubule






affinity-regulating






kinase like 1,


175
LI:1175765.2:2000SEP08
g13752753
5.00E−16


Homo sapiens
zinc







finger 1111 mRNA,






complete cds.


176
LI:313948.1:2000SEP08
g9651098
0


Macaca










fascicularis
brain



177
LI:335923.2:2000SEP08
g11990770
3.00E−73
(fl)(Homo sapiens)






bA534G20.1.1






(novel protein






similar to Lysozyme






C-1 (1,4-beta-N-






acylmuramidase C,


178
LI:345884.1:2000SEP08
g13591713
0


Homo sapiens








immunoglobulin






receptor






translocation






associated protein






2c (IRTA2) mRNA,


179
LI:417127.1:2000SEP08
g12652726
1.00E−66


Homo sapiens
,







clone






IMAGE: 3352566,


180
LI:451710.1:2000SEP08
g13899057
1.00E−61
(fl)(Mercurialis








annua
) ribosomal



181
LI:406882.2:2000SEP08
g7019948
2.00E−57


Homo sapiens








cDNA FLJ20081 fis,






clone COL03242.


182
LI:728223.1:2000SEP08
g2624328
2.00E−44
(fl)(Oryza sativa)


183
LI:289783.19:2000SEP08
g12654714
0


Homo sapiens
,







Similar to glucose






regulated protein,






58 kDa, clone


184
LI:235255.8:2000SEP08
g12597311
0


Homo sapiens








clone IMAGE: 72154






tRNA-guanine






transglycosylase






(TGT) mRNA,


185
LI:237693.5:2000SEP08
g12406772
4.00E−52
(fl)(Homo sapiens)






unnamed protein


186
LI:433670.3:2000SEP08
g14133250
0


Homo sapiens








mRNA for KIAA1479






protein, partial cds.


187
LI:202943.4:2000SEP08
g12060829
0


Homo sapiens








serologically






defined breast






cancer antigen NY-






BR-38 mRNA,


188
LI:068682.1:2000SEP08
g13540325
0


Homo sapiens








serine/threonine






kinase FKSG82






(FKSG82) mRNA,


189
LI:203301.3:2000SEP08
g10047160
0


Homo sapiens








mRNA for KIAA1548






protein, partial cds.


190
LI:020726.3:2000SEP08
g12834087
1.00E−157
0(Mus musculus)


191
LI:027209.1:2000SEP08
g13159480
1.00E−127
(fl)(Homo sapiens)






Translation may






initiate at the ATG






codon at






nucleotides 40-42


192
LI:108819.1:2000SEP08
g12052773
0


Homo sapiens








mRNA; cDNA






DKFZp564B052






(from clone






DKFZp564B052);


193
LI:021759.1:2000SEP08
g12006103
0


Homo sapiens
IRA1







mRNA, complete






cds, alternatively


194
LI:1165967.1:2000SEP08
g13529103
1.00E−172


Homo sapiens
,







ribosomal protein






S27a, clone






MGC: 12414, mRNA,


195
LI:1166315.1:2000SEP08
g12653800
1.00E−116


Homo sapiens
,







peptidylprolyl






isomerase A






(cyclophilin A),






clone MGC: 2351,


196
LI:204626.1:2000SEP08
g12844770
1.00E−138
0(Mus musculus)


197
LI:801140.1:2000SEP08
g12804322
0


Homo sapiens
,







clone MGC: 4054,






mRNA, complete


198
LI:286639.1:2000SEP08
g13938318
0


Homo sapiens
,







clone MGC: 15664,






mRNA, complete


199
LI:288905.4:2000SEP08
g12698056
0


Homo sapiens








mRNA for KIAA1756






protein, partial cds.


200
LI:332161.1:2000SEP08
g14388335
2.00E−62


Macaca










fascicularis
brain







cDNA clone: QflA-


201
LI:184867.1:2000SEP08
g7209586
4.00E−47
(fl)(Rattus








norvegicus
) DA41



202
LI:229932.4:2000SEP08
g10438187
0


Homo sapiens








cDNA: FLJ21963 fis,






clone HEP05583.


203
LI:1189932.1:2000SEP08
g12483887
0


Homo sapiens








solute carrier 19A3






mRNA, complete


204
LI:1076689.1:2000SEP08
g12804758
6.00E−20


Homo sapiens
,







ribonuclease 6






precursor, clone






MGC: 3554, mRNA,


205
LI:415181.2:2000SEP08
g11762100
0
(fl)(Zea mays) myoinositol






1-


206
LI:296358.1:2000SEP08
g12053148
0


Homo sapiens








mRNA; cDNA






DKFZp434G2226






(from clone






DKFZp434G2226);


207
LI:205186.3:2000SEP08
g567232
4.00E−17
(fl)(Mus musculus)






proline-rich protein


208
LI:220537.2:2000SEP08
g13365896
0


Macaca










fascicularis
brain







cDNA clone: QflA-


209
LI:248364.2:2000SEP08
g12847599
0
0(Mus musculus)


210
LI:2048338.1:2000SEP08
g12848905
3.00E−78
0(Mus musculus)


211
LI:1185203.8:2000SEP08
g11231084
3.00E−85


Macaca










fascicularis
brain



212
LI:021770.3:2000SEP08
g5931541
2.00E−45


Homo sapiens








genomic DNA,






chromosome






22q11.2, BCRL2


213
LI:1185841.1:2000SEP08
g14269501
0


Homo sapiens








unconventional






myosin 1G valine






form (MYO1G)






mRNA, MYO1G-V


214
LI:1181710.1:2000SEP08
g7959206
2.00E−49


Homo sapiens








mRNA for KIAA1473






protein, partial cds.


215
LI:2048959.1:2000SEP08
g5817101
1.00E−16


Homo sapiens








mRNA; cDNA






DKFZp434G1621






(from clone


216
LI:798494.1:2000SEP08
g10047182
2.00E−23


Homo sapiens








mRNA for KIAA1559






protein, partial cds.


217
LI:2049223.1:2000SEP08
g7959206
2.00E−43


Homo sapiens








mRNA for KIAA1473






protein, partial cds.


218
LI:1177833.1:2000SEP08
g12052982
0


Homo sapiens








mRNA; cDNA






DKFZp434l1610






(from clone






DKFZp434l1610);


219
LI:2049267.1:2000SEP08
g515786
6.00E−61


H. sapiens
(MAR7)







chromosome 19






DNA, 302bp.


220
LI:1165939.1:2000SEP08
g7020753
9.00E−13


Homo sapiens








cDNA FLJ20562 fis,






clone KAT11992.


221
LI:1170958.1:2000SEP08
g5262556
1.00E−14


Homo sapiens








mRNA; cDNA






DKFZp569D2231






(from clone






DKFZp569D2231);


222
LI:1089827.1:2000SEP08
g14042292
0


Homo sapiens








cDNA FLJ14636 fis,






clone






NT2RP2001233,






weakly similar to


223
LI:792112.1:2000SEP08
g10437945
4.00E−61


Homo sapiens








cDNA: FLJ21781 fis,






clone HEP00223.


224
LI:282219.2:2000SEP08
g12656630
7.00E−63


Homo sapiens








Kruppel-like zinc






finger protein GLIS2






mRNA, complete


225
LI:1088010.2:2000SEP08
g13623632
0


Homo sapiens
,







clone MGC: 13105,






mRNA, complete


226
LI:1165276.1:2000SEP08
g6807586
1.00E−106
Novel human gene






mapping to






chomosome 1.


227
LI:1169524.2:2000SEP08
g10047182
5.00E−30


Homo sapiens








mRNA for KIAA1559






protein, partial cds.


228
LI:1180255.1:2000SEP08
g14017870
0


Homo sapiens








mRNA for KIAA1827






protein, partial cds.


229
LI:1091903.1:2000SEP08
g14042372
2.00E−49


Homo sapiens








cDNA FLJ14686 fis,






clone






NT2RP2004961,






moderately similar






to Rattus








norvegicus








KRAB/zinc finger


230
LI:1169219.1:2000SEP08
g13937998
0


Homo sapiens
,







Similar to DNA-






binding protein,






clone MGC: 14780,


231
LI:2050313.1:2000SEP08
g12862319
0


Homo sapiens








mRNA for WDC146,


232
LI:209351.3:2000SEP08
g14042794
0


Homo sapiens








cDNA FLJ14923 fis,






clone






PLACE1008244,






weakly similar to






VEGETATIBLE


233
LI:119900.1:2000SEP08
g14042821
2.00E−66


Homo sapiens








cDNA FLJ14939 fis,






clone






PLACE1010702,






moderately similar


234
LI:2052274.1:2000SEP08
g8698839
4.00E−07


Homo sapiens








genomic DNA,






chromosome 8q23,


235
LI:1075502.1:2000SEP08
g13960141
1.00E−114


Homo sapiens
,







uridine






monophosphate






synthetase (orotate






phosphoribosyl






transferase and






orotidine-5′-






decarboxylase),


236
LI:813697.1:2000SEP08
g7020744
6.00E−59


Homo sapiens








cDNA FLJ20557 fis,






clone KAT11869.


237
LI:814261.1:2000SEP08
g7023331
1.00E−76


Homo sapiens








cDNA FLJ10961 fis,






clone






PLACE1000588,






highly similar to






INTERFERON-


238
LI:775334.1:2000SEP08
g4589587
3.00E−23


Homo sapiens








mRNA for KIAA0972






protein, complete


239
LI:1180325.1:2000SEP08
g10438159
0


Homo sapiens








cDNA: FLJ21941 fis,






clone HEP04524.


240
LI:1183147.3:2000SEP08
g10440084
0


Homo sapiens








cDNA: FLJ23407 fis,






clone HEP19601.


241
LI:1175373.3:2000SEP08
g7243242
5.00E−51


Homo sapiens








mRNA for KIAA1431






protein, partial cds.


242
LI:813757.1:2000SEP08
g4589587
1.00E−31


Homo sapiens








mRNA for KIAA0972






protein, complete


243
LI:1182979.2:2000SEP08
g14042292
2.00E−87


Homo sapiens








cDNA FLJ14636 fis,






clone






NT2RP2001233,






weakly similar to


244
LI:1177823.2:2000SEP08
g12052982
0


Homo sapiens








mRNA; cDNA






DKFZp434l1610






(from clone






DKFZp434l1610);


245
LI:1174279.1:2000SEP08
g10047182
1.00E−27


Homo sapiens








mRNA for KIAA1559






protein, partial cds.


246
LI:1178411.1:2000SEP08
g14042843
0


Homo sapiens








cDNA FLJ14954 fis,






clone






PLACE3000169,






weakly similar to


247
LI:1182739.1:2000SEP08
g12655164
8.00E−31


Homo sapiens
, zinc







finger protein 256,






clone MGC: 1413,






mRNA, complete


248
LI:234937.4:2000SEP08
g12804418
0


Homo sapiens
,







clone MGC: 1136,






mRNA, complete


249
LI:1170660.1:2000SEP08
g14388419
0


Macaca










fascicularis
brain







cDNA clone: QmoA-


250
LI:1144409.1:2000SEP08
g12053280
0


Homo sapiens








mRNA; cDNA






DKFZp434J037






(from clone






DKFZp434J037);


251
LI:246290.10:2000SEP08
g10438695
0


Homo sapiens








cDNA: FLJ22347 fis,






clone HRC06188.


252
LI:280034.1:2000SEP08
g12847023
1.00E−132
0(Mus musculus)










[0302]

4












TABLE 3








SEQ ID NO:
Template ID
Start
Stop
Frame
Pfam Hit
Pfam Description
E-value






















1
LG:150318.1:2000SEP08
11
79
forward 2
zf-C2H2
Zinc finger, C2H2 type
2.00E−06


2
LG:022529.1:2000SEP08
426
701
forward 3
C2
C2 domain
3.30E−06


3
LG:352559.1:2000SEP08
125
313
forward 2
KRAB
KRAB box
1.60E−41


4
LG:175223.1:2000SEP08
210
431
forward 3
CSD
‘Cold-shock’ DNA-binding domain
1.40E−18


5
LG:476989.1:2000SEP08
149
223
forward 2
zf-C3HC4
Zinc finger, C3HC4 type (RING finger)
3.00E−10


6
LG:253268.7:2000SEP08
211
435
forward 1
rrm
RNA recognition motif. (a.k.a. RRM,
3.50E−16








RBD, or RNP domain)


7
LG:401322.1:2000SEP08
156
341
forward 3
tubulin
Tubulin/FtsZ family
7.10E−20


7
LG:401322.1:2000SEP08
371
478
forward 2
tubulin
Tubulin/FtsZ family
2.50E−06


8
LG:1328436.1:2000SEP08
134
322
forward 2
KRAB
KRAB box
1.70E−42


9
LG:475404.1:2000SEP08
176
328
forward 2
KRAB
KRAB box
1.10E−15


10
LG:1384132.1:2000SEP08
157
225
forward 1
zf-C2H2
Zinc finger, C2H2 type
9.00E−04


11
LG:410804.18:2000SEP08
133
243
forward 1
pkinase
Protein kinase domain
7.90E−04


12
LG:1082306.1:2000SEP08
199
378
forward 1
KRAB
KRAB box
4.90E−20


12
LG:1082306.1:2000SEP08
559
627
forward 1
zf-C2H2
Zinc finger, C2H2 type
9.60E−05


13
LG:233814.4:2000SEP08
624
947
forward 3
mito_carr
Mitochondrial carrier protein
2.50E−04


14
LG:977478.5:2000SEP08
351
449
forward 3
ank
Ank repeat
1.10E−08


15
LG:025931.1:2000SEP08
660
728
forward 3
zf-C2H2
Zinc finger, C2H2 type
4.50E−06


15
LG:025931.1:2000SEP08
29
97
forward 2
zf-C2H2
Zinc finger, C2H2 type
7.20E−06


16
LG:885368.1:2000SEP08
133
462
forward 1
Ribosomal_S8
Ribosomal protein S8
7.50E−48


17
LG:1054900.1:2000SEP08
78
218
forward 3
KRAB
KRAB box
2.30E−17


18
LG:995186.2:2000SEP08
151
357
forward 1
KRAB
KRAB box
1.10E−04


19
LG:435048.23:2000SEP08
2
457
forward 2
Peptidase_M17
Cytosol aminopeptidase family,
5.30E−09








catalytic domain


20
LG:954859.1:2000SEP08
245
565
forward 2
Ribosomal_L7Ae
Ribosomal protein
7.80E−17








L7Ae/L30e/S12e/Gadd45 family


21
LG:364370.1:2000SEP08
42
578
forward 3
Ribosomal_L13e
Ribosomal protein L13e
2.30E−137


22
LG:1098789.1:2000SEP08
45
131
forward 3
efhand
EF hand
8.70E−05


23
LG:201540.2:2000SEP08
479
604
forward 2
zf-B_box
B-box zinc finger.
9.60E−14


23
LG:201540.2:2000SEP08
254
385
forward 2
zf-C3HC4
Zinc finger, C3HC4 type (RING finger)
4.80E−13


24
LG:1077357.1:2000SEP08
94
282
forward 1
KRAB
KRAB box
4.80E−31


25
LG:1048846.4:2000SEP08
60
245
forward 3
KRAB
KRAB box
7.10E−39


26
LG:336685.1:2000SEP08
945
1121
forward 3
homeobox
Homeobox domain
3.10E−11


27
LG:1076253.1:2000SEP08
6
188
forward 3
KRAB
KRAB box
4.10E−14


27
LG:1076253.1:2000SEP08
939
1007
forward 3
zf-C2H2
Zinc finger, C2H2 type
9.30E−06


28
LG:1400601.2:2000SEP08
38
106
forward 2
zf-C2H2
Zinc finger, C2H2 type
1.50E−05


29
LG:1079092.3:2000SEP08
314
382
forward 2
zf-C2H2
Zinc finger, C2H2 type
8.80E−06


30
LG:1086064.1:2000SEP08
128
316
forward 2
KRAB
KRAB box
2.00E−34


31
LG:1400608.1:2000SEP08
138
326
forward 3
KRAB
KRAB box
1.30E−40


32
LG:399275.5:2000SEP08
328
645
forward 1
BTB
BTB/POZ domain
4.10E−18


33
LG:293943.1:2000SEP08
265
327
forward 1
IQ
IQ calmodulin-binding motif
5.10E−04


34
LG:345884.1:2000SEP08
203
355
forward 2
ig
Immunoglobulin domain
7.40E−04


35
LG:400967.1:2000SEP08
109
300
forward 1
KRAB
KRAB box
1.50E−35


36
LG:024556.6:2000SEP08
526
774
forward 1
mito_carr
Mitochondrial carrier protein
2.90E−19


37
LG:081189.3:2000SEP08
362
475
forward 2
EGF
EGF-like domain
3.80E−06


38
LG:018258.1:2000SEP08
174
605
forward 3
Nitroreductase
Nitroreductase family
9.00E−05


39
LG:450399.3:2000SEP08
81
446
forward 3
Ribosomal_L14
Ribosomal protein L14p/L23e
1.20E−53


40
LG:451122.1:2000SEP08
49
303
forward 1
ACBP
Acyl CoA binding protein
1.70E−51


41
LG:451682.1:2000SEP08
117
560
forward 3
proteasome
Proteasome A-type and B-type
4.40E−59


42
LG:238631.4:2000SEP08
100
453
forward 1
KE2
KE2 family protein
3.80E−38


43
LG:236654.1:2000SEP08
810
878
forward 3
zf-C2H2
Zinc finger, C2H2 type
1.20E−04


43
LG:236654.1:2000SEP08
434
502
forward 2
zf-C2H2
Zinc finger, C2H2 type
6.60E−04


44
LG:332655.1:2000SEP08
415
513
forward 1
ank
Ank repeat
3.10E−10


45
LG:217396.2:2000SEP08
679
882
forward 1
ELM2
ELM2 domain
5.00E−14


45
LG:217396.2:2000SEP08
994
1134
forward 1
myb_DNA-binding
Myb-like DNA-binding domain
2.00E−11


46
LG:090574.1:2000SEP08
33
245
forward 3
carb_anhydrase
Eukaryotic-type carbonic anhydrase
3.10E−31


47
LG:202943.1:2000SEP08
199
360
forward 1
sushi
Sushi domain (SCR repeat)
3.80E−18


48
LG:236928.1:2000SEP08
259
1101
forward 1
GNS1_SUR4
GNS1/SUR4 family
9.80E−09


49
LG:215169.2:2000SEP08
89
208
forward 2
Idl_recept_a
Low-density lipoprotein receptor
1.00E−12








domain class A


50
LG:410726.1:2000SEP08
724
912
forward 1
KRAB
KRAB box
2.10E−17


50
LG:410726.1:2000SEP08
352
636
forward 1
SCAN
SCAN domain
8.90E−55


51
LG:234372.2:2000SEP08
557
862
forward 2
PH
PH domain
3.00E−09


51
LG:234372.2:2000SEP08
950
1408
forward 2
RhoGAP
RhoGAP domain
3.30E−39


51
LG:234372.2:2000SEP08
1952
2119
forward 2
SH3
SH3 domain
4.60E−11


52
LG:022629.1:2000SEP08
261
410
forward 3
zf-C3HC4
Zinc finger, C3HC4 type (RING finger)
2.00E−07


53
LG:068682.1:2000SEP08
176
883
forward 2
pkinase
Protein kinase domain
1.70E−65


54
LG:222335.1:2000SEP08
7
732
forward 1
DUF71
Domain of unknown function DUF71
6.70E−83


55
LG:331342.1:2000SEP08
558
1076
forward 3
arf
ADP-ribosylation factor family
1.20E−04


55
LG:331342.1:2000SEP08
588
1154
forward 3
ras
Ras family
2.60E−79


56
LG:021770.1:2000SEP08
228
1199
forward 3
adh_zinc
Zinc-binding dehydrogenases
7.80E−20


57
LG:181607.9:2000SEP08
161
604
forward 2
Josephin
Josephin
5.00E−50


58
LG:1042768.1:2000SEP08
42
443
forward 3
Tim17
Mitochondrial import inner membrane
1.40E−82








translocase subunit Tim17


59
LG:282729.1:2000SEP08
61
192
forward 1
S_100
S-100/ICaBP type calcium binding
1.10E−12








domain


60
LG:998305.3:2000SEP08
266
364
forward 2
ank
Ank repeat
2.10E−07


61
LG:1135213.1:2000SEP08
340
531
forward 1
T-box
T-box
8.80E−27


62
LG:267762.1:2000SEP08
64
1125
forward 1
A_deaminase
Adenosine/AMP deaminase
7.80E−20


63
LG:120744.1:2000SEP08
301
813
forward 1
vwa
von Willebrand factor type A domain
1.90E−52


64
LG:403409.1:2000SEP08
1458
1652
forward 3
FHA
FHA domain
3.00E−04


64
LG:403409.1:2000SEP08
78
1193
forward 3
kinesin
Kinesin motor domain
6.80E−172


65
LG:226874.3:2000SEP08
118
291
forward 1
LIM
LIM domain
8.40E−13


66
LG:1045521.4:2000SEP08
160
1464
forward 1
aminotran_1
Aminotransferase class-I
2.00E−10


67
LG:275876.1:2000SEP08
508
831
forward 1
CH
Calponin homology (CH) domain
2.40E−26


68
LG:475127.7:2000SEP08
169
498
forward 1
GTP_EFTU
Elongation factor Tu family
2.20E−46


69
LG:157263.1:2000SEP08
163
1314
forward 1
MCT
Monocarboxylate transporter
6.10E−31


70
LG:247382.7:2000SEP08
1105
1353
forward 1
PDZ
PDZ domain (Also known as DHR or
4.20E−07








GLGF).


70
LG:247382.7:2000SEP08
487
684
forward 1
SAM
SAM domain (Sterile alpha motif)
1.20E−11


71
LG:197367.5:2000SEP08
50
472
forward 2
Pept_tRNA_hydro
Peptidyl-tRNA hydrolase
8.90E−05


72
LG:218090.5:2000SEP08
179
295
forward 2
zf-MYND
MYND finger
3.00E−10


73
LG:216612.4:2000SEP08
138
1274
forward 3
Cation_efflux
Cation efflux family
8.90E−63


74
LG:197614.1:2000SEP08
1699
3048
forward 1
Oxysterol_BP
Oxysterol-binding protein
4.10E−31


74
LG:197614.1:2000SEP08
886
1164
forward 1
PH
PH domain
1.20E−14


75
LG:378428.1:2000SEP08
621
920
forward 3
PH
PH domain
2.00E−06


76
LG:286639.1:2000SEP08
1294
1713
forward 1
actin
Actin
9.10E−64


76
LG:286639.1:2000SEP08
630
1319
forward 3
actin
Actin
1.70E−62


77
LG:389870.1:2000SEP08
131
640
forward 2
ras
Ras family
3.40E−37


78
LG:1387485.6:2000SEP08
227
709
forward 2
adh_short
short chain dehydrogenase
1.10E−25


79
LG:230151.1:2000SEP08
631
1602
forward 1
E1_dehydrog
Dehydrogenase E1 component
1.10E−09


80
LG:215158.5:2000SEP08
1243
1377
forward 1
zf-AN1
AN1-like Zinc finger
9.10E−04


81
LG:235840.1:2000SEP08
1241
1537
forward 2
K_tetra
K+ channel tetramerisation domain
5.60E−22


82
LG:350272.1:2000SEP08
1424
1780
forward 2
SPRY
SPRY domain
2.10E−10


82
LG:350272.1:2000SEP08
557
682
forward 2
zf-C3HC4
Zinc finger, C3HC4 type (RING finger)
5.30E−11


83
LG:232190.1:2000SEP08
497
691
forward 2
zf-DHHC
DHHC zinc finger domain
2.30E−38


84
LG:1068127.1:2000SEP08
158
307
forward 2
KRAB
KRAB box
3.00E−12


85
LG:408751.3:2000SEP08
194
1204
forward 2
Dihydroorotase
Dihydroorotase-like
1.20E−12


85
LG:408751.3:2000SEP08
456
1355
forward 3
Dihydroorotase
Dihydroorotase-like
6.60E−08


86
LG:1078933.1:2000SEP08
373
441
forward 1
zf-C2H2
Zinc finger, C2H2 type
1.20E−07


86
LG:1078933.1:2000SEP08
689
775
forward 2
zf-C2H2
Zinc finger, C2H2 type
1.00E−03


87
LG:958731.1:2000SEP08
153
707
forward 3
adh_short
short chain dehydrogenase
2.40E−39


88
LG:024125.5:2000SEP08
132
635
forward 3
FAA_hydrolase
Fumarylacetoacetate (FAA) hydrolase
1.20E−83








family


89
LG:373637.3:2000SEP08
61
255
forward 1
DnaJ
DnaJ domain
7.40E−33


90
LG:1053229.1:2000SEP08
514
582
forward 1
zf-C2H2
Zinc finger, C2H2 type
2.50E−08


91
LG:248364.1:2000SEP08
253
594
forward 1
BTB
BTB/POZ domain
3.60E−04


91
LG:248364.1:2000SEP08
1544
1612
forward 2
zf-C2H2
Zinc finger, C2H2 type
7.10E−06


92
LG:477130.1:2000SEP08
174
554
forward 3
Ribosomal_L13
Ribosomal protein L13
3.60E−37


93
LG:113786.17:2000SEP08
134
376
forward 2
PDZ
PDZ domain (Also known as DHR or
8.10E−15








GLGF).


94
LG:347635.1:2000SEP08
315
410
forward 3
EGF
EGF-like domain
6.70E−09


94
LG:347635.1:2000SEP08
605
709
forward 2
EGF
EGF-like domain
1.10E−04


94
LG:347635.1:2000SEP08
1057
1152
forward 1
EGF
EGF-like domain
1.20E−04


95
LG:242966.4:2000SEP08
7
918
forward 1
aldedh
Aldehyde dehydrogenase family
1.10E−05


95
LG:242966.4:2000SEP08
1031
1993
forward 2
aldedh
Aldehyde dehydrogenase family
2.20E−05


96
LG:217814.1:2000SEP08
1167
1265
forward 3
ank
Ank repeat
6.60E−08


97
LG:476452.1:2000SEP08
210
581
forward 3
Glyoxalase
Glyoxalase/Bleomycln resistance
8.10E−39








protein/Dioxygenase superfamily


98
LG:1100657.1:2000SEP08
151
384
forward 1
hormone5
Neurohypophysial hormones, C-
8.60E−47








terminal Domain


99
LG:1132418.2:2000SEP08
109
393
forward 1
proteasome
Proteasome A-type and B-type
1.10E−14


100
LG:1098570.1:2000SEP08
129
572
forward 3
NDK
Nucleoside diphosphate kinases
3.70E−117


101
LG:1097987.1:2000SEP08
747
908
forward 3
Ribosomal_L23
Ribosomal protein L23
5.80E−14


102
LG:337818.2:2000SEP08
136
1518
forward 1
p450
Cytochrome P450
6.30E−175


103
LG:1040582.1:2000SEP08
266
556
forward 2
aldo_ket_red
Aldo/keto reductase family
1.30E−47


103
LG:1040582.1:2000SEP08
546
635
forward 3
aldo_ket_red
Aldo/keto reductase family
7.60E−06


104
LG:1099122.1:2000SEP08
84
248
forward 3
G-gamma
GGL domain
4.90E−31


105
LG:1327449.1:2000SEP08
461
526
forward 2
Ribosomal_S8
Ribosomal protein S8
4.80E−07


105
LG:1327449.1:2000SEP08
246
359
forward 3
Ribosomal_S8
Ribosomal protein S8
3.00E−06


106
LG:227933.5:2000SEP08
523
1455
forward 1
AMP-binding
AMP-binding enzyme
7.20E−05


107
LG:1043709.2:2000SEP08
457
723
forward 1
oxidored_q6
NADH ubiquinone oxidoreductase, 20 Kd
8.40E−08








subunit


108
LG:1099871.1:2000SEP08
34
411
forward 1
histone
Core histone H2A/H2B/H3/H4
4.50E−47


109
LG:1399139.4:2000SEP08
117
233
forward 3
CAP_GLY
CAP-Gly domain
4.30E−10


110
LG:236386.1:2000SEP08
1383
1712
forward 3
PX
PX domain
1.90E−13


111
LG:1015157.1:2000SEP08
115
552
forward 1
Glyoxalase
Glyoxalase/Bleomycin resistance
6.00E−38








protein/Dioxygenase superfamily


112
LG:1065433.1:2000SEP08
264
449
forward 3
KRAB
KRAB box
1.30E−38


113
LG:236992.4:2000SEP08
286
465
forward 1
Sema
Sema domain
2.70E−21


113
LG:236992.4:2000SEP08
209
292
forward 2
Sema
Sema domain
3.60E−06


114
LG:1071124.1:2000SEP08
469
630
forward 1
KRAB
KRAB box
1.20E−16


115
LG:206425.2:2000SEP08
109
519
forward 1
GBP
Guanylate-binding protein, N-terminal
1.60E−100








domain


115
LG:206425.2:2000SEP08
491
916
forward 2
GBP
Guanylate-binding protein, N-terminal
2.70E−70








domain


115
LG:206425.2:2000SEP08
1164
1685
forward 3
GBP_C
Guanylate-binding protein, C-terminal
3.50E−71








domain


115
LG:206425.2:2000SEP08
920
1201
forward 2
GBP_C
Guanylate-binding protein, C-terminal
3.10E−63








domain


115
LG:206425.2:2000SEP08
1651
1773
forward 1
GBP_C
Guanylate-binding protein, C-terminal
1.80E−04








domain


116
LG:885747.2:2000SEP08
372
569
forward 3
Ribosomal_L31e
Ribosomal protein L31e
9.50E−16


117
LG:1140501.1:2000SEP08
176
340
forward 2
ATP1G1_PLM
ATP1G1/PLM/MAT8 family
9.30E−22







MAT8


118
LG:001239.1:2000SEP08
1686
1850
forward 3
ig
Immunoglobulin domain
2.50E−08


118
LG:001239.1:2000SEP08
1391
1561
forward 2
ig
Immunoglobulin domain
4.00E−08


119
LG:018980.1:2000SEP08
395
502
forward 2
GTP_EFTU
Elongation factor Tu family
3.20E−09


119
LG:018980.1:2000SEP08
634
801
forward 1
GTP_EFTU
Elongation factor Tu family
3.50E−07


119
LG:018980.1:2000SEP08
159
215
forward 3
GTP_EFTU
Elongation factor Tu family
6.90E−07


120
LG:1083120.3:2000SEP08
117
266
forward 3
KRAB
KRAB box
5.10E−22


121
LG:233258.3:2000SEP08
1797
2069
forward 3
cadherin
Cadherin domain
3.90E−24


122
LG:999062.1:2000SEP08
78
497
forward 3
Ribosomal_S19e
Ribosomal protein S19e
2.10E−101


123
LG:887776.1:2000SEP08
101
625
forward 2
transport_prot
Serum albumin family
3.30E−92


123
LG:887776.1:2000SEP08
699
1163
forward 3
transport_prot
Serum albumin family
5.90E−41


124
LG:1400301.2:2000SEP08
253
441
forward 1
KRAB
KRAB box
2.10E−38


125
LG:1329362.1:2000SEP08
194
262
forward 2
zf-C2H2
Zinc finger, C2H2 type
3.90E−06


126
LG:1096498.1:2000SEP08
17
358
forward 2
60s_ribosomal
60s Acidic ribosomal protein
1.70E−48


127
LG:1096337.1:2000SEP08
512
637
forward 2
60s_ribosomal
60s Acidic ribosomal protein
4.10E−07


127
LG:1096337.1:2000SEP08
619
738
forward 1
60s_ribosomal
60s Acidic ribosomal protein
1.50E−04


128
LG:1400579.1:2000SEP08
200
268
forward 2
zf-C2H2
Zinc finger, C2H2 type
7.80E−05


129
LG:1080091.1:2000SEP08
151
318
forward 1
KRAB
KRAB box
1.80E−25


130
LG:1082203.1:2000SEP08
961
1029
forward 1
zf-C2H2
Zinc finger, C2H2 type
2.10E−08


131
LG:1084051.1:2000SEP08
195
263
forward 3
zf-C2H2
Zinc finger, C2H2 type
1.80E−06


132
LG:1082393.1:2000SEP08
237
425
forward 3
KRAB
KRAB box
1.80E−36


132
LG:1082393.1:2000SEP08
1251
1319
forward 3
zf-C2H2
Zinc finger, C2H2 type
1.40E−06


133
LG:1086183.1:2000SEP08
308
478
forward 2
KRAB
KRAB box
1.50E−15


133
LG:1086183.1:2000SEP08
833
901
forward 2
zf-C2H2
Zinc finger, C2H2 type
9.60E−07


134
LG:1090268.1:2000SEP08
1167
1235
forward 3
zf-C2H2
Zinc finger, C2H2 type
1.00E−07


135
LG:1400597.5:2000SEP08
63
131
forward 3
zf-C2H2
Zinc finger, C2H2 type
1.20E−04


136
LG:1080307.2:2000SEP08
108
239
forward 3
KRAB
KRAB box
3.60E−04


137
LG:1400603.2:2000SEP08
299
490
forward 2
KRAB
KRAB box
5.50E−41


137
LG:1400603.2:2000SEP08
929
997
forward 2
zf-C2H2
Zinc finger, C2H2 type
1.20E−04


138
LG:1052984.1:2000SEP08
142
330
forward 1
KRAB
KRAB box
3.70E−41


139
LG:1091259.1:2000SEP08
555
623
forward 3
zf-C2H2
Zinc finger, C2H2 type
1.20E−07


140
LG:1082263.2:2000SEP08
258
443
forward 3
KRAB
KRAB box
2.50E−29


140
LG:1082263.2:2000SEP08
981
1049
forward 3
zf-C2H2
Zinc finger, C2H2 type
1.70E−07


141
LG:1048604.2:2000SEP08
351
530
forward 3
KRAB
KRAB box
3.50E−20


142
LG:1085254.3:2000SEP08
746
814
forward 2
zf-C2H2
Zinc finger, C2H2 type
3.10E−07


143
LG:1400606.2:2000SEP08
244
432
forward 1
KRAB
KRAB box
7.60E−41


143
LG:1400606.2:2000SEP08
904
972
forward 1
zf-C2H2
Zinc finger, C2H2 type
1.80E−07


144
LG:1090358.2:2000SEP08
385
573
forward 1
KRAB
KRAB box
1.30E−47


144
LG:1090358.2:2000SEP08
862
930
forward 1
zf-C2H2
Zinc finger, C2H2 type
7.90E−07


145
LG:1079064.2:2000SEP08
325
612
forward 1
SCAN
SCAN domain
3.00E−39


146
LG:1076866.1:2000SEP08
203
391
forward 2
KRAB
KRAB box
6.20E−39


146
LG:1076866.1:2000SEP08
1868
1936
forward 2
zf-C2H2
Zinc finger, C2H2 type
5.20E−08


147
LG:969359.1:2000SEP08
221
715
forward 2
ferritin
Ferritin
3.10E−86


148
LG:366783.1:2000SEP08
70
609
forward 1
Zn_carbOpept
Zinc carboxypeptidase
8.80E−76


148
LG:366783.1:2000SEP08
705
806
forward 3
Zn_carbOpept
Zinc carboxypeptidase
2.20E−10


148
LG:366783.1:2000SEP08
623
724
forward 2
Zn_carbOpept
Zinc carboxypeptidase
1.80E−05


149
LG:332176.3:2000SEP08
5
1060
forward 2
Glyco_hydro_31
Glycosyl hydrolases family 31
2.40E−163


150
LG:994938.1:2000SEP08
3
95
forward 3
GBP
Guanylate-binding protein, N-terminal
4.20E−14








domain


151
LG:982800.1:2000SEP08
16
243
forward 1
pkinase
Protein kinase domain
1.30E−10


152
LG:977850.7:2000SEP08
7
102
forward 1
zf-DHHC
DHHC zinc finger domain
1.30E−04


153
LG:234748.2:2000SEP08
6
149
forward 3
PTE
Phosphotriesterase family
1.20E−19


154
LG:306284.1:2000SEP08
197
613
forward 2
Band_41
FERM domain (Band 4.1 family)
2.00E−52


155
LI:333170.3:2000SEP08
292
498
forward 1
HMG_box
HMG (high mobility group) box
1.80E−22


156
LI:336685.2:2000SEP08
913
1092
forward 1
homeobox
Homeobox domain
4.20E−15


157
LI:279013.5:2000SEP08
393
500
forward 3
WD40
WD domain, G-beta repeat
2.70E−05


158
LI:1037075.1:2000SEP08
322
666
forward 1
ABC_tran
ABC transporter
7.10E−04


158
LI:1037075.1:2000SEP08
328
375
forward 1
PRK
Phosphoribulokinase/Uridine kinase
7.40E−04








family


159
LI:1073403.1:2000SEP08
203
289
forward 2
efhand
EF hand
5.50E−04


159
LI:1073403.1:2000SEP08
56
187
forward 2
S_100
S-100/CaBP type calcium binding
3.60E−23








domain


160
LI:1075296.1:2000SEP08
337
543
forward 1
Ribosomal_L12
Ribosomal protein L7/L12 C-terminal
5.40E−09








domain


161
LI:1085501.1:2000SEP08
561
776
forward 3
EF1BD
EF-1 guanine nucleotide exchange
1.20E−24








domain


162
LI:1086181.1:2000SEP08
305
469
forward 2
HTH_3
Helix-turn-helix
1.20E−10


163
LI:1164493.1:2000SEP08
365
553
forward 2
KRAB
KRAB box
8.10E−31


164
LI:1175097.1:2000SEP08
460
648
forward 1
KRAB
KRAB box
7.60E−41


165
LI:1092948.1:2000SEP08
446
595
forward 2
KRAB
KRAB box
2.80E−21


166
LI:380378.2:2000SEP08
120
419
forward 3
mito_carr
Mitochondrial carrier protein
1.30E−25


167
LI:1029674.1:2000SEP08
360
431
forward 3
LRR
Leucine Rich Repeat
9.00E−04


168
LI:2048601.3:2000SEP08
2
145
forward 2
ig
Immunoglobulin domain
3.00E−05


169
LI:1186208.1:2000SEP08
161
349
forward 2
KRAB
KRAB box
1.30E−40


170
LI:1170753.1:2000SEP08
130
318
forward 1
KRAB
KRAB box
8.40E−42


171
LI:1180908.1:2000SEP08
509
577
forward 2
zf-C2H2
Zinc finger, C2H2 type
3.90E−06


171
LI:1180908.1:2000SEP08
340
408
forward 1
zf-C2H2
Zinc finger, C2H2 type
1.30E−04


172
LI:1182900.2:2000SEP08
346
414
forward 1
zf-C2H2
Zinc finger, C2H2 type
3.10E−07


173
LI:1169548.2:2000SEP08
393
500
forward 3
VHP
Villin headpiece domain
7.10E−20


174
LI:1039974.1:2000SEP08
191
742
forward 2
pkinase
Protein kinase domain
1.30E−37


175
LI:1175765.2:2000SEP08
279
446
forward 3
KRAB
KRAB box
5.20E−23


176
LI:313948.1:2000SEP08
75
143
forward 3
zf-C2H2
Zinc finger, C2H2 type
2.20E−07


177
LI:335923.2:2000SEP08
215
523
forward 2
lys
C-type lysozyme/alpha-lactalbumin
1.60E−42








family


178
LI:345884.1:2000SEP08
208
360
forward 1
ig
Immunoglobulin domain
7.40E−04


179
LI:417127.1:2000SEP08
359
529
forward 2
KRAB
KRAB box
4.90E−22


180
LI:451710.1:2000SEP08
130
459
forward 1
Ribosomal_L32e
Ribosomal protein L32
4.80E−57


181
LI:406882.2:2000SEP08
247
408
forward 1
Kelch
Kelch motif
4.20E−11


181
LI:406882.2:2000SEP08
656
793
forward 2
Kelch
Kelch motif
8.90E−09


182
LI:728223.1:2000SEP08
158
373
forward 2
rrm
RNA recognition motif. (a.k.a. RRM,
1.20E−28








RBD, or RNP domain)


183
LI:289783.19:2000SEP08
821
1003
forward 2
thiored
Thioredoxin
1.70E−20


183
LI:289783.19:2000SEP08
747
800
forward 3
thiored
Thioredoxin
5.10E−05


184
LI:235255.8:2000SEP08
419
919
forward 2
TGT
Queuine tRNA-ribosyltransferase
2.10E−24


184
LI:235255.8:2000SEP08
747
1346
forward 3
TGT
Queuine tRNA-ribosyltransferase
7.00E−15


185
LI:237693.5:2000SEP08
48
518
forward 3
abhydrolase_2
Phospholipase/Carboxylesterase
6.20E−07


186
LI:433670.3:2000SEP08
404
682
forward 2
Sema
Sema domain
3.80E−26


187
LI:202943.4:2000SEP08
119
223
forward 2
EGF
EGF-like domain
1.60E−05


187
LI:202943.4:2000SEP08
1304
1465
forward 2
sushi
Sushi domain (SCR repeat)
3.80E−18


188
LI:068682.1:2000SEP08
169
876
forward 1
pkinase
Protein kinase domain
1.70E−65


189
LI:203301.3:2000SEP08
570
716
forward 3
Band_41
FERM domain (Band 4.1 family)
1.50E−20


189
LI:203301.3:2000SEP08
365
577
forward 2
Band_41
FERM domain (Band 4.1 family)
6.30E−16


190
LI:020726.3:2000SEP08
542
1915
forward 2
MCT
Monocarboxylate transporter
1.80E−98


191
LI:027209.1:2000SEP08
379
987
forward 1
fibrinogen_C
Fibrinogen beta and gamma chains, C-
7.80E−43








terminal globular domain


192
LI:108819.1:2000SEP08
316
828
forward 1
vwa
von Willebrand factor type A domain
1.90E−52


193
LI:021759.1:2000SEP08
1136
1246
forward 2
WD40
WD domain, G-beta repeat
1.70E−07


194
LI:1165967.1:2000SEP08
322
462
forward 1
Ribosomal_S27
Ribosomal protein S27a
1.50E−30


194
LI:1165967.1:2000SEP08
22
243
forward 1
ubiquitin
Ubiquitin family
4.50E−42


195
LI:1166315.1:2000SEP08
131
283
forward 2
pro_isomerase
Cyclophilin type peptidyl-prolyl cis-
1.10E−26








trans isomerase


195
LI:1166315.1:2000SEP08
280
423
forward 1
pro_isomerase
Cyclophilin type peptidyl-prolyl cis-
5.50E−17








trans isomerase


195
LI:1166315.1:2000SEP08
423
482
forward 3
pro_isomerase
Cyclophilin type peptidyl-prolyl cis-
4.10E−06








trans isomerase


196
LI:204626.1:2000SEP08
322
1212
forward 1
Syntaxin
Syntaxin
8.60E−44


197
LI:801140.1:2000SEP08
516
584
forward 3
zf-C2H2
Zinc finger, C2H2 type
2.50E−08


198
LI:286639.1:2000SEP08
1295
1714
forward 2
actin
Actin
9.10E−64


198
LI:286639.1:2000SEP08
772
1296
forward 1
actin
Actin
1.60E−44


198
LI:286639.1:2000SEP08
630
755
forward 3
actin
Actin
1.10E−09


199
LI:288905.4:2000SEP08
285
602
forward 3
CH
Calponin homology (CH) domain
5.30E−27


200
LI:332161.1:2000SEP08
75
710
forward 3
ras
Ras family
2.00E−48


201
LI:184867.1:2000SEP08
365
478
forward 2
ubiquitin
Ubiquitin family
1.40E−04


202
LI:229932.4:2000SEP08
58
969
forward 1
AMP-binding
AMP-binding enzyme
3.00E−06


203
LI:1189932.1:2000SEP08
95
1441
forward 2
Folate_carrier
Reduced folate carrier
5.80E−10


204
LI:1076689.1:2000SEP08
346
708
forward 1
ribonuclease_T2
Ribonuclease T2 family
6.50E−19


205
LI:415181.2:2000SEP08
505
1584
forward 1
Inos-1-P_synth
Myo-inositol-1-phosphate synthase
2.30E−136


205
LI:415181.2:2000SEP08
294
1220
forward 3
Inos-1-P_synth
Myo-inositol-1-phosphate synthase
3.40E−16


206
LI:296358.1:2000SEP08
678
1061
forward 3
kinesin
Kinesin motor domain
1.40E−46


206
LI:296358.1:2000SEP08
163
510
forward 1
kinesin
Kinesin motor domain
6.80E−24


207
LI:205186.3:2000SEP08
476
982
forward 2
lactamase_B
Metallo-beta-lactamase superfamily
3.70E−06


208
LI:220537.2:2000SEP08
60
1574
forward 3
sugar_tr
Sugar (and other) transporter
6.40E−07


209
LI:248364.2:2000SEP08
253
594
forward 1
BTB
BTB/POZ domain
3.60E−04


209
LI:248364.2:2000SEP08
1544
1612
forward 2
zf-C2H2
Zinc finger, C2H2 type
7.10E−06


210
LI:2048338.1:2000SEP08
261
410
forward 3
zf-C3HC4
Zinc finger, C3HC4 type (RING finger)
2.00E−07


211
LI:1185203.8:2000SEP08
333
431
forward 3
ank
Ank repeat
2.20E−07


212
LI:021770.3:2000SEP08
287
1171
forward 2
adh_zinc
Zinc-binding dehydrogenases
3.70E−08


213
LI:1185841.1:2000SEP08
705
860
forward 3
myosin_head
Myosin head (motor domain)
1.80E−07


213
LI:1185841.1:2000SEP08
992
1063
forward 2
myosin_head
Myosin head (motor domain)
3.20E−04


214
LI:1181710.1:2000SEP08
62
130
forward 2
zf-C2H2
Zinc finger, C2H2 type
1.10E−05


215
LI:2048959.1:2000SEP08
225
293
forward 3
zf-C2H2
Zinc finger, C2H2 type
4.10E−07


216
LI:798494.1:2000SEP08
273
464
forward 3
KRAB
KRAB box
2.00E−42


216
LI:798494.1:2000SEP08
675
743
forward 3
zf-C2H2
Zinc finger, C2H2 type
4.50E−05


216
LI:798494.1:2000SEP08
794
862
forward 2
zf-C2H2
Zinc finger, C2H2 type
6.80E−04


217
LI:2049223.1:2000SEP08
130
318
forward 1
KRAB
KRAB box
2.10E−42


218
LI:1177833.1:2000SEP08
78
218
forward 3
KRAB
KRAB box
2.30E−17


218
LI:1177833.1:2000SEP08
999
1067
forward 3
zf-C2H2
Zinc finger, C2H2 type
1.70E−04


219
LI:2049267.1:2000SEP08
78
227
forward 3
KRAB
KRAB box
3.70E−22


220
LI:1165939.1:2000SEP08
247
315
forward 1
zf-C2H2
Zinc finger, C2H2 type
2.60E−06


221
LI:1170958.1:2000SEP08
397
465
forward 1
zf-C2H2
Zinc finger, C2H2 type
3.20E−07


222
LI:1089827.1:2000SEP08
722
790
forward 2
zf-C2H2
Zinc finger, C2H2 type
3.10E−07


222
LI:1089827.1:2000SEP08
105
173
forward 3
zf-C2H2
Zinc finger, C2H2 type
9.60E−07


222
LI:1089827.1:2000SEP08
433
501
forward 1
zf-C2H2
Zinc finger, C2H2 type
2.10E−06


223
LI:792112.1:2000SEP08
200
268
forward 2
zf-C2H2
Zinc finger, C2H2 type
7.80E−05


224
LI:282219.2:2000SEP08
129
197
forward 3
zf-C2H2
Zinc finger, C2H2 type
4.10E−05


225
LI:1088010.2:2000SEP08
294
362
forward 3
zf-C2H2
Zinc finger, C2H2 type
5.80E−08


226
LI:1165276.1:2000SEP08
195
263
forward 3
zf-C2H2
Zinc finger, C2H2 type
1.80E−06


227
LI:1169524.2:2000SEP08
267
455
forward 3
KRAB
KRAB box
2.70E−40


227
LI:1169524.2:2000SEP08
727
795
forward 1
zf-C2H2
Zinc finger, C2H2 type
7.90E−07


228
LI:1180255.1:2000SEP08
440
628
forward 2
KRAB
KRAB box
2.30E−33


228
LI:1180255.1:2000SEP08
1027
1095
forward 1
zf-C2H2
Zinc finger, C2H2 type
2.50E−07


229
LI:1091903.1:2000SEP08
182
370
forward 2
KRAB
KRAB box
6.20E−39


230
LI:1169219.1:2000SEP08
142
330
forward 1
KRAB
KRAB box
3.70E−41


231
LI:2050313.1:2000SEP08
803
982
forward 2
Collagen
Collagen triple helix repeat (20 copies)
9.50E−10


232
LI:209351.3:2000SEP08
561
671
forward 3
WD40
WD domain, G-beta repeat
2.20E−06


232
LI:209351.3:2000SEP08
313
423
forward 1
WD40
WD domain, G-beta repeat
1.00E−04


233
LI:119900.1:2000SEP08
179
358
forward 2
KRAB
KRAB box
1.50E−34


234
LI:2052274.1:2000SEP08
193
1197
forward 1
A_deaminase
Adenosine/AMP deaminase
4.00E−10


235
LI:1075502.1:2000SEP08
100
315
forward 1
OMPdecase
Orotidine 5′-phosphate decarboxylase
6.30E−35


235
LI:1075502.1:2000SEP08
305
451
forward 2
OMPdecase
Orotidine 5′-phosphate decarboxylase
4.70E−26


235
LI:1075502.1:2000SEP08
426
806
forward 3
OMPdecase
Orotidine 5′-phosphate decarboxylase
1.80E−12


236
LI:813697.1:2000SEP08
753
821
forward 3
zf-C2H2
Zinc finger, C2H2 type
1.60E−07


237
LI:814261.1:2000SEP08
3
95
forward 3
GBP
Guanylate-binding protein, N-terminal
4.20E−14








domain


238
LI:775334.1:2000SEP08
112
180
forward 1
zf-C2H2
Zinc finger, C2H2 type
2.10E−08


239
LI:1180325.1:2000SEP08
495
563
forward 3
zf-C2H2
Zinc finger, C2H2 type
2.20E−07


240
LI:1183147.3:2000SEP08
82
150
forward 1
zf-C2H2
Zinc finger, C2H2 type
1.20E−04


241
LI:1175373.3:2000SEP08
191
379
forward 2
KRAB
KRAB box
6.80E−45


242
LI:813757.1:2000SEP08
268
453
forward 1
KRAB
KRAB box
4.30E−38


243
LI:1182979.2:2000SEP08
341
409
forward 2
zf-C2H2
Zinc finger, C2H2 type
3.60E−06


244
LI:1177823.2:2000SEP08
1232
1372
forward 2
KRAB
KRAB box
3.00E−15


245
LI:1174279.1:2000SEP08
276
464
forward 3
KRAB
KRAB box
1.40E−46


245
LI:1174279.1:2000SEP08
753
821
forward 3
zf-C2H2
Zinc finger, C2H2 type
7.90E−07


246
LI:1178411.1:2000SEP08
787
855
forward 1
zf-C2H2
Zinc finger, C2H2 type
1.20E−07


247
LI:1182739.1:2000SEP08
582
650
forward 3
zf-C2H2
Zinc finger, C2H2 type
6.70E−08


248
LI:234937.4:2000SEP08
61
477
forward 1
DSPc
Dual specificity phosphatase, catalytic
8.70E−29








domain


249
LI:1170660.1:2000SEP08
35
103
forward 2
zf-C2H2
Zinc finger, C2H2 type
8.70E−07


250
LI:1144409.1:2000SEP08
16
243
forward 1
pkinase
Protein kinase domain
1.30E−10


251
LI:246290.10:2000SEP08
256
453
forward 1
rrm
RNA recognition motif. (a.k.a. RRM,
2.10E−08








RBD, or RNP domain)


252
LI:280034.1:2000SEP08
119
652
forward 2
AAA
ATPase family associated with various
1.80E−64








cellular activities (AAA)










[0303]

5











TABLE 4








SEQ ID NO:
Template ID
Start
Stop
Frame
Domain
Topology





















34
LG:345884.1:2000SEP08
56
142
forward 2
TM
N out


35
LG:400967.1:2000SEP08
470
547
forward 2
TM
N out


36
LG:024556.6:2000SEP08
529
597
forward 1
TM
N in


37
LG:081189.3:2000SEP08
627
686
forward 3
TM
N out


38
LG:018258.1:2000SEP08
430
507
forward 1
TM
N out


38
LG:018258.1:2000SEP08
444
503
forward 3
TM
N out


39
LG:450399.3:2000SEP08
145
231
forward 1
TM
N out


39
LG:450399.3:2000SEP08
417
503
forward 3
TM
N in


40
LG:451122.1:2000SEP08
328
390
forward 1
TM
N in


41
LG:451682.1:2000SEP08
93
155
forward 3
TM


42
LG:238631.4:2000SEP08
526
612
forward 1
TM
N out


42
LG:238631.4:2000SEP08
477
563
forward 3
TM


43
LG:236654.1:2000SEP08
236
295
forward 2
TM
N out


44
LG:332655.1:2000SEP08
541
621
forward 1
TM
N out


44
LG:332655.1:2000SEP08
536
598
forward 2
TM
N out


44
LG:332655.1:2000SEP08
626
688
forward 2
TM
N out


44
LG:332655.1:2000SEP08
887
949
forward 2
TM
N out


44
LG:332655.1:2000SEP08
965
1027
forward 2
TM
N out


44
LG:332655.1:2000SEP08
912
998
forward 3
TM
N out


45
LG:217396.2:2000SEP08
317
391
forward 2
TM
N out


45
LG:217396.2:2000SEP08
1127
1189
forward 2
TM
N out


46
LG:090574.1:2000SEP08
49
108
forward 1
TM
N out


47
LG:202943.1:2000SEP08
590
658
forward 2
TM
N out


47
LG:202943.1:2000SEP08
842
928
forward 2
TM
N out


47
LG:202943.1:2000SEP08
552
638
forward 3
TM
N out


48
LG:236928.1:2000SEP08
349
435
forward 1
TM
N in


48
LG:236928.1:2000SEP08
448
519
forward 1
TM
N in


48
LG:236928.1:2000SEP08
592
642
forward 1
TM
N in


48
LG:236928.1:2000SEP08
706
768
forward 1
TM
N in


48
LG:236928.1:2000SEP08
778
840
forward 1
TM
N in


48
LG:236928.1:2000SEP08
967
1038
forward 1
TM
N in


48
LG:236928.1:2000SEP08
1318
1374
forward 1
TM
N in


48
LG:236928.1:2000SEP08
1609
1695
forward 1
TM
N in


48
LG:236928.1:2000SEP08
1933
2016
forward 1
TM
N in


48
LG:236928.1:2000SEP08
2161
2247
forward 1
TM
N in


48
LG:236928.1:2000SEP08
2419
2475
forward 1
TM
N in


48
LG:236928.1:2000SEP08
2818
2865
forward 1
TM
N in


48
LG:236928.1:2000SEP08
2884
2946
forward 1
TM
N in


48
LG:236928.1:2000SEP08
2980
3042
forward 1
TM
N in


48
LG:236928.1:2000SEP08
3076
3138
forward 1
TM
N in


48
LG:236928.1:2000SEP08
335
421
forward 2
TM
N in


48
LG:236928.1:2000SEP08
437
499
forward 2
TM
N in


48
LG:236928.1:2000SEP08
524
586
forward 2
TM
N in


48
LG:236928.1:2000SEP08
659
718
forward 2
TM
N in


48
LG:236928.1:2000SEP08
1268
1351
forward 2
TM
N in


48
LG:236928.1:2000SEP08
1400
1471
forward 2
TM
N in


48
LG:236928.1:2000SEP08
1472
1534
forward 2
TM
N in


48
LG:236928.1:2000SEP08
1586
1669
forward 2
TM
N in


48
LG:236928.1:2000SEP08
1745
1831
forward 2
TM
N in


48
LG:236928.1:2000SEP08
1877
1963
forward 2
TM
N in


48
LG:236928.1:2000SEP08
2015
2101
forward 2
TM
N in


48
LG:236928.1:2000SEP08
2501
2587
forward 2
TM
N in


48
LG:236928.1:2000SEP08
2639
2716
forward 2
TM
N in


48
LG:236928.1:2000SEP08
2786
2872
forward 2
TM
N in


48
LG:236928.1:2000SEP08
2894
2980
forward 2
TM
N in


48
LG:236928.1:2000SEP08
471
551
forward 3
TM
N in


48
LG:236928.1:2000SEP08
738
824
forward 3
TM
N in


48
LG:236928.1:2000SEP08
1287
1340
forward 3
TM
N in


48
LG:236928.1:2000SEP08
1626
1712
forward 3
TM
N in


48
LG:236928.1:2000SEP08
1890
1976
forward 3
TM
N in


48
LG:236928.1:2000SEP08
2034
2120
forward 3
TM
N in


48
LG:236928.1:2000SEP08
2118
2186
forward 3
TM
N in


48
LG:236928.1:2000SEP08
2520
2591
forward 3
TM
N in


48
LG:236928.1:2000SEP08
2763
2846
forward 3
TM
N in


48
LG:236928.1:2000SEP08
2916
2978
forward 3
TM
N in


48
LG:236928.1:2000SEP08
3003
3065
forward 3
TM
N in


49
LG:215169.2:2000SEP08
1363
1413
forward 1
TM
N in


49
LG:215169.2:2000SEP08
503
589
forward 2
TM
N out


49
LG:215169.2:2000SEP08
1727
1813
forward 2
TM
N out


49
LG:215169.2:2000SEP08
237
302
forward 3
TM
N out


49
LG:215169.2:2000SEP08
837
923
forward 3
TM
N out


49
LG:215169.2:2000SEP08
1398
1460
forward 3
TM
N out


49
LG:215169.2:2000SEP08
1470
1532
forward 3
TM
N out


49
LG:215169.2:2000SEP08
1605
1658
forward 3
TM
N out


50
LG:410726.1:2000SEP08
31
93
forward 1
TM
N out


50
LG:410726.1:2000SEP08
115
177
forward 1
TM
N out


50
LG:410726.1:2000SEP08
463
549
forward 1
TM
N out


51
LG:234372.2:2000SEP08
325
411
forward 1
TM
N in


51
LG:234372.2:2000SEP08
2492
2578
forward 2
TM
N out


51
LG:234372.2:2000SEP08
2669
2743
forward 2
TM
N out


51
LG:234372.2:2000SEP08
723
809
forward 3
TM
N in


52
LG:022629.1:2000SEP08
268
354
forward 1
TM
N out


52
LG:022629.1:2000SEP08
385
459
forward 1
TM
N out


52
LG:022629.1:2000SEP08
559
645
forward 1
TM
N out


52
LG:022629.1:2000SEP08
796
882
forward 1
TM
N out


52
LG:022629.1:2000SEP08
281
358
forward 2
TM
N in


53
LG:068682.1:2000SEP08
707
793
forward 2
TM
N out


54
LG:222335.1:2000SEP08
847
933
forward 1
TM
N in


54
LG:222335.1:2000SEP08
973
1023
forward 1
TM
N in


54
LG:222335.1:2000SEP08
1030
1101
forward 1
TM
N in


54
LG:222335.1:2000SEP08
1216
1290
forward 1
TM
N in


54
LG:222335.1:2000SEP08
23
109
forward 2
TM


54
LG:222335.1:2000SEP08
314
373
forward 2
TM


54
LG:222335.1:2000SEP08
428
514
forward 2
TM


54
LG:222335.1:2000SEP08
728
784
forward 2
TM


54
LG:222335.1:2000SEP08
794
868
forward 2
TM


54
LG:222335.1:2000SEP08
965
1051
forward 2
TM


54
LG:222335.1:2000SEP08
603
674
forward 3
TM
N in


54
LG:222335.1:2000SEP08
921
983
forward 3
TM
N in


54
LG:222335.1:2000SEP08
1014
1076
forward 3
TM
N in


54
LG:222335.1:2000SEP08
1101
1187
forward 3
TM
N in


54
LG:222335.1:2000SEP08
1227
1277
forward 3
TM
N in


55
LG:331342.1:2000SEP08
22
96
forward 1
TM
N out


55
LG:331342.1:2000SEP08
289
339
forward 1
TM
N out


55
LG:331342.1:2000SEP08
645
731
forward 3
TM
N in


56
LG:021770.1:2000SEP08
286
372
forward 1
TM
N in


56
LG:021770.1:2000SEP08
400
477
forward 1
TM
N in


56
LG:021770.1:2000SEP08
502
579
forward 1
TM
N in


56
LG:021770.1:2000SEP08
784
852
forward 1
TM
N in


56
LG:021770.1:2000SEP08
1237
1323
forward 1
TM
N in


56
LG:021770.1:2000SEP08
2416
2499
forward 1
TM
N in


56
LG:021770.1:2000SEP08
2611
2697
forward 1
TM
N in


56
LG:021770.1:2000SEP08
1115
1201
forward 2
TM
N in


56
LG:021770.1:2000SEP08
1262
1336
forward 2
TM
N in


56
LG:021770.1:2000SEP08
2426
2509
forward 2
TM
N in


56
LG:021770.1:2000SEP08
2726
2776
forward 2
TM
N in


56
LG:021770.1:2000SEP08
534
614
forward 3
TM
N in


56
LG:021770.1:2000SEP08
1260
1346
forward 3
TM
N in


56
LG:021770.1:2000SEP08
1461
1547
forward 3
TM
N in


56
LG:021770.1:2000SEP08
1695
1778
forward 3
TM
N in


56
LG:021770.1:2000SEP08
2496
2576
forward 3
TM
N in


56
LG:021770.1:2000SEP08
2727
2792
forward 3
TM
N in


57
LG:181607.9:2000SEP08
439
525
forward 1
TM
N out


58
LG:1042768.1:2000SEP08
695
751
forward 2
TM
N out


58
LG:1042768.1:2000SEP08
93
143
forward 3
TM
N in


58
LG:1042768.1:2000SEP08
201
287
forward 3
TM
N in


58
LG:1042768.1:2000SEP08
351
437
forward 3
TM
N in


59
LG:282729.1:2000SEP08
256
309
forward 1
TM
N out


60
LG:998305.3:2000SEP08
429
488
forward 3
TM
N in


60
LG:998305.3:2000SEP08
705
770
forward 3
TM
N in


61
LG:1135213.1:2000SEP08
41
127
forward 2
TM
N out


61
LG:1135213.1:2000SEP08
215
274
forward 2
TM
N out


61
LG:1135213.1:2000SEP08
293
379
forward 2
TM
N out


61
LG:1135213.1:2000SEP08
389
475
forward 2
TM
N out


62
LG:267762.1:2000SEP08
854
937
forward 2
TM
N in


62
LG:267762.1:2000SEP08
1283
1345
forward 2
TM
N in


62
LG:267762.1:2000SEP08
1445
1531
forward 2
TM
N in


62
LG:267762.1:2000SEP08
1383
1469
forward 3
TM
N out


63
LG:120744.1:2000SEP08
181
249
forward 1
TM
N out


63
LG:120744.1:2000SEP08
188
256
forward 2
TM


63
LG:120744.1:2000SEP08
275
328
forward 2
TM


64
LG:403409.1:2000SEP08
136
222
forward 1
TM
N out


64
LG:403409.1:2000SEP08
973
1029
forward 1
TM
N out


64
LG:403409.1:2000SEP08
1285
1371
forward 1
TM
N out


64
LG:403409.1:2000SEP08
182
268
forward 2
TM
N in


65
LG:226874.3:2000SEP08
231
278
forward 3
TM
N out


66
LG:1045521.4:2000SEP08
1216
1266
forward 1
TM
N in


66
LG:1045521.4:2000SEP08
1567
1653
forward 1
TM
N in


66
LG:1045521.4:2000SEP08
1699
1761
forward 1
TM
N in


66
LG:1045521.4:2000SEP08
3091
3177
forward 1
TM
N in


66
LG:1045521.4:2000SEP08
3508
3582
forward 1
TM
N in


66
LG:1045521.4:2000SEP08
1652
1714
forward 2
TM
N in


66
LG:1045521.4:2000SEP08
2444
2500
forward 2
TM
N in


66
LG:1045521.4:2000SEP08
2627
2713
forward 2
TM
N in


66
LG:1045521.4:2000SEP08
3017
3088
forward 2
TM
N in


66
LG:1045521.4:2000SEP08
3317
3385
forward 2
TM
N in


66
LG:1045521.4:2000SEP08
1530
1604
forward 3
TM
N in


66
LG:1045521.4:2000SEP08
2496
2549
forward 3
TM
N in


66
LG:1045521.4:2000SEP08
2931
3017
forward 3
TM
N in


66
LG:1045521.4:2000SEP08
3267
3341
forward 3
TM
N in


67
LG:275876.1:2000SEP08
775
849
forward 1
TM
N in


67
LG:275876.1:2000SEP08
949
1002
forward 1
TM
N in


67
LG:275876.1:2000SEP08
842
928
forward 2
TM
N out


67
LG:275876.1:2000SEP08
777
842
forward 3
TM
N in


68
LG:475127.7:2000SEP08
137
223
forward 2
TM
N in


69
LG:157263.1:2000SEP08
175
249
forward 1
TM
N in


69
LG:157263.1:2000SEP08
295
345
forward 1
TM
N in


69
LG:157263.1:2000SEP08
406
492
forward 1
TM
N in


69
LG:157263.1:2000SEP08
793
867
forward 1
TM
N in


69
LG:157263.1:2000SEP08
889
951
forward 1
TM
N in


69
LG:157263.1:2000SEP08
1081
1143
forward 1
TM
N in


69
LG:157263.1:2000SEP08
1168
1230
forward 1
TM
N in


69
LG:157263.1:2000SEP08
1255
1341
forward 1
TM
N in


69
LG:157263.1:2000SEP08
482
544
forward 2
TM
N out


69
LG:157263.1:2000SEP08
563
625
forward 2
TM
N out


69
LG:157263.1:2000SEP08
180
266
forward 3
TM
N out


70
LG:247382.7:2000SEP08
808
894
forward 1
TM


70
LG:247382.7:2000SEP08
650
709
forward 2
TM
N out


70
LG:247382.7:2000SEP08
1412
1495
forward 2
TM
N out


71
LG:197367.5:2000SEP08
454
510
forward 1
TM
N out


72
LG:218090.5:2000SEP08
85
156
forward 1
TM
N out


72
LG:218090.5:2000SEP08
417
494
forward 3
TM
N out


73
LG:216612.4:2000SEP08
1615
1701
forward 1
TM
N in


73
LG:216612.4:2000SEP08
1942
2007
forward 1
TM
N in


73
LG:216612.4:2000SEP08
2182
2268
forward 1
TM
N in


73
LG:216612.4:2000SEP08
2413
2487
forward 1
TM
N in


73
LG:216612.4:2000SEP08
1583
1660
forward 2
TM
N in


73
LG:216612.4:2000SEP08
2114
2176
forward 2
TM
N in


73
LG:216612.4:2000SEP08
2216
2278
forward 2
TM
N in


73
LG:216612.4:2000SEP08
2339
2425
forward 2
TM
N in


73
LG:216612.4:2000SEP08
2483
2542
forward 2
TM
N in


73
LG:216612.4:2000SEP08
120
206
forward 3
TM
N in


73
LG:216612.4:2000SEP08
234
284
forward 3
TM
N in


73
LG:216612.4:2000SEP08
327
413
forward 3
TM
N in


73
LG:216612.4:2000SEP08
444
530
forward 3
TM
N in


73
LG:216612.4:2000SEP08
810
896
forward 3
TM
N in


73
LG:216612.4:2000SEP08
942
1028
forward 3
TM
N in


73
LG:216612.4:2000SEP08
1644
1730
forward 3
TM
N in


73
LG:216612.4:2000SEP08
1950
2012
forward 3
TM
N in


73
LG:216612.4:2000SEP08
2037
2099
forward 3
TM
N in


73
LG:216612.4:2000SEP08
2292
2378
forward 3
TM
N in


73
LG:216612.4:2000SEP08
2529
2615
forward 3
TM
N in


74
LG:197614.1:2000SEP08
484
537
forward 1
TM
N in


74
LG:197614.1:2000SEP08
2308
2367
forward 1
TM
N in


74
LG:197614.1:2000SEP08
3175
3246
forward 1
TM
N in


74
LG:197614.1:2000SEP08
3298
3354
forward 1
TM
N in


74
LG:197614.1:2000SEP08
3556
3612
forward 1
TM
N in


74
LG:197614.1:2000SEP08
3739
3825
forward 1
TM
N in


74
LG:197614.1:2000SEP08
3964
4050
forward 1
TM
N in


74
LG:197614.1:2000SEP08
4063
4134
forward 1
TM
N in


74
LG:197614.1:2000SEP08
4147
4215
forward 1
TM
N in


74
LG:197614.1:2000SEP08
374
460
forward 2
TM
N out


74
LG:197614.1:2000SEP08
800
862
forward 2
TM
N out


74
LG:197614.1:2000SEP08
875
937
forward 2
TM
N out


74
LG:197614.1:2000SEP08
1352
1414
forward 2
TM
N out


74
LG:197614.1:2000SEP08
1436
1498
forward 2
TM
N out


74
LG:197614.1:2000SEP08
2312
2398
forward 2
TM
N out


74
LG:197614.1:2000SEP08
3422
3469
forward 2
TM
N out


74
LG:197614.1:2000SEP08
3632
3718
forward 2
TM
N out


74
LG:197614.1:2000SEP08
3773
3835
forward 2
TM
N out


74
LG:197614.1:2000SEP08
3932
4003
forward 2
TM
N out


74
LG:197614.1:2000SEP08
4040
4126
forward 2
TM
N out


74
LG:197614.1:2000SEP08
4244
4312
forward 2
TM
N out


74
LG:197614.1:2000SEP08
4448
4504
forward 2
TM
N out


74
LG:197614.1:2000SEP08
489
575
forward 3
TM


74
LG:197614.1:2000SEP08
2967
3017
forward 3
TM


74
LG:197614.1:2000SEP08
3663
3749
forward 3
TM


74
LG:197614.1:2000SEP08
3912
3974
forward 3
TM


74
LG:197614.1:2000SEP08
4020
4082
forward 3
TM


74
LG:197614.1:2000SEP08
4341
4427
forward 3
TM


75
LG:378428.1:2000SEP08
703
789
forward 1
TM
N in


75
LG:378428.1:2000SEP08
1336
1422
forward 1
TM
N in


75
LG:378428.1:2000SEP08
1924
2010
forward 1
TM
N in


75
LG:378428.1:2000SEP08
2188
2268
forward 1
TM
N in


75
LG:378428.1:2000SEP08
2171
2224
forward 2
TM
N in


75
LG:378428.1:2000SEP08
1527
1577
forward 3
TM
N out


75
LG:378428.1:2000SEP08
1665
1751
forward 3
TM
N out


75
LG:378428.1:2000SEP08
1968
2054
forward 3
TM
N out


75
LG:378428.1:2000SEP08
2205
2291
forward 3
TM
N out


76
LG:286639.1:2000SEP08
127
213
forward 1
TM


76
LG:286639.1:2000SEP08
970
1032
forward 1
TM


76
LG:286639.1:2000SEP08
1066
1128
forward 1
TM


76
LG:286639.1:2000SEP08
1588
1662
forward 1
TM


76
LG:286639.1:2000SEP08
1786
1872
forward 1
TM


76
LG:286639.1:2000SEP08
62
148
forward 2
TM
N in


76
LG:286639.1:2000SEP08
1772
1825
forward 2
TM
N in


76
LG:286639.1:2000SEP08
267
320
forward 3
TM
N out


76
LG:286639.1:2000SEP08
999
1085
forward 3
TM
N out


76
LG:286639.1:2000SEP08
1902
1967
forward 3
TM
N out


77
LG:389870.1:2000SEP08
1066
1113
forward 1
TM
N out


77
LG:389870.1:2000SEP08
1055
1120
forward 2
TM
N in


77
LG:389870.1:2000SEP08
1059
1142
forward 3
TM
N in


78
LG:1387485.6:2000SEP08
1213
1275
forward 1
TM
N in


78
LG:1387485.6:2000SEP08
206
292
forward 2
TM
N in


78
LG:1387485.6:2000SEP08
824
886
forward 2
TM
N in


78
LG:1387485.6:2000SEP08
914
976
forward 2
TM
N in


78
LG:1387485.6:2000SEP08
1244
1321
forward 2
TM
N in


78
LG:1387485.6:2000SEP08
396
473
forward 3
TM
N out


78
LG:1387485.6:2000SEP08
537
602
forward 3
TM
N out


78
LG:1387485.6:2000SEP08
660
746
forward 3
TM
N out


78
LG:1387485.6:2000SEP08
786
872
forward 3
TM
N out


78
LG:1387485.6:2000SEP08
1164
1226
forward 3
TM
N out


78
LG:1387485.6:2000SEP08
1245
1307
forward 3
TM
N out


79
LG:230151.1:2000SEP08
1774
1860
forward 1
TM
N in


79
LG:230151.1:2000SEP08
1091
1165
forward 2
TM
N out


79
LG:230151.1:2000SEP08
1193
1246
forward 2
TM
N out


79
LG:230151.1:2000SEP08
1757
1843
forward 2
TM
N out


80
LG:215158.5:2000SEP08
199
267
forward 1
TM
N out


80
LG:215158.5:2000SEP08
820
873
forward 1
TM
N out


80
LG:215158.5:2000SEP08
892
945
forward 1
TM
N out


80
LG:215158.5:2000SEP08
908
985
forward 2
TM
N out


80
LG:215158.5:2000SEP08
1433
1504
forward 2
TM
N out


80
LG:215158.5:2000SEP08
447
533
forward 3
TM


81
LG:235840.1:2000SEP08
265
342
forward 1
TM
N out


81
LG:235840.1:2000SEP08
511
579
forward 1
TM
N out


81
LG:235840.1:2000SEP08
577
639
forward 1
TM
N out


81
LG:235840.1:2000SEP08
730
786
forward 1
TM
N out


81
LG:235840.1:2000SEP08
2011
2082
forward 1
TM
N out


81
LG:235840.1:2000SEP08
2110
2172
forward 1
TM
N out


81
LG:235840.1:2000SEP08
2326
2406
forward 1
TM
N out


81
LG:235840.1:2000SEP08
2416
2502
forward 1
TM
N out


81
LG:235840.1:2000SEP08
116
178
forward 2
TM
N out


81
LG:235840.1:2000SEP08
191
253
forward 2
TM
N out


81
LG:235840.1:2000SEP08
500
586
forward 2
TM
N out


81
LG:235840.1:2000SEP08
731
817
forward 2
TM
N out


81
LG:235840.1:2000SEP08
848
916
forward 2
TM
N out


81
LG:235840.1:2000SEP08
956
1030
forward 2
TM
N out


81
LG:235840.1:2000SEP08
1973
2050
forward 2
TM
N out


81
LG:235840.1:2000SEP08
192
278
forward 3
TM
N out


81
LG:235840.1:2000SEP08
516
590
forward 3
TM
N out


81
LG:235840.1:2000SEP08
711
797
forward 3
TM
N out


81
LG:235840.1:2000SEP08
819
905
forward 3
TM
N out


81
LG:235840.1:2000SEP08
1446
1529
forward 3
TM
N out


81
LG:235840.1:2000SEP08
1893
1976
forward 3
TM
N out


81
LG:235840.1:2000SEP08
2298
2360
forward 3
TM
N out


82
LG:350272.1:2000SEP08
1675
1746
forward 1
TM
N in


82
LG:350272.1:2000SEP08
2374
2436
forward 1
TM
N in


82
LG:350272.1:2000SEP08
104
190
forward 2
TM
N in


82
LG:350272.1:2000SEP08
2264
2332
forward 2
TM
N in


82
LG:350272.1:2000SEP08
2369
2440
forward 2
TM
N in


82
LG:350272.1:2000SEP08
12
95
forward 3
TM
N in


82
LG:350272.1:2000SEP08
993
1052
forward 3
TM
N in


82
LG:350272.1:2000SEP08
2067
2138
forward 3
TM
N in


82
LG:350272.1:2000SEP08
2334
2399
forward 3
TM
N in


83
LG:232190.1:2000SEP08
592
678
forward 1
TM
N in


83
LG:232190.1:2000SEP08
1423
1500
forward 1
TM
N in


83
LG:232190.1:2000SEP08
158
241
forward 2
TM
N in


83
LG:232190.1:2000SEP08
293
373
forward 2
TM
N in


83
LG:232190.1:2000SEP08
644
730
forward 2
TM
N in


83
LG:232190.1:2000SEP08
761
847
forward 2
TM
N in


83
LG:232190.1:2000SEP08
1466
1552
forward 2
TM
N in


83
LG:232190.1:2000SEP08
279
356
forward 3
TM
N in


83
LG:232190.1:2000SEP08
588
674
forward 3
TM
N in


83
LG:232190.1:2000SEP08
936
1022
forward 3
TM
N in


84
LG:1068127.1:2000SEP08
423
470
forward 3
TM


85
LG:408751.3:2000SEP08
2194
2253
forward 1
TM
N out


85
LG:408751.3:2000SEP08
2320
2406
forward 1
TM
N out


85
LG:408751.3:2000SEP08
1907
1993
forward 2
TM
N out


85
LG:408751.3:2000SEP08
2378
2464
forward 2
TM
N out


85
LG:408751.3:2000SEP08
1866
1928
forward 3
TM
N in


85
LG:408751.3:2000SEP08
2328
2414
forward 3
TM
N in


86
LG:1078933.1:2000SEP08
905
991
forward 2
TM
N in


86
LG:1078933.1:2000SEP08
924
1010
forward 3
TM
N in


87
LG:958731.1:2000SEP08
15
101
forward 3
TM
N out


88
LG:024125.5:2000SEP08
474
554
forward 3
TM


89
LG:373637.3:2000SEP08
473
559
forward 2
TM
N in


89
LG:373637.3:2000SEP08
854
934
forward 2
TM
N in


90
LG:1053229.1:2000SEP08
410
487
forward 2
TM
N out


91
LG:248364.1:2000SEP08
439
495
forward 1
TM
N out


92
LG:477130.1:2000SEP08
37
108
forward 1
TM
N in


92
LG:477130.1:2000SEP08
406
489
forward 1
TM
N in


92
LG:477130.1:2000SEP08
685
759
forward 1
TM
N in


92
LG:477130.1:2000SEP08
641
727
forward 2
TM
N in


92
LG:477130.1:2000SEP08
741
827
forward 3
TM
N in


93
LG:113786.17:2000SEP08
89
139
forward 2
TM
N out


93
LG:113786.17:2000SEP08
18
68
forward 3
TM


94
LG:347635.1:2000SEP08
220
294
forward 1
TM
N out


94
LG:347635.1:2000SEP08
406
456
forward 1
TM
N out


94
LG:347635.1:2000SEP08
479
550
forward 2
TM
N out


94
LG:347635.1:2000SEP08
1283
1369
forward 2
TM
N out


94
LG:347635.1:2000SEP08
615
701
forward 3
TM
N out


94
LG:347635.1:2000SEP08
1347
1397
forward 3
TM
N out


95
LG:242966.4:2000SEP08
1439
1510
forward 2
TM
N in


96
LG:217814.1:2000SEP08
1621
1689
forward 1
TM
N out


96
LG:217814.1:2000SEP08
1622
1708
forward 2
TM
N out


96
LG:217814.1:2000SEP08
246
302
forward 3
TM
N in


96
LG:217814.1:2000SEP08
1695
1772
forward 3
TM
N in


97
LG:476452.1:2000SEP08
556
624
forward 1
TM
N out


97
LG:476452.1:2000SEP08
988
1074
forward 1
TM
N out


98
LG:1100657.1:2000SEP08
31
117
forward 1
TM
N out


99
LG:1132418.2:2000SEP08
43
129
forward 1
TM
N out


99
LG:1132418.2:2000SEP08
244
327
forward 1
TM
N out


100
LG:1098570.1:2000SEP08
400
453
forward 1
TM
N out


100
LG:1098570.1:2000SEP08
26
85
forward 2
TM
N out


101
LG:1097987.1:2000SEP08
152
208
forward 2
TM
N out


101
LG:1097987.1:2000SEP08
141
215
forward 3
TM


101
LG:1097987.1:2000SEP08
912
971
forward 3
TM


102
LG:337818.2:2000SEP08
40
117
forward 1
TM
N out


102
LG:337818.2:2000SEP08
532
618
forward 1
TM
N out


102
LG:337818.2:2000SEP08
907
993
forward 1
TM
N out


102
LG:337818.2:2000SEP08
1360
1425
forward 1
TM
N out


103
LG:1040582.1:2000SEP08
31
117
forward 1
TM
N in


103
LG:1040582.1:2000SEP08
539
595
forward 2
TM
N out


103
LG:1040582.1:2000SEP08
330
416
forward 3
TM
N out


104
LG:1099122.1:2000SEP08
385
456
forward 1
TM
N out


104
LG:1099122.1:2000SEP08
236
292
forward 2
TM
N in


104
LG:1099122.1:2000SEP08
350
436
forward 2
TM
N in


104
LG:1099122.1:2000SEP08
258
308
forward 3
TM
N out


104
LG:1099122.1:2000SEP08
420
470
forward 3
TM
N out


105
LG:1327449.1:2000SEP08
112
198
forward 1
TM
N out


105
LG:1327449.1:2000SEP08
268
318
forward 1
TM
N out


105
LG:1327449.1:2000SEP08
395
481
forward 2
TM
N out


106
LG:227933.5:2000SEP08
1114
1200
forward 1
TM
N in


106
LG:227933.5:2000SEP08
1231
1290
forward 1
TM
N in


106
LG:227933.5:2000SEP08
255
308
forward 3
TM
N out


107
LG:1043709.2:2000SEP08
600
650
forward 3
TM
N out


108
LG:1099871.1:2000SEP08
181
243
forward 1
TM
N out


109
LG:1399139.4:2000SEP08
289
369
forward 1
TM
N out


109
LG:1399139.4:2000SEP08
616
684
forward 1
TM
N out


109
LG:1399139.4:2000SEP08
185
235
forward 2
TM


109
LG:1399139.4:2000SEP08
555
641
forward 3
TM
N out


110
LG:236386.1:2000SEP08
106
171
forward 1
TM
N out


110
LG:236386.1:2000SEP08
271
357
forward 1
TM
N out


110
LG:236386.1:2000SEP08
3097
3159
forward 1
TM
N out


110
LG:236386.1:2000SEP08
3715
3789
forward 1
TM
N out


110
LG:236386.1:2000SEP08
3093
3164
forward 3
TM
N out


110
LG:236386.1:2000SEP08
3759
3812
forward 3
TM
N out


111
LG:1015157.1:2000SEP08
320
406
forward 2
TM
N in


112
LG:1065433.1:2000SEP08
790
876
forward 1
TM
N in


113
LG:236992.4:2000SEP08
421
471
forward 1
TM
N out


113
LG:236992.4:2000SEP08
14
100
forward 2
TM
N out


114
LG:1071124.1:2000SEP08
171
257
forward 3
TM
N out


115
LG:206425.2:2000SEP08
175
237
forward 1
TM
N in


115
LG:206425.2:2000SEP08
424
483
forward 1
TM
N in


115
LG:206425.2:2000SEP08
1810
1896
forward 1
TM
N in


115
LG:206425.2:2000SEP08
1939
2001
forward 1
TM
N in


115
LG:206425.2:2000SEP08
404
457
forward 2
TM
N in


115
LG:206425.2:2000SEP08
2168
2254
forward 2
TM
N in


115
LG:206425.2:2000SEP08
561
620
forward 3
TM
N out


115
LG:206425.2:2000SEP08
1908
1994
forward 3
TM
N out


116
LG:885747.2:2000SEP08
125
205
forward 2
TM
N in


116
LG:885747.2:2000SEP08
135
191
forward 3
TM
N out


116
LG:885747.2:2000SEP08
189
239
forward 3
TM
N out


117
LG:1140501.1:2000SEP08
622
708
forward 1
TM
N out


117
LG:1140501.1:2000SEP08
844
918
forward 1
TM
N out


117
LG:1140501.1:2000SEP08
1138
1206
forward 1
TM
N out


117
LG:1140501.1:2000SEP08
86
169
forward 2
TM
N out


117
LG:1140501.1:2000SEP08
221
301
forward 2
TM
N out


117
LG:1140501.1:2000SEP08
617
703
forward 2
TM
N out


117
LG:1140501.1:2000SEP08
606
677
forward 3
TM
N in


118
LG:001239.1:2000SEP08
1048
1122
forward 1
TM
N out


118
LG:001239.1:2000SEP08
669
755
forward 3
TM
N out


118
LG:001239.1:2000SEP08
1911
1976
forward 3
TM
N out


119
LG:018980.1:2000SEP08
124
204
forward 1
TM
N out


119
LG:018980.1:2000SEP08
944
997
forward 2
TM
N out


119
LG:018980.1:2000SEP08
405
464
forward 3
TM
N out


119
LG:018980.1:2000SEP08
900
986
forward 3
TM
N out


119
LG:018980.1:2000SEP08
1017
1103
forward 3
TM
N out


120
LG:1083120.3:2000SEP08
214
291
forward 1
TM
N out


120
LG:1083120.3:2000SEP08
233
319
forward 2
TM
N out


120
LG:1083120.3:2000SEP08
252
320
forward 3
TM
N in


121
LG:233258.3:2000SEP08
58
141
forward 1
TM


121
LG:233258.3:2000SEP08
1783
1842
forward 1
TM


121
LG:233258.3:2000SEP08
2248
2322
forward 1
TM


121
LG:233258.3:2000SEP08
4522
4596
forward 1
TM


121
LG:233258.3:2000SEP08
4208
4294
forward 2
TM
N out


121
LG:233258.3:2000SEP08
4478
4534
forward 2
TM
N out


121
LG:233258.3:2000SEP08
390
476
forward 3
TM
N in


121
LG:233258.3:2000SEP08
2766
2852
forward 3
TM
N in


122
LG:999062.1:2000SEP08
455
508
forward 2
TM
N in


122
LG:999062.1:2000SEP08
510
596
forward 3
TM
N in


123
LG:887776.1:2000SEP08
14
91
forward 2
TM
N out


124
LG:1400301.2:2000SEP08
445
531
forward 1
TM
N out


124
LG:1400301.2:2000SEP08
456
518
forward 3
TM
N out


125
LG:1329362.1:2000SEP08
18
104
forward 3
TM
N out


126
LG:1096498.1:2000SEP08
137
199
forward 2
TM
N out


126
LG:1096498.1:2000SEP08
201
269
forward 3
TM
N out


126
LG:1096498.1:2000SEP08
321
371
forward 3
TM
N out


127
LG:1096337.1:2000SEP08
625
711
forward 1
TM
N out


127
LG:1096337.1:2000SEP08
500
553
forward 2
TM


128
LG:1400579.1:2000SEP08
797
883
forward 2
TM
N out


128
LG:1400579.1:2000SEP08
9
86
forward 3
TM
N out


128
LG:1400579.1:2000SEP08
669
755
forward 3
TM
N out


129
LG:1080091.1:2000SEP08
67
114
forward 1
TM
N out


129
LG:1080091.1:2000SEP08
435
497
forward 3
TM
N out


130
LG:1082203.1:2000SEP08
1438
1521
forward 1
TM
N in


130
LG:1082203.1:2000SEP08
155
217
forward 2
TM
N out


130
LG:1082203.1:2000SEP08
272
358
forward 2
TM
N out


131
LG:1084051.1:2000SEP08
301
366
forward 1
TM
N out


131
LG:1084051.1:2000SEP08
934
1017
forward 1
TM
N out


131
LG:1084051.1:2000SEP08
1072
1140
forward 1
TM
N out


131
LG:1084051.1:2000SEP08
875
961
forward 2
TM
N out


131
LG:1084051.1:2000SEP08
882
968
forward 3
TM
N in


131
LG:1084051.1:2000SEP08
1071
1151
forward 3
TM
N in


132
LG:1082393.1:2000SEP08
505
579
forward 1
TM
N in


132
LG:1082393.1:2000SEP08
1710
1784
forward 3
TM
N in


133
LG:1086183.1:2000SEP08
1093
1179
forward 1
TM
N out


133
LG:1086183.1:2000SEP08
1166
1252
forward 2
TM
N in


133
LG:1086183.1:2000SEP08
15
86
forward 3
TM


133
LG:1086183.1:2000SEP08
381
437
forward 3
TM


133
LG:1086183.1:2000SEP08
1194
1280
forward 3
TM


134
LG:1090268.1:2000SEP08
1882
1953
forward 1
TM
N out


134
LG:1090268.1:2000SEP08
1969
2055
forward 1
TM
N out


134
LG:1090268.1:2000SEP08
1670
1729
forward 2
TM
N out


134
LG:1090268.1:2000SEP08
1853
1939
forward 2
TM
N out


134
LG:1090268.1:2000SEP08
1997
2083
forward 2
TM
N out


134
LG:1090268.1:2000SEP08
1485
1550
forward 3
TM
N in


134
LG:1090268.1:2000SEP08
1869
1943
forward 3
TM
N in


134
LG:1090268.1:2000SEP08
1962
2048
forward 3
TM
N in


135
LG:1400597.5:2000SEP08
134
199
forward 2
TM
N in


136
LG:1080307.2:2000SEP08
275
346
forward 2
TM
N out


136
LG:1080307.2:2000SEP08
347
403
forward 2
TM
N out


136
LG:1080307.2:2000SEP08
183
269
forward 3
TM
N in


136
LG:1080307.2:2000SEP08
303
371
forward 3
TM
N in


137
LG:1400603.2:2000SEP08
792
878
forward 3
TM
N in


137
LG:1400603.2:2000SEP08
903
971
forward 3
TM
N in


137
LG:1400603.2:2000SEP08
1068
1151
forward 3
TM
N in


138
LG:1052984.1:2000SEP08
496
582
forward 1
TM
N in


138
LG:1052984.1:2000SEP08
509
595
forward 2
TM
N out


138
LG:1052984.1:2000SEP08
495
581
forward 3
TM


139
LG:1091259.1:2000SEP08
799
885
forward 1
TM
N in


140
LG:1082263.2:2000SEP08
1390
1458
forward 1
TM
N in


140
LG:1082263.2:2000SEP08
1558
1644
forward 1
TM
N in


140
LG:1082263.2:2000SEP08
83
169
forward 2
TM


140
LG:1082263.2:2000SEP08
1526
1612
forward 2
TM


140
LG:1082263.2:2000SEP08
1578
1664
forward 3
TM
N in


141
LG:1048604.2:2000SEP08
562
618
forward 1
TM
N in


141
LG:1048604.2:2000SEP08
697
768
forward 1
TM
N in


141
LG:1048604.2:2000SEP08
856
930
forward 1
TM
N in


141
LG:1048604.2:2000SEP08
332
418
forward 2
TM
N in


141
LG:1048604.2:2000SEP08
689
775
forward 2
TM
N in


141
LG:1048604.2:2000SEP08
1115
1192
forward 2
TM
N in


141
LG:1048604.2:2000SEP08
483
557
forward 3
TM
N in


141
LG:1048604.2:2000SEP08
570
638
forward 3
TM
N in


141
LG:1048604.2:2000SEP08
678
743
forward 3
TM
N in


141
LG:1048604.2:2000SEP08
1113
1199
forward 3
TM
N in


142
LG:1085254.3:2000SEP08
331
378
forward 1
TM
N in


142
LG:1085254.3:2000SEP08
204
290
forward 3
TM
N out


143
LG:1400606.2:2000SEP08
1096
1176
forward 1
TM
N out


143
LG:1400606.2:2000SEP08
794
880
forward 2
TM
N in


143
LG:1400606.2:2000SEP08
1031
1117
forward 2
TM
N in


143
LG:1400606.2:2000SEP08
93
173
forward 3
TM
N in


143
LG:1400606.2:2000SEP08
765
851
forward 3
TM
N in


144
LG:1090358.2:2000SEP08
250
336
forward 1
TM
N in


144
LG:1090358.2:2000SEP08
758
844
forward 2
TM
N out


144
LG:1090358.2:2000SEP08
848
919
forward 2
TM
N out


144
LG:1090358.2:2000SEP08
974
1060
forward 2
TM
N out


145
LG:1079064.2:2000SEP08
862
936
forward 1
TM
N out


146
LG:1076866.1:2000SEP08
2113
2187
forward 1
TM
N in


146
LG:1076866.1:2000SEP08
2111
2170
forward 2
TM


146
LG:1076866.1:2000SEP08
501
587
forward 3
TM
N in


146
LG:1076866.1:2000SEP08
2148
2234
forward 3
TM
N in


147
LG:969359.1:2000SEP08
256
303
forward 1
TM
N out


147
LG:969359.1:2000SEP08
276
350
forward 3
TM
N out


148
LG:366783.1:2000SEP08
1060
1143
forward 1
TM
N in


148
LG:366783.1:2000SEP08
470
550
forward 2
TM


148
LG:366783.1:2000SEP08
1050
1109
forward 3
TM
N in


149
LG:332176.3:2000SEP08
442
495
forward 1
TM
N in


149
LG:332176.3:2000SEP08
209
295
forward 2
TM
N in


149
LG:332176.3:2000SEP08
234
299
forward 3
TM
N in


149
LG:332176.3:2000SEP08
792
851
forward 3
TM
N in


149
LG:332176.3:2000SEP08
876
938
forward 3
TM
N in


149
LG:332176.3:2000SEP08
966
1028
forward 3
TM
N in


150
LG:994938.1:2000SEP08
562
618
forward 1
TM
N out


150
LG:994938.1:2000SEP08
287
343
forward 2
TM
N out


150
LG:994938.1:2000SEP08
512
598
forward 2
TM
N out


150
LG:994938.1:2000SEP08
279
356
forward 3
TM
N out


150
LG:994938.1:2000SEP08
474
557
forward 3
TM
N out


151
LG:982800.1:2000SEP08
25
81
forward 1
TM
N out


151
LG:982800.1:2000SEP08
1708
1782
forward 1
TM
N out


151
LG:982800.1:2000SEP08
2305
2391
forward 1
TM
N out


151
LG:982800.1:2000SEP08
1658
1744
forward 2
TM
N in


151
LG:982800.1:2000SEP08
1880
1927
forward 2
TM
N in


151
LG:982800.1:2000SEP08
2255
2341
forward 2
TM
N in


151
LG:982800.1:2000SEP08
1614
1697
forward 3
TM
N in


151
LG:982800.1:2000SEP08
2220
2306
forward 3
TM
N in


152
LG:977850.7:2000SEP08
58
144
forward 1
TM
N out


152
LG:977850.7:2000SEP08
187
237
forward 1
TM
N out


152
LG:977850.7:2000SEP08
35
112
forward 2
TM
N out


152
LG:977850.7:2000SEP08
48
116
forward 3
TM
N in


153
LG:234748.2:2000SEP08
25
99
forward 1
TM
N out


153
LG:234748.2:2000SEP08
601
663
forward 1
TM
N out


153
LG:234748.2:2000SEP08
679
741
forward 1
TM
N out


153
LG:234748.2:2000SEP08
871
957
forward 1
TM
N out


153
LG:234748.2:2000SEP08
1162
1230
forward 1
TM
N out


153
LG:234748.2:2000SEP08
1237
1302
forward 1
TM
N out


153
LG:234748.2:2000SEP08
1579
1641
forward 1
TM
N out


153
LG:234748.2:2000SEP08
1984
2070
forward 1
TM
N out


153
LG:234748.2:2000SEP08
2110
2196
forward 1
TM
N out


153
LG:234748.2:2000SEP08
2308
2355
forward 1
TM
N out


153
LG:234748.2:2000SEP08
359
421
forward 2
TM


153
LG:234748.2:2000SEP08
464
526
forward 2
TM


153
LG:234748.2:2000SEP08
656
742
forward 2
TM


153
LG:234748.2:2000SEP08
899
949
forward 2
TM


153
LG:234748.2:2000SEP08
995
1057
forward 2
TM


153
LG:234748.2:2000SEP08
1076
1138
forward 2
TM


153
LG:234748.2:2000SEP08
1412
1489
forward 2
TM


153
LG:234748.2:2000SEP08
1925
1999
forward 2
TM


153
LG:234748.2:2000SEP08
2012
2071
forward 2
TM


153
LG:234748.2:2000SEP08
2105
2191
forward 2
TM


153
LG:234748.2:2000SEP08
2204
2290
forward 2
TM


153
LG:234748.2:2000SEP08
393
455
forward 3
TM
N in


153
LG:234748.2:2000SEP08
474
536
forward 3
TM
N in


153
LG:234748.2:2000SEP08
645
725
forward 3
TM
N in


153
LG:234748.2:2000SEP08
801
863
forward 3
TM
N in


153
LG:234748.2:2000SEP08
894
956
forward 3
TM
N in


153
LG:234748.2:2000SEP08
1485
1535
forward 3
TM
N in


153
LG:234748.2:2000SEP08
2052
2114
forward 3
TM
N in


153
LG:234748.2:2000SEP08
2145
2207
forward 3
TM
N in


153
LG:234748.2:2000SEP08
2238
2300
forward 3
TM
N in


154
LG:306284.1:2000SEP08
255
305
forward 3
TM
N in


177
LI:335923.2:2000SEP08
149
229
forward 2
TM
N in


178
LI:345884.1:2000SEP08
61
147
forward 1
TM
N out


179
LI:417127.1:2000SEP08
148
201
forward 1
TM
N in


179
LI:417127.1:2000SEP08
114
200
forward 3
TM
N in


180
LI:451710.1:2000SEP08
502
588
forward 1
TM
N in


180
LI:451710.1:2000SEP08
453
515
forward 3
TM
N in


181
LI:406882.2:2000SEP08
109
180
forward 1
TM
N in


181
LI:406882.2:2000SEP08
514
597
forward 1
TM
N in


181
LI:406882.2:2000SEP08
1045
1101
forward 1
TM
N in


181
LI:406882.2:2000SEP08
293
379
forward 2
TM
N out


181
LI:406882.2:2000SEP08
653
739
forward 2
TM
N out


181
LI:406882.2:2000SEP08
1091
1141
forward 2
TM
N out


181
LI:406882.2:2000SEP08
675
746
forward 3
TM
N out


182
LI:728223.1:2000SEP08
45
131
forward 3
TM
N out


182
LI:728223.1:2000SEP08
129
179
forward 3
TM
N out


183
LI:289783.19:2000SEP08
10
93
forward 1
TM
N in


183
LI:289783.19:2000SEP08
151
204
forward 1
TM
N in


183
LI:289783.19:2000SEP08
11
94
forward 2
TM


183
LI:289783.19:2000SEP08
140
226
forward 2
TM


183
LI:289783.19:2000SEP08
489
575
forward 3
TM
N in


184
LI:235255.8:2000SEP08
985
1044
forward 1
TM
N out


185
LI:237693.5:2000SEP08
355
429
forward 1
TM
N in


186
LI:433670.3:2000SEP08
79
165
forward 1
TM


186
LI:433670.3:2000SEP08
598
681
forward 1
TM


186
LI:433670.3:2000SEP08
796
867
forward 1
TM


186
LI:433670.3:2000SEP08
74
160
forward 2
TM
N in


186
LI:433670.3:2000SEP08
221
292
forward 2
TM
N in


186
LI:433670.3:2000SEP08
662
736
forward 2
TM
N in


186
LI:433670.3:2000SEP08
848
898
forward 2
TM
N in


186
LI:433670.3:2000SEP08
75
161
forward 3
TM
N in


186
LI:433670.3:2000SEP08
387
449
forward 3
TM
N in


186
LI:433670.3:2000SEP08
651
737
forward 3
TM
N in


187
LI:202943.4:2000SEP08
535
609
forward 1
TM
N out


187
LI:202943.4:2000SEP08
1570
1656
forward 1
TM
N out


187
LI:202943.4:2000SEP08
342
395
forward 3
TM
N out


187
LI:202943.4:2000SEP08
495
557
forward 3
TM
N out


187
LI:202943.4:2000SEP08
579
641
forward 3
TM
N out


187
LI:202943.4:2000SEP08
759
845
forward 3
TM
N out


187
LI:202943.4:2000SEP08
1653
1721
forward 3
TM
N out


187
LI:202943.4:2000SEP08
1905
1991
forward 3
TM
N out


188
LI:068682.1:2000SEP08
700
786
forward 1
TM
N out


189
LI:203301.3:2000SEP08
643
729
forward 1
TM
N out


189
LI:203301.3:2000SEP08
1510
1572
forward 1
TM
N out


189
LI:203301.3:2000SEP08
1585
1647
forward 1
TM
N out


189
LI:203301.3:2000SEP08
1774
1842
forward 1
TM
N out


189
LI:203301.3:2000SEP08
2014
2100
forward 1
TM
N out


189
LI:203301.3:2000SEP08
2158
2220
forward 1
TM
N out


189
LI:203301.3:2000SEP08
2383
2469
forward 1
TM
N out


189
LI:203301.3:2000SEP08
2548
2634
forward 1
TM
N out


189
LI:203301.3:2000SEP08
2662
2724
forward 1
TM
N out


189
LI:203301.3:2000SEP08
2749
2835
forward 1
TM
N out


189
LI:203301.3:2000SEP08
1685
1771
forward 2
TM
N in


189
LI:203301.3:2000SEP08
2162
2233
forward 2
TM
N in


189
LI:203301.3:2000SEP08
2342
2428
forward 2
TM
N in


189
LI:203301.3:2000SEP08
2519
2572
forward 2
TM
N in


189
LI:203301.3:2000SEP08
2597
2674
forward 2
TM
N in


189
LI:203301.3:2000SEP08
117
170
forward 3
TM
N in


189
LI:203301.3:2000SEP08
387
470
forward 3
TM
N in


189
LI:203301.3:2000SEP08
1086
1136
forward 3
TM
N in


189
LI:203301.3:2000SEP08
1344
1430
forward 3
TM
N in


189
LI:203301.3:2000SEP08
1626
1712
forward 3
TM
N in


189
LI:203301.3:2000SEP08
2364
2435
forward 3
TM
N in


189
LI:203301.3:2000SEP08
2604
2672
forward 3
TM
N in


190
LI:020726.3:2000SEP08
1363
1449
forward 1
TM
N in


190
LI:020726.3:2000SEP08
1795
1863
forward 1
TM
N in


190
LI:020726.3:2000SEP08
1930
1992
forward 1
TM
N in


190
LI:020726.3:2000SEP08
545
631
forward 2
TM
N in


190
LI:020726.3:2000SEP08
656
742
forward 2
TM
N in


190
LI:020726.3:2000SEP08
767
829
forward 2
TM
N in


190
LI:020726.3:2000SEP08
839
901
forward 2
TM
N in


190
LI:020726.3:2000SEP08
938
1024
forward 2
TM
N in


190
LI:020726.3:2000SEP08
1391
1477
forward 2
TM
N in


190
LI:020726.3:2000SEP08
1598
1672
forward 2
TM
N in


190
LI:020726.3:2000SEP08
1790
1852
forward 2
TM
N in


190
LI:020726.3:2000SEP08
1874
1936
forward 2
TM
N in


190
LI:020726.3:2000SEP08
1958
2020
forward 2
TM
N in


191
LI:027209.1:2000SEP08
25
111
forward 1
TM
N out


191
LI:027209.1:2000SEP08
1129
1203
forward 1
TM
N out


191
LI:027209.1:2000SEP08
1219
1305
forward 1
TM
N out


191
LI:027209.1:2000SEP08
1447
1533
forward 1
TM
N out


191
LI:027209.1:2000SEP08
413
475
forward 2
TM
N out


191
LI:027209.1:2000SEP08
527
601
forward 2
TM
N out


191
LI:027209.1:2000SEP08
659
739
forward 2
TM
N out


191
LI:027209.1:2000SEP08
785
847
forward 2
TM
N out


191
LI:027209.1:2000SEP08
1178
1234
forward 2
TM
N out


191
LI:027209.1:2000SEP08
1232
1309
forward 2
TM
N out


191
LI:027209.1:2000SEP08
1379
1465
forward 2
TM
N out


191
LI:027209.1:2000SEP08
510
563
forward 3
TM
N in


191
LI:027209.1:2000SEP08
882
938
forward 3
TM
N in


191
LI:027209.1:2000SEP08
945
1016
forward 3
TM
N in


191
LI:027209.1:2000SEP08
1041
1112
forward 3
TM
N in


191
LI:027209.1:2000SEP08
1146
1208
forward 3
TM
N in


191
LI:027209.1:2000SEP08
1224
1286
forward 3
TM
N in


192
LI:108819.1:2000SEP08
196
264
forward 1
TM
N in


192
LI:108819.1:2000SEP08
203
271
forward 2
TM


192
LI:108819.1:2000SEP08
290
343
forward 2
TM


193
LI:021759.1:2000SEP08
133
186
forward 1
TM
N out


193
LI:021759.1:2000SEP08
59
115
forward 2
TM
N out


193
LI:021759.1:2000SEP08
495
581
forward 3
TM
N in


193
LI:021759.1:2000SEP08
981
1067
forward 3
TM
N in


194
LI:1165967.1:2000SEP08
323
403
forward 2
TM
N out


195
LI:1166315.1:2000SEP08
693
749
forward 3
TM
N out


196
LI:204626.1:2000SEP08
19
99
forward 1
TM
N out


197
LI:801140.1:2000SEP08
421
498
forward 1
TM
N in


198
LI:286639.1:2000SEP08
127
213
forward 1
TM
N out


198
LI:286639.1:2000SEP08
982
1068
forward 1
TM
N out


198
LI:286639.1:2000SEP08
1879
1944
forward 1
TM
N out


198
LI:286639.1:2000SEP08
62
148
forward 2
TM
N out


198
LI:286639.1:2000SEP08
965
1027
forward 2
TM
N out


198
LI:286639.1:2000SEP08
1061
1123
forward 2
TM
N out


198
LI:286639.1:2000SEP08
1589
1663
forward 2
TM
N out


198
LI:286639.1:2000SEP08
1787
1873
forward 2
TM
N out


198
LI:286639.1:2000SEP08
267
320
forward 3
TM
N out


198
LI:286639.1:2000SEP08
1794
1847
forward 3
TM
N out


199
LI:288905.4:2000SEP08
868
927
forward 1
TM
N out


199
LI:288905.4:2000SEP08
1552
1638
forward 1
TM
N out


199
LI:288905.4:2000SEP08
1913
1975
forward 2
TM
N out


199
LI:288905.4:2000SEP08
2000
2062
forward 2
TM
N out


199
LI:288905.4:2000SEP08
99
158
forward 3
TM
N in


200
LI:332161.1:2000SEP08
1507
1587
forward 1
TM
N in


200
LI:332161.1:2000SEP08
1663
1743
forward 1
TM
N in


200
LI:332161.1:2000SEP08
2314
2400
forward 1
TM
N in


200
LI:332161.1:2000SEP08
2890
2940
forward 1
TM
N in


200
LI:332161.1:2000SEP08
776
835
forward 2
TM


200
LI:332161.1:2000SEP08
1340
1393
forward 2
TM


200
LI:332161.1:2000SEP08
1493
1579
forward 2
TM


200
LI:332161.1:2000SEP08
1637
1717
forward 2
TM


200
LI:332161.1:2000SEP08
1880
1966
forward 2
TM


200
LI:332161.1:2000SEP08
2075
2161
forward 2
TM


200
LI:332161.1:2000SEP08
2744
2818
forward 2
TM


200
LI:332161.1:2000SEP08
258
311
forward 3
TM
N in


200
LI:332161.1:2000SEP08
1524
1610
forward 3
TM
N in


200
LI:332161.1:2000SEP08
2025
2111
forward 3
TM
N in


200
LI:332161.1:2000SEP08
2289
2375
forward 3
TM
N in


201
LI:184867.1:2000SEP08
1985
2041
forward 2
TM
N in


201
LI:184867.1:2000SEP08
771
854
forward 3
TM
N out


202
LI:229932.4:2000SEP08
76
162
forward 1
TM
N out


202
LI:229932.4:2000SEP08
229
300
forward 1
TM
N out


202
LI:229932.4:2000SEP08
1249
1329
forward 1
TM
N out


202
LI:229932.4:2000SEP08
1438
1524
forward 1
TM
N out


202
LI:229932.4:2000SEP08
1678
1764
forward 1
TM
N out


202
LI:229932.4:2000SEP08
68
142
forward 2
TM
N out


202
LI:229932.4:2000SEP08
215
271
forward 2
TM
N out


202
LI:229932.4:2000SEP08
734
820
forward 2
TM
N out


202
LI:229932.4:2000SEP08
1220
1291
forward 2
TM
N out


202
LI:229932.4:2000SEP08
1565
1618
forward 2
TM
N out


202
LI:229932.4:2000SEP08
60
146
forward 3
TM


202
LI:229932.4:2000SEP08
348
425
forward 3
TM


202
LI:229932.4:2000SEP08
762
848
forward 3
TM


202
LI:229932.4:2000SEP08
1239
1325
forward 3
TM


202
LI:229932.4:2000SEP08
1401
1487
forward 3
TM


202
LI:229932.4:2000SEP08
1629
1703
forward 3
TM


203
LI:1189932.1:2000SEP08
277
363
forward 1
TM
N out


203
LI:1189932.1:2000SEP08
1141
1203
forward 1
TM
N out


203
LI:1189932.1:2000SEP08
1216
1278
forward 1
TM
N out


203
LI:1189932.1:2000SEP08
1411
1497
forward 1
TM
N out


203
LI:1189932.1:2000SEP08
1642
1707
forward 1
TM
N out


203
LI:1189932.1:2000SEP08
1795
1881
forward 1
TM
N out


203
LI:1189932.1:2000SEP08
2125
2211
forward 1
TM
N out


203
LI:1189932.1:2000SEP08
89
151
forward 2
TM
N in


203
LI:1189932.1:2000SEP08
218
304
forward 2
TM
N in


203
LI:1189932.1:2000SEP08
320
388
forward 2
TM
N in


203
LI:1189932.1:2000SEP08
386
451
forward 2
TM
N in


203
LI:1189932.1:2000SEP08
572
643
forward 2
TM
N in


203
LI:1189932.1:2000SEP08
1142
1222
forward 2
TM
N in


203
LI:1189932.1:2000SEP08
1412
1498
forward 2
TM
N in


203
LI:1189932.1:2000SEP08
1928
1990
forward 2
TM
N in


203
LI:1189932.1:2000SEP08
2021
2107
forward 2
TM
N in


203
LI:1189932.1:2000SEP08
2141
2227
forward 2
TM
N in


203
LI:1189932.1:2000SEP08
522
608
forward 3
TM
N out


203
LI:1189932.1:2000SEP08
858
944
forward 3
TM
N out


203
LI:1189932.1:2000SEP08
1161
1247
forward 3
TM
N out


203
LI:1189932.1:2000SEP08
1992
2066
forward 3
TM
N out


203
LI:1189932.1:2000SEP08
2139
2210
forward 3
TM
N out


204
LI:1076689.1:2000SEP08
43
114
forward 1
TM
N in


204
LI:1076689.1:2000SEP08
326
373
forward 2
TM
N in


205
LI:415181.2:2000SEP08
1033
1113
forward 1
TM
N in


205
LI:415181.2:2000SEP08
1363
1434
forward 1
TM
N in


205
LI:415181.2:2000SEP08
914
1000
forward 2
TM


206
LI:296358.1:2000SEP08
760
819
forward 1
TM
N out


206
LI:296358.1:2000SEP08
997
1068
forward 1
TM
N out


206
LI:296358.1:2000SEP08
1147
1233
forward 1
TM
N out


206
LI:296358.1:2000SEP08
197
247
forward 2
TM
N out


206
LI:296358.1:2000SEP08
356
442
forward 2
TM
N out


207
LI:205186.3:2000SEP08
644
697
forward 2
TM
N in


207
LI:205186.3:2000SEP08
812
877
forward 2
TM
N in


208
LI:220537.2:2000SEP08
595
681
forward 1
TM
N in


208
LI:220537.2:2000SEP08
1429
1515
forward 1
TM
N in


208
LI:220537.2:2000SEP08
245
331
forward 2
TM
N out


208
LI:220537.2:2000SEP08
362
415
forward 2
TM
N out


208
LI:220537.2:2000SEP08
1058
1129
forward 2
TM
N out


208
LI:220537.2:2000SEP08
1136
1222
forward 2
TM
N out


208
LI:220537.2:2000SEP08
1472
1555
forward 2
TM
N out


208
LI:220537.2:2000SEP08
1820
1897
forward 2
TM
N out


208
LI:220537.2:2000SEP08
216
299
forward 3
TM
N out


208
LI:220537.2:2000SEP08
447
509
forward 3
TM
N out


208
LI:220537.2:2000SEP08
522
584
forward 3
TM
N out


208
LI:220537.2:2000SEP08
624
686
forward 3
TM
N out


208
LI:220537.2:2000SEP08
702
764
forward 3
TM
N out


208
LI:220537.2:2000SEP08
1467
1553
forward 3
TM
N out


208
LI:220537.2:2000SEP08
1806
1892
forward 3
TM
N out


209
LI:248364.2:2000SEP08
439
495
forward 1
TM
N out


210
LI:2048338.1:2000SEP08
268
354
forward 1
TM
N in


210
LI:2048338.1:2000SEP08
385
459
forward 1
TM
N in


210
LI:2048338.1:2000SEP08
541
591
forward 1
TM
N in


210
LI:2048338.1:2000SEP08
281
358
forward 2
TM
N in


211
LI:1185203.8:2000SEP08
73
135
forward 1
TM
N out


211
LI:1185203.8:2000SEP08
148
210
forward 1
TM
N out


211
LI:1185203.8:2000SEP08
226
294
forward 1
TM
N out


212
LI:021770.3:2000SEP08
593
673
forward 2
TM
N out


212
LI:021770.3:2000SEP08
348
434
forward 3
TM
N in


212
LI:021770.3:2000SEP08
462
539
forward 3
TM
N in


212
LI:021770.3:2000SEP08
564
641
forward 3
TM
N in


212
LI:021770.3:2000SEP08
861
944
forward 3
TM
N in


213
LI:1185841.1:2000SEP08
1132
1182
forward 1
TM
N out


213
LI:1185841.1:2000SEP08
2434
2520
forward 1
TM
N out


213
LI:1185841.1:2000SEP08
965
1030
forward 2
TM
N in


213
LI:1185841.1:2000SEP08
2381
2437
forward 2
TM
N in


214
LI:1181710.1:2000SEP08
221
307
forward 2
TM
N out


215
LI:2048959.1:2000SEP08
262
318
forward 1
TM
N out


216
LI:798494.1:2000SEP08
595
657
forward 1
TM
N out


216
LI:798494.1:2000SEP08
670
732
forward 1
TM
N out


216
LI:798494.1:2000SEP08
215
268
forward 2
TM
N out


216
LI:798494.1:2000SEP08
12
62
forward 3
TM
N out


216
LI:798494.1:2000SEP08
60
113
forward 3
TM
N out


217
LI:2049223.1:2000SEP08
436
507
forward 1
TM
N in


217
LI:2049223.1:2000SEP08
416
484
forward 2
TM
N out


218
LI:1177833.1:2000SEP08
712
798
forward 1
TM
N in


219
LI:2049267.1:2000SEP08
215
289
forward 2
TM
N out


219
LI:2049267.1:2000SEP08
240
323
forward 3
TM
N out


220
LI:1165939.1:2000SEP08
554
640
forward 2
TM


221
LI:1170958.1:2000SEP08
326
376
forward 2
TM
N out


222
LI:1089827.1:2000SEP08
1507
1584
forward 1
TM
N in


223
LI:792112.1:2000SEP08
818
892
forward 2
TM
N in


223
LI:792112.1:2000SEP08
9
86
forward 3
TM


223
LI:792112.1:2000SEP08
669
755
forward 3
TM


223
LI:792112.1:2000SEP08
783
860
forward 3
TM


224
LI:282219.2:2000SEP08
661
732
forward 1
TM
N out


224
LI:282219.2:2000SEP08
491
577
forward 2
TM
N in


224
LI:282219.2:2000SEP08
659
745
forward 2
TM
N in


224
LI:282219.2:2000SEP08
408
458
forward 3
TM
N in


225
LI:1088010.2:2000SEP08
289
375
forward 1
TM
N in


225
LI:1088010.2:2000SEP08
716
793
forward 2
TM
N in


225
LI:1088010.2:2000SEP08
1229
1315
forward 2
TM
N in


225
LI:1088010.2:2000SEP08
903
980
forward 3
TM
N out


225
LI:1088010.2:2000SEP08
1002
1088
forward 3
TM
N out


225
LI:1088010.2:2000SEP08
1185
1247
forward 3
TM
N out


225
LI:1088010.2:2000SEP08
1272
1334
forward 3
TM
N out


226
LI:1165276.1:2000SEP08
301
363
forward 1
TM
N in


226
LI:1165276.1:2000SEP08
882
968
forward 3
TM
N out


227
LI:1169524.2:2000SEP08
623
709
forward 2
TM


227
LI:1169524.2:2000SEP08
713
778
forward 2
TM


227
LI:1169524.2:2000SEP08
842
928
forward 2
TM


228
LI:1180255.1:2000SEP08
731
784
forward 2
TM
N in


228
LI:1180255.1:2000SEP08
872
931
forward 2
TM
N in


228
LI:1180255.1:2000SEP08
1199
1285
forward 2
TM
N in


229
LI:1091903.1:2000SEP08
454
540
forward 1
TM
N out


230
LI:1169219.1:2000SEP08
496
582
forward 1
TM
N in


230
LI:1169219.1:2000SEP08
509
595
forward 2
TM
N out


230
LI:1169219.1:2000SEP08
495
581
forward 3
TM


231
LI:2050313.1:2000SEP08
2605
2664
forward 1
TM
N in


231
LI:2050313.1:2000SEP08
3229
3315
forward 1
TM
N in


231
LI:2050313.1:2000SEP08
3412
3498
forward 1
TM
N in


231
LI:2050313.1:2000SEP08
1886
1954
forward 2
TM
N in


231
LI:2050313.1:2000SEP08
2654
2731
forward 2
TM
N in


231
LI:2050313.1:2000SEP08
2924
2986
forward 2
TM
N in


231
LI:2050313.1:2000SEP08
3029
3091
forward 2
TM
N in


231
LI:2050313.1:2000SEP08
3482
3568
forward 2
TM
N in


231
LI:2050313.1:2000SEP08
855
920
forward 3
TM
N out


231
LI:2050313.1:2000SEP08
2445
2531
forward 3
TM
N out


231
LI:2050313.1:2000SEP08
2646
2708
forward 3
TM
N out


231
LI:2050313.1:2000SEP08
2721
2783
forward 3
TM
N out


231
LI:2050313.1:2000SEP08
3114
3170
forward 3
TM
N out


231
LI:2050313.1:2000SEP08
3504
3590
forward 3
TM
N out


232
LI:209351.3:2000SEP08
586
645
forward 1
TM
N in


232
LI:209351.3:2000SEP08
1945
2025
forward 1
TM
N in


232
LI:209351.3:2000SEP08
353
415
forward 2
TM


232
LI:209351.3:2000SEP08
665
718
forward 2
TM


232
LI:209351.3:2000SEP08
1313
1387
forward 2
TM


232
LI:209351.3:2000SEP08
1991
2041
forward 2
TM


232
LI:209351.3:2000SEP08
2153
2230
forward 2
TM


232
LI:209351.3:2000SEP08
2390
2443
forward 2
TM


232
LI:209351.3:2000SEP08
801
869
forward 3
TM
N in


232
LI:209351.3:2000SEP08
1926
2006
forward 3
TM
N in


232
LI:209351.3:2000SEP08
2382
2456
forward 3
TM
N in


233
LI:119900.1:2000SEP08
667
744
forward 1
TM
N in


233
LI:119900.1:2000SEP08
521
607
forward 2
TM
N out


233
LI:119900.1:2000SEP08
719
799
forward 2
TM
N out


233
LI:119900.1:2000SEP08
24
98
forward 3
TM


233
LI:119900.1:2000SEP08
678
764
forward 3
TM


234
LI:2052274.1:2000SEP08
332
418
forward 2
TM
N in


234
LI:2052274.1:2000SEP08
1526
1612
forward 2
TM
N in


234
LI:2052274.1:2000SEP08
939
1025
forward 3
TM
N in


234
LI:2052274.1:2000SEP08
1500
1586
forward 3
TM
N in


235
LI:1075502.1:2000SEP08
200
277
forward 2
TM
N in


235
LI:1075502.1:2000SEP08
483
569
forward 3
TM
N in


236
LI:813697.1:2000SEP08
805
867
forward 1
TM


236
LI:813697.1:2000SEP08
224
283
forward 2
TM


236
LI:813697.1:2000SEP08
1638
1715
forward 3
TM
N out


236
LI:813697.1:2000SEP08
1722
1808
forward 3
TM
N out


237
LI:814261.1:2000SEP08
562
618
forward 1
TM


237
LI:814261.1:2000SEP08
287
343
forward 2
TM
N out


237
LI:814261.1:2000SEP08
512
598
forward 2
TM
N out


237
LI:814261.1:2000SEP08
279
356
forward 3
TM
N out


237
LI:814261.1:2000SEP08
474
557
forward 3
TM
N out


238
LI:775334.1:2000SEP08
898
984
forward 1
TM
N in


238
LI:775334.1:2000SEP08
581
661
forward 2
TM
N out


239
LI:1180325.1:2000SEP08
833
919
forward 2
TM
N in


240
LI:1183147.3:2000SEP08
268
342
forward 1
TM
N in


240
LI:1183147.3:2000SEP08
370
456
forward 1
TM
N in


240
LI:1183147.3:2000SEP08
712
798
forward 1
TM
N in


240
LI:1183147.3:2000SEP08
937
1023
forward 1
TM
N in


240
LI:1183147.3:2000SEP08
374
460
forward 2
TM
N in


240
LI:1183147.3:2000SEP08
800
871
forward 2
TM
N in


240
LI:1183147.3:2000SEP08
968
1045
forward 2
TM
N in


240
LI:1183147.3:2000SEP08
1385
1450
forward 2
TM
N in


240
LI:1183147.3:2000SEP08
156
224
forward 3
TM
N out


240
LI:1183147.3:2000SEP08
285
347
forward 3
TM
N out


240
LI:1183147.3:2000SEP08
414
500
forward 3
TM
N out


240
LI:1183147.3:2000SEP08
687
770
forward 3
TM
N out


240
LI:1183147.3:2000SEP08
846
932
forward 3
TM
N out


240
LI:1183147.3:2000SEP08
1002
1067
forward 3
TM
N out


241
LI:1175373.3:2000SEP08
283
357
forward 1
TM
N out


242
LI:813757.1:2000SEP08
744
827
forward 3
TM
N in


243
LI:1182979.2:2000SEP08
370
456
forward 1
TM
N in


243
LI:1182979.2:2000SEP08
742
828
forward 1
TM
N in


243
LI:1182979.2:2000SEP08
705
767
forward 3
TM
N out


243
LI:1182979.2:2000SEP08
783
845
forward 3
TM
N out


244
LI:1177823.2:2000SEP08
307
393
forward 1
TM
N out


244
LI:1177823.2:2000SEP08
311
370
forward 2
TM
N in


245
LI:1174279.1:2000SEP08
634
720
forward 1
TM
N out


245
LI:1174279.1:2000SEP08
724
789
forward 1
TM
N out


246
LI:1178411.1:2000SEP08
1357
1443
forward 1
TM


246
LI:1178411.1:2000SEP08
1290
1376
forward 3
TM
N in


246
LI:1178411.1:2000SEP08
1419
1472
forward 3
TM
N in


247
LI:1182739.1:2000SEP08
853
939
forward 1
TM
N in


247
LI:1182739.1:2000SEP08
1900
1986
forward 1
TM
N in


247
LI:1182739.1:2000SEP08
2131
2217
forward 1
TM
N in


247
LI:1182739.1:2000SEP08
2341
2403
forward 1
TM
N in


247
LI:1182739.1:2000SEP08
2446
2508
forward 1
TM
N in


247
LI:1182739.1:2000SEP08
803
859
forward 2
TM
N in


247
LI:1182739.1:2000SEP08
1268
1351
forward 2
TM
N in


247
LI:1182739.1:2000SEP08
1445
1513
forward 2
TM
N in


247
LI:1182739.1:2000SEP08
1796
1882
forward 2
TM
N in


247
LI:1182739.1:2000SEP08
2090
2176
forward 2
TM
N in


247
LI:1182739.1:2000SEP08
2267
2323
forward 2
TM
N in


247
LI:1182739.1:2000SEP08
2363
2449
forward 2
TM
N in


247
LI:1182739.1:2000SEP08
1182
1244
forward 3
TM
N out


247
LI:1182739.1:2000SEP08
1254
1316
forward 3
TM
N out


247
LI:1182739.1:2000SEP08
2100
2156
forward 3
TM
N out


247
LI:1182739.1:2000SEP08
2301
2387
forward 3
TM
N out


248
LI:234937.4:2000SEP08
301
387
forward 1
TM
N out


249
LI:1170660.1:2000SEP08
604
690
forward 1
TM
N in


249
LI:1170660.1:2000SEP08
757
843
forward 1
TM
N in


249
LI:1170660.1:2000SEP08
937
990
forward 1
TM
N in


249
LI:1170660.1:2000SEP08
1111
1179
forward 1
TM
N in


249
LI:1170660.1:2000SEP08
512
583
forward 2
TM


249
LI:1170660.1:2000SEP08
911
973
forward 2
TM


249
LI:1170660.1:2000SEP08
986
1048
forward 2
TM


249
LI:1170660.1:2000SEP08
252
323
forward 3
TM
N out


249
LI:1170660.1:2000SEP08
591
677
forward 3
TM
N out


249
LI:1170660.1:2000SEP08
774
860
forward 3
TM
N out


250
LI:1144409.1:2000SEP08
25
81
forward 1
TM
N out


250
LI:1144409.1:2000SEP08
1708
1782
forward 1
TM
N out


250
LI:1144409.1:2000SEP08
2281
2367
forward 1
TM
N out


250
LI:1144409.1:2000SEP08
1658
1744
forward 2
TM
N in


250
LI:1144409.1:2000SEP08
1880
1927
forward 2
TM
N in


250
LI:1144409.1:2000SEP08
2294
2380
forward 2
TM
N in


250
LI:1144409.1:2000SEP08
1614
1697
forward 3
TM
N in


250
LI:1144409.1:2000SEP08
2217
2303
forward 3
TM
N in


251
LI:246290.10:2000SEP08
248
304
forward 2
TM
N out


251
LI:246290.10:2000SEP08
641
727
forward 2
TM
N out


251
LI:246290.10:2000SEP08
3
89
forward 3
TM
N out


252
LI:280034.1:2000SEP08
279
365
forward 3
TM
N out










[0304]

6









TABLE 5








SEQ ID NO:
Template ID
Component ID
Start
Stop



















1
LG:150318.1:2000SEP08
482540R6
1
350


1
LG:150318.1:2000SEP08
482540H1
1
238


1
LG:150318.1:2000SEP08
6021134T8
126
531


1
LG:150318.1:2000SEP08
6021134R8
126
537


1
LG:150318.1:2000SEP08
6021134H1
126
629


2
LG:022529.1:2000SEP08
7593029H1
1
521


2
LG:022529.1:2000SEP08
g1645695
112
517


2
LG:022529.1:2000SEP08
2160267H1
275
514


2
LG:022529.1:2000SEP08
5284828H1
309
583


2
LG:022529.1:2000SEP08
g1880347
313
601


2
LG:022529.1:2000SEP08
7352207H1
330
707


2
LG:022529.1:2000SEP08
6863346H1
339
830


2
LG:022529.1:2000SEP08
3351341H1
423
681


2
LG:022529.1:2000SEP08
077299H1
432
632


2
LG:022529.1:2000SEP08
078146H1
438
646


2
LG:022529.1:2000SEP08
3801790F6
523
1030


2
LG:022529.1:2000SEP08
3801790H1
523
823


2
LG:022529.1:2000SEP08
3769238F6
523
1043


2
LG:022529.1:2000SEP08
3802590H1
524
810


2
LG:022529.1:2000SEP08
6217218H1
549
1039


2
LG:022529.1:2000SEP08
g5743872
664
1137


2
LG:022529.1:2000SEP08
g3051534
685
1047


2
LG:022529.1:2000SEP08
g4195758
789
1045


3
LG:352559.1:2000SEP08
6453567H1
1
503


3
LG:352559.1:2000SEP08
4052122H1
185
457


3
LG:352559.1:2000SEP08
4052122F7
185
636


3
LG:352559.1:2000SEP08
g3897399
255
371


4
LG:175223.1:2000SEP08
3081155F6
1
417


4
LG:175223.1:2000SEP08
3081155H1
2
315


4
LG:175223.1:2000SEP08
3081155T6
31
465


4
LG:175223.1:2000SEP08
g1648354
58
457


4
LG:175223.1:2000SEP08
5800009H1
99
507


5
LG:476989.1:2000SEP08
6874941H1
1
169


5
LG:476989.1:2000SEP08
6874955H1
1
204


5
LG:476989.1:2000SEP08
g4393499
51
432


5
LG:476989.1:2000SEP08
g4190810
96
432


6
LG:253268.7:2000SEP08
6772515H1
607
1083


6
LG:253268.7:2000SEP08
g5526194
596
941


6
LG:253268.7:2000SEP08
g4729197
690
941


6
LG:253268.7:2000SEP08
g5809986
501
941


6
LG:253268.7:2000SEP08
g2540947
535
937


6
LG:253268.7:2000SEP08
g922062
586
935


6
LG:253268.7:2000SEP08
6772515J1
454
961


6
LG:253268.7:2000SEP08
2535554F6
493
929


6
LG:253268.7:2000SEP08
g4392225
520
923


6
LG:253268.7:2000SEP08
g3424830
561
923


6
LG:253268.7:2000SEP08
g4533991
464
923


6
LG:253268.7:2000SEP08
g885146
693
914


6
LG:253268.7:2000SEP08
g917418
564
914


6
LG:253268.7:2000SEP08
g888754
605
914


6
LG:253268.7:2000SEP08
g922196
606
913


6
LG:253268.7:2000SEP08
g888391
595
912


6
LG:253268.7:2000SEP08
g5364213
457
897


6
LG:253268.7:2000SEP08
g990349
560
886


6
LG:253268.7:2000SEP08
g888707
589
884


6
LG:253268.7:2000SEP08
g885121
574
884


6
LG:253268.7:2000SEP08
g888978
669
883


6
LG:253268.7:2000SEP08
g990350
535
881


6
LG:253268.7:2000SEP08
6852955H1
306
854


6
LG:253268.7:2000SEP08
7236518H1
249
789


6
LG:253268.7:2000SEP08
2535554H1
493
737


6
LG:253268.7:2000SEP08
g889930
353
601


6
LG:253268.7:2000SEP08
g888417
353
587


6
LG:253268.7:2000SEP08
5773584H1
69
569


6
LG:253268.7:2000SEP08
488757R1
1
536


7
LG:401322.1:2000SEP08
4875149T6
344
737


7
LG:401322.1:2000SEP08
g3202357
457
784


7
LG:401322.1:2000SEP08
748032H1
574
776


7
LG:401322.1:2000SEP08
750543H1
1
183


7
LG:401322.1:2000SEP08
g1474315
42
323


7
LG:401322.1:2000SEP08
3722596H1
61
333


7
LG:401322.1:2000SEP08
4875149F6
70
195


7
LG:401322.1:2000SEP08
4875149H1
70
257


7
LG:401322.1:2000SEP08
6561179H1
71
633


7
LG:401322.1:2000SEP08
2029094R6
110
485


7
LG:401322.1:2000SEP08
2029094H1
121
372


7
LG:401322.1:2000SEP08
5950410H1
125
401


7
LG:401322.1:2000SEP08
5950630H1
125
405


7
LG:401322.1:2000SEP08
g4998660
180
478


7
LG:401322.1:2000SEP08
4933727H1
239
384


7
LG:401322.1:2000SEP08
3533254H1
273
564


8
LG:1328436.1:2000SEP08
2505871H1
1
210


8
LG:1328436.1:2000SEP08
6200837H1
4
346


8
LG:1328436.1:2000SEP08
6201568T8
26
343


8
LG:1328436.1:2000SEP08
6201568H1
26
629


8
LG:1328436.1:2000SEP08
6201568F8
26
211


8
LG:1328436.1:2000SEP08
g2630885
36
432


8
LG:1328436.1:2000SEP08
g723429
7
191


8
LG:1328436.1:2000SEP08
6200837T8
76
343


8
LG:1328436.1:2000SEP08
g725043
91
362


8
LG:1328436.1:2000SEP08
g725147
312
572


9
LG:475404.1:2000SEP08
460544H1
20
245


9
LG:475404.1:2000SEP08
5998240H1
1
484


9
LG:475404.1:2000SEP08
5998240T8
1
408


9
LG:475404.1:2000SEP08
5998240F8
1
398


9
LG:475404.1:2000SEP08
455966H1
20
255


9
LG:475404.1:2000SEP08
455162H1
20
272


9
LG:475404.1:2000SEP08
455162R6
20
521


9
LG:475404.1:2000SEP08
458061H1
20
259


9
LG:475404.1:2000SEP08
460544R6
20
326


9
LG:475404.1:2000SEP08
3206542H1
25
202


9
LG:475404.1:2000SEP08
4663964H1
37
289


9
LG:475404.1:2000SEP08
7652675J1
47
172


9
LG:475404.1:2000SEP08
g1807165
81
278


9
LG:475404.1:2000SEP08
g2401959
129
486


9
LG:475404.1:2000SEP08
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LG:475404.1:2000SEP08
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LG:1384132.1:2000SEP08
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LG:1384132.1:2000SEP08
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LG:1384132.1:2000SEP08
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LG:410804.18:2000SEP08
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LG:1082306.1:2000SEP08
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LG:1082306.1:2000SEP08
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LG:1082306.1:2000SEP08
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LG:1082306.1:2000SEP08
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LG:1082306.1:2000SEP08
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LG:1082306.1:2000SEP08
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LG:1082306.1:2000SEP08
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LG:1082306.1:2000SEP08
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12
LG:1082306.1:2000SEP08
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LG:1082306.1:2000SEP08
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LG:1082306.1:2000SEP08
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723


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LG:1082306.1:2000SEP08
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LG:233814.4:2000SEP08
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LG:233814.4:2000SEP08
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LG:233814.4:2000SEP08
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927


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LG:233814.4:2000SEP08
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LG:233814.4:2000SEP08
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LG:233814.4:2000SEP08
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LG:977478.5:2000SEP08
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LG:977478.5:2000SEP08
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LG:977478.5:2000SEP08
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14
LG:977478.5:2000SEP08
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LG:977478.5:2000SEP08
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14
LG:977478.5:20003EP08
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LG:977478.5:2000SEP08
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LG:977478.5:2000SEP08
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LG:977478.5:2000SEP08
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LG:977478.5:2000SEP08
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LG:977478.5:2000SEP08
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LG:977478.5:2000SEP08
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LG:025931.1:2000SEP08
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LG:025931.1:2000SEP08
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LG:025931.1:2000SEP08
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LG:025931.1:2000SEP08
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LG:025931.1:2000SEP08
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LG:025931.1:2000SEP08
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LG:025931.1:2000SEP08
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LG:025931.1:2000SEP08
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LG:025931.1:2000SEP08
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LG:025931.1:2000SEP08
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LG:885368.1:2000SEP08
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LG:885368.1:2000SEP08
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LG:885368.1:2000SEP08
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LG:885368.1:2000SEP08
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LG:885368.1:2000SEP08
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LG:885368.1:2000SEP08
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LG:885368.1:2000SEP08
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LG:885368.1:2000SEP08
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LG:885368.1:2000SEP08
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LG:1054900.1:2000SEP08
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LG:1054900.1:2000SEP08
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17
LG:1054900.1:2000SEP08
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LG:1054900.1:2000SEP08
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17
LG:1054900.1:2000SEP08
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LG:1054900.1:2000SEP08
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LG:1054900.1:2000SEP08
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LG:995186.2:2000SEP08
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LG:995186.2:2000SEP08
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LG:435048.23:2000SEP08
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LG:435048.23:2000SEP08
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LG:954859.1:2000SEP08
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20
LG:954859.1:2000SEP08
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LG:954859.1:2000SEP08
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LG:954859.1:2000SEP08
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LG:954859.1:2000SEP08
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20
LG:954859.1:2000SEP08
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LG:364370.1:2000SEP08
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LG:364370.1:2000SEP08
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LG:364370.1:2000SEP08
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LG:364370.1:2000SEP08
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21
LG:364370.1:2000SEP08
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21
LG:364370.1:2000SEP08
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21
LG:364370.1:2000SEP08
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22
LG:1098789.1:2000SEP08
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LG:201540.2:2000SEP08
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23
LG:201540.2:2000SEP08
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LG:201540.2:2000SEP08
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23
LG:201540.2:2000SEP08
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23
LG:201540.2:2000SEP08
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23
LG:201540.2:2000SEP08
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23
LG:201540.2:2000SEP08
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23
LG:201540.2:2000SEP08
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23
LG:201540.2:2000SEP08
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23
LG:201540.2:2000SEP08
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23
LG:201540.2:2000SEP08
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23
LG:201540.2:2000SEP08
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733
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23
LG:201540.2:2000SEP08
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23
LG:201540.2:2000SEP08
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23
LG:201540.2:2000SEP08
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23
LG:201540.2:2000SEP08
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23
LG:201540.2:2000SEP08
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23
LG:201540.2:2000SEP08
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23
LG:201540.2:2000SEP08
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308
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23
LG:201540.2:2000SEP08
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23
LG:201540.2:2000SEP08
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23
LG:201540.2:2000SEP08
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1093


23
LG:201540.2:2000SEP08
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23
LG:201540.2:2000SEP08
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23
LG:201540.2:2000SEP08
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LG:201540.2:2000SEP08
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24
LG:1077357.1:2000SEP08
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LG:1077357.1:2000SEP08
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LG:1077357.1:2000SEP08
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LG:1077357.1:2000SEP08
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24
LG:1077357.1:2000SEP08
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24
LG:1077357.1:2000SEP08
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LG:1048846.4:2000SEP08
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LG:1048846.4:2000SEP08
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25
LG:1048846.4:2000SEP08
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191
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25
LG:1048846.4:2000SEP08
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213
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25
LG:1048846.4:2000SEP08
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LG:1048846.4:2000SEP08
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LG:336685.1:2000SEP08
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LG:336685.1:2000SEP08
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LG:336685.1:2000SEP08
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LG:336685.1:2000SEP08
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LG:336685.1:2000SEP08
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LG:336685.1:2000SEP08
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LG:336685.1:2000SEP08
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LG:336685.1:2000SEP08
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LG:336685.1:2000SEP08
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LG:336685.1:2000SEP08
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26
LG:336685.1:2000SEP08
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LG:1076253.1:2000SEP08
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27
LG:1076253.1:2000SEP08
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LG:1076253.1:2000SEP08
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LG:1076253.1:2000SEP08
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LG:1076253.1:2000SEP08
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LG:1076253.1:2000SEP08
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27
LG:1076253.1:2000SEP08
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389
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27
LG:1076253.1:2000SEP08
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27
LG:1076253.1:2000SEP08
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27
LG:1076253.1:2000SEP08
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27
LG:1076253.1:2000SEP08
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27
LG:1076253.1:2000SEP08
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27
LG:1076253.1:2000SEP08
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27
LG:1076253.1:2000SEP08
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27
LG:1076253.1:2000SEP08
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LG:1400601.2:2000SEP08
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LG:1079092.3:2000SEP08
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29
LG:1079092.3:2000SEP08
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30
LG:1086064.1:2000SEP08
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30
LG:1086064.1:2000SEP08
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30
LG:1086064.1:2000SEP08
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30
LG:1086064.1:2000SEP08
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30
LG:1086064.1:2000SEP08
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30
LG:1086064.1:2000SEP08
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30
LG:1086064.1:2000SEP08
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30
LG:1086064.1:2000SEP08
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30
LG:1086064.1:2000SEP08
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30
LG:1086064.1:2000SEP08
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30
LG:1086064.1:2000SEP08
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127
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30
LG:1086064.1:2000SEP08
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30
LG:1086064.1:2000SEP08
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30
LG:1086064.1:2000SEP08
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LG:1086064.1:2000SEP08
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30
LG:1086064.1:2000SEP08
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30
LG:1086064.1:2000SEP08
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LG:1086064.1:2000SEP08
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LG:1086064.1:2000SEP08
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LG:1086064.1:2000SEP08
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LG:1086064.1:2000SEP08
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LG:1086064.1:2000SEP08
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LG:1086064.1:2000SEP08
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LG:1086064.1:2000SEP08
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LG:1086064.1:2000SEP08
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30
LG:1086064.1:2000SEP08
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LG:1086064.1:2000SEP08
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30
LG:1086064.1:2000SEP08
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30
LG:1086064.1:2000SEP08
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30
LG:1086064.1:2000SEP08
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30
LG:1086064.1:2000SEP08
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LG:1400608.1:2000SEP08
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31
LG:1400608.1:2000SEP08
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31
LG:1400608.1:2000SEP08
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31
LG:1400608.1:2000SEP08
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31
LG:1400608.1:2000SEP08
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31
LG:1400608.1:2000SEP08
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31
LG:1400608.1:2000SEP08
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31
LG:1400608.1:2000SEP08
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31
LG:1400608.1:2000SEP08
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31
LG:1400608.1:2000SEP08
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31
LG:1400608.1:2000SEP08
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LG:399275.5:2000SEP08
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32
LG:399275.5:2000SEP08
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32
LG:399275.5:2000SEP08
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32
LG:399275.5:2000SEP08
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LG:293943.1:2000SEP08
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33
LG:293943.1:2000SEP08
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LG:293943.1:2000SEP08
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33
LG:293943.1:2000SEP08
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33
LG:293943.1:2000SEP08
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33
LG:293943.1:2000SEP08
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34
LG:345884.1:2000SEP08
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34
LG:345884.1:2000SEP08
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LG:345884.1:2000SEP08
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34
LG:345884.1:2000SEP08
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LG:345884.1:2000SEP08
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LG:345884.1:2000SEP08
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LG:400967.1:2000SEP08
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LG:400967.1:2000SEP08
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LG:400967.1:2000SEP08
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LG:400967.1:2000SEP08
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35
LG:400967.1:2000SEP08
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35
LG:400967.1:2000SEP08
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35
LG:400967.1:2000SEP08
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35
LG:400967.1:2000SEP08
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LG:400967.1:2000SEP08
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LG:024556.6:2000SEP08
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LG:024556.6:2000SEP08
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LG:024556.6:2000SEP08
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36
LG:024556.6:2000SEP08
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LG:024556.6:2000SEP08
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LG:024556.6:2000SEP08
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LG:024556.6:2000SEP08
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LG:024556.6:2000SEP08
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LG:024556.6:2000SEP08
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36
LG:024556.6:2000SEP08
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LG:024556.6:2000SEP08
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LG:024556.6:2000SEP08
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LG:024556.6:2000SEP08
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LG:024556.6:2000SEP08
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36
LG:024556.6:2000SEP08
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36
LG:024556.6:2000SEP08
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LG:024556.6:2000SEP08
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36
LG:024556.6:2000SEP08
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LG:081189.3:2000SEP08
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LG:081189.3:2000SEP08
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LG:081189.3:2000SEP08
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LG:081189.3:2000SEP08
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LG:081189.3:2000SEP08
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LG:081189.3:2000SEP08
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LG:081189.3:2000SEP08
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LG:081189.3:2000SEP08
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LG:081189.3:2000SEP08
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LG:018258.1:2000SEP08
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LG:018258.1:2000SEP08
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LG:018258.1:2000SEP08
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LG:018258.1:2000SEP08
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LG:018258.1:2000SEP08
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LG:018258.1:2000SEP08
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LG:018258.1:2000SEP08
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LG:450399.3:2000SEP08
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LG:450399.3:2000SEP08
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LG:450399.3:2000SEP08
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LG:450399.3:2000SEP08
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39
LG:450399.3:2000SEP08
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39
LG:450399.3:2000SEP08
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40
LG:451122.1:2000SEP08
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5
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40
LG:451122.1:2000SEP08
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40
LG:451122.1:2000SEP08
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40
LG:451122.1:2000SEP08
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40
LG:451122.1:2000SEP08
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40
LG:451122.1:2000SEP08
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40
LG:451122.1:2000SEP08
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5
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40
LG:451122.1:2000SEP08
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LG:451682.1:2000SEP08
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LG:451682.1:2000SEP08
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41
LG:451682.1:2000SEP08
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41
LG:451682.1:2000SEP08
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42
LG:238631.4:2000SEP08
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42
LG:238631.4:2000SEP08
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42
LG:238631.4:2000SEP08
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42
LG:238631.4:2000SEP08
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42
LG:238631.4:2000SEP08
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42
LG:238631.4:2000SEP08
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42
LG:238631.4:2000SEP08
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12
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42
LG:238631.4:2000SEP08
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86
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42
LG:238631.4:2000SEP08
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292
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42
LG:238631.4:2000SEP08
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384
846


42
LG:238631.4:2000SEP08
g4070653
392
850


42
LG:238631.4:2000SEP08
g3665831
396
847


42
LG:238631.4:2000SEP08
g3246602
400
858


42
LG:238631.4:2000SEP08
g2161232
410
665


42
LG:238631.4:2000SEP08
g4525307
437
848


42
LG:238631.4:2000SEP08
g1404313
467
847


42
LG:238631.4:2000SEP08
g3253470
464
858


42
LG:238631.4:2000SEP08
g3250117
469
847


42
LG:238631.4:2000SEP08
g2269451
484
847


42
LG:238631.4:2000SEP08
g3735117
484
845


42
LG:238631.4:2000SEP08
g4223250
506
848


42
LG:238631.4:2000SEP08
g5766307
542
847


42
LG:238631.4:2000SEP08
g3737372
551
847


42
LG:238631.4:2000SEP08
g3016184
580
858


42
LG:238631.4:2000SEP08
g3734551
604
845


42
LG:238631.4:2000SEP08
g5447167
621
845


42
LG:238631.4:2000SEP08
g4762162
621
845


42
LG:238631.4:2000SEP08
g1231962
670
848


42
LG:238631.4:2000SEP08
2406581H1
12
116


42
LG:238631.4:2000SEP08
3401789H1
13
239


42
LG:238631.4:2000SEP08
4648809H1
13
297


42
LG:238631.4:2000SEP08
3634010H1
15
201


42
LG:238631.4:2000SEP08
4653815H1
16
316


42
LG:238631.4:2000SEP08
3152423H1
13
281


42
LG:238631.4:2000SEP08
4414637H1
12
275


42
LG:238631.4:2000SEP08
6121345H1
14
648


42
LG:238631.4:2000SEP08
3428203H1
15
274


42
LG:238631.4:2000SEP08
3744645H1
16
309


42
LG:238631.4:2000SEP08
2698861H1
18
305


42
LG:238631.4:2000SEP08
4143702H1
18
299


42
LG:238631.4:2000SEP08
3995879H1
18
309


42
LG:238631.4:2000SEP08
1830216H1
18
247


42
LG:238631.4:2000SEP08
2998645H1
19
295


42
LG:238631.4:2000SEP08
5464919H1
19
306


42
LG:238631.4:2000SEP08
1713036H1
19
257


42
LG:238631.4:2000SEP08
6116806H1
19
314


42
LG:238631.4:2000SEP08
5788396H1 19
305


42
LG:238631.4:2000SEP08
5121572H1
19
299


42
LG:238631.4:2000SEP08
4715287H1
20
256


42
LG:238631.4:2000SEP08
6197104H1
23
561


42
LG:238631.4:2000SEP08
493734H1
28
246


42
LG:238631.4:2000SEP08
3988991H1
40
341


42
LG:238631.4:2000SEP08
2048688H1
59
314


42
LG:238631.4:2000SEP08
2757550H1
59
328


42
LG:238631.4:2000SEP08
2755553H1
59
330


43
LG:236654.1:2000SEP08
670448T6
802
1151


43
LG:236654.1:2000SEP08
677184R6
802
1154


43
LG:236654.1:2000SEP08
g2810503
842
1188


43
LG:236654.1:2000SEP08
g2336018
909
1189


43
LG:236654.1:2000SEP08
2892611H1
947
1180


43
LG:236654.1:2000SEP08
1289991H1
1083
1189


43
LG:236654.1:2000SEP08
g1979821
1
187


43
LG:236654.1:2000SEP08
g3835204
1
325


43
LG:236654.1:2000SEP08
g6990824
1
298


43
LG:236654.1:2000SEP08
g6704413
1
299


43
LG:236654.1:2000SEP08
6757618J1
8
93


43
LG:236654.1:2000SEP08
7604986J1
9
544


43
LG:236654.1:2000SEP08
g4072180
18
469


43
LG:236654.1:2000SEP08
3519808H1
80
368


43
LG:236654.1:2000SEP08
g843784
234
500


43
LG:236654.1:2000SEP08
1614746F6
288
734


43
LG:236654.1:2000SEP08
1614746H1
288
506


43
LG:236654.1:2000SEP08
7604986H1
364
845


43
LG:236654.1:2000SEP08
1575232H1
366
578


43
LG:236654.1:2000SEP08
g2209653
404
914


43
LG:236654.1:2000SEP08
6322462H1
521
720


43
LG:236654.1:2000SEP08
2892611T6
647
1138


43
LG:236654.1:2000SEP08
g5660108
723
1188


43
LG:236654.1:2000SEP08
1614746T6
735
1150


43
LG:236654.1:2000SEP08
g5365441
749
1190


43
LG:236654.1:2000SEP08
g3644249
768
1191


43
LG:236654.1:2000SEP08
677184H1
802
1073


43
LG:236654.1:2000SEP08
670448R6
802
1188


43
LG:236654.1:2000SEP08
670448H1
802
1057


44
LG:332655.1:2000SEP08
570522H1
606
876


44
LG:332655.1:2000SEP08
3872248T6
663
1142


44
LG:332655.1:2000SEP08
2850393T6
700
1142


44
LG:332655.1:2000SEP08
g2835010
716
1069


44
LG:332655.1:2000SEP08
g4763947
847
1144


44
LG:332655.1:2000SEP08
g4986367
978
1144


44
LG:332655.1:2000SEP08
g5661482
980
1142


44
LG:332655.1:2000SEP08
516193H1
1027
1136


44
LG:332655.1:2000SEP08
5070935H1
498
757


44
LG:332655.1:2000SEP08
g1959326
479
914


44
LG:332655.1:2000SEP08
g1947735
206
551


44
LG:332655.1:2000SEP08
3096881H1
265
401


44
LG:332655.1:2000SEP08
3098886H1
275
541


44
LG:332655.1:2000SEP08 7600091H1
314
782


44
LG:332655.1:2000SEP08
2850393F6
1 499


44
LG:332655.1:2000SEP08
2850393H1
2
289


44
LG:332655.1:2000SEP08
861289H1
3
241


44
LG:332655.1:2000SEP08
2287640R6
5
485


44
LG:332655.1:2000SEP08
2287640H1
5
255


44
LG:332655.1:2000SEP08
3872248F6
11
517


44
LG:332655.1:2000SEP08
3872248H1
11
301


44
LG:332655.1:2000SEP08
3403385H1
114
366


44
LG:332655.1:2000SEP08
1821848H1
133
370


44
LG:332655.1:2000SEP08
3531915H1
153
445


44
LG:332655.1:2000SEP08
2059050H1
160
405


44
LG:332655.1:2000SEP08
5742858H1
164
474


44
LG:332655.1:2000SEP08
2733553H1
185
415


44
LG:332655.1:2000SEP08
5025820H1
188
470


45
LG:217396.2:2000SEP08
5628336R6
940
1483


45
LG:217396.2:2000SEP08
6265192H1
695
1273


45
LG:217396.2:2000SEP08
5868595H1
984
1252


45
LG:217396.2:2000SEP08
5868595F6
972
1252


45
LG:217396.2:2000SEP08
g1187240
976
1186


45
LG:217396.2:2000SEP08
7676247J2
625
1182


45
LG:217396.2:2000SEP08
7706403H1
548
1138


45
LG:217396.2:2000SEP08
g1195854
640
960


45
LG:217396.2:2000SEP08
7351185H1
427
957


45
LG:217396.2:2000SEP08
g4648085
606
876


45
LG:217396.2:2000SEP08
5071261H1
578
837


45
LG:217396.2:2000SEP08
5071261F6
578
824


45
LG:217396.2:2000SEP08
g1921151
518
739


45
LG:217396.2:2000SEP08
6875193H1
159
671


45
LG:21 7396.2:2000SEP08
6989406H1
250
649


45
LG:217396.2:2000SEP08
g1921152
105
513


45
LG:217396.2:2000SEP08
2996140F6
1
621


45
LG:217396.2:2000SEP08
g2818339
123
530


45
LG:217396.2:2000SEP08
3750696H1
232
517


45
LG:217396.2:2000SEP08
7676247H2
1
401


45
LG:217396.2:2000SEP08
5071261T6
1
375


45
LG:217396.2:2000SEP08
2996140H1
1
265


46
LG:090574.1:2000SEP08
2659966F6
1
192


46
LG:090574.1:2000SEP08
2659966T6
1
194


46
LG:090574.1:2000SEP08
2659966H1
1
247


47
LG:202943.1:2000SEP08
1226590R6
174
583


47
LG:202943.1:2000SEP08
5639884H1
136
365


47
LG:202943.1:2000SEP08
1226590T6
383
888


47
LG:202943.1:2000SEP08
5092132H1
515
763


47
LG:202943.1:2000SEP08
1226590H1
174
418


47
LG:202943.1:2000SEP08
g2020858
180
420


47
LG:202943.1:2000SEP08
7213845H1
242
792


47
LG:202943.1:2000SEP08
2579002H2
975
1177


47
LG:202943.1:2000SEP08
6472564H1
942
1357


47
LG:202943.1:2000SEP08
7151349H1
58
561


47
LG:202943.1:2000SEP08
5089408H1
1
270


47
LG:202943.1:2000SEP08
5091008H1
1
269


47
LG:202943.1:2000SEP08
7594783H1
818
1226


47
LG:202943.1:2000SEP08
6469878H1
624
1185


47
LG:202943.1:2000SEP08
5092608H1
1
274


48
LG:236928.1:2000SEP08
3227840H1
1509
1789


48
LG:236928.1:2000SEP08
2487371H1
1524
1754


48
LG:236928.1:2000SEP08
2908866H1
1579
1768


48
LG:236928.1:2000SEP08
g2538920
1584
1877


48
LG:236928.1:2000SEP08
487800H1
1633
1905


48
LG:236928.1:2000SEP08
5404331H1
1669
1966


48
LG:236928.1:2000SEP08
2904955T6
1672
2110


48
LG:236928.1:2000SEP08
4243773H1
1679
1938


48
LG:236928.1:2000SEP08
2904624H1
1682
1978


48
LG:236928.1:2000SEP08
g4990382
1689
2149


48
LG:236928.1:2000SEP08
3291485T6
1692
2110


48
LG:236928.1:2000SEP08
7365257H1
1694
2145


48
LG:236928.1:2000SEP08
g3144565
1717
2158


48
LG:236928.1:2000SEP08
g3144841
1723
2149


48
LG:236928.1:2000SEP08
7761153H1
1
630


48
LG:236928.1:2000SEP08
2905587H1
26
296


48
LG:236928.1:2000SEP08
7741081H1
173
752


48
LG:236928.1:2000SEP08
1491957H1
180
280


48
LG:236928.1:2000SEP08
4741520H1
195
447


48
LG:236928.1:2000SEP08
4741520F6
195
579


48
LG:236928.1:2000SEP08
6616428H1
203
717


48
LG:236928.1:2000SEP08
4697183H1
235
483


48
LG:236928.1:2000SEP08
4697183F6
235
679


48
LG:236928.1:2000SEP08
4028773H1
432
694


48
LG:236928.1:2000SEP08
4028773F8
441
957


48
LG:236928.1:2000SEP08
7761153J1
472
1051


48
LG:236928.1:2000SEP08
7109534H1 524
1104


48
LG:236928.1:2000SEP08
3291 485F6
798
1256


48
LG:236928.1:2000SEP08
2285984H1
798
1018


48
LG:236928.1:2000SEP08
3291485H1
800
1044


48
LG:236928.1:2000SEP08
6842952H1
822
1148


48
LG:236928.1:2000SEP08
6018945H1
841
1148


48
LG:236928.1:2000SEP08
6616428J1
847
1412


48
LG:236928.1:2000SEP08
4785174H1
867
1127


48
LG:236928.1:2000SEP08
2904955F6
1086
1487


48
LG:236928.1:2000SEP08
2904955H1
1086
1380


48
LG:236928.1:2000SEP08
g3163646
1101
1348


48
LG:236928.1:2000SEP08
2918045H1
1170
1452


48
LG:236928.1:2000SEP08
4740283H1
1210
1470


48
LG:236928.1:2000SEP08
g1962038
1291
1631


48
LG:236928.1:2000SEP08
1251534H1
1448
1674


48
LG:236928.1:2000SEP08
1251534F6
1448
1853


48
LG:236928.1:2000SEP08
2556286H1
1483
1733


48
LG:236928.1:2000SEP08
6131688H1
1790
2071


48
LG:236928.1:2000SEP08
g3679201
1791
2159


48
LG:236928.1:2000SEP08
2919136H1
1807
2066


48
LG:236928.1:2000SEP08
6442673H1
1814
2356


48
LG:236928.1:2000SEP08
6870682H1
1869
2347


48
LG:236928.1:2000SEP08
6438933H1
1871
2347


48
LG:236928.1:2000SEP08
645255H1
1877
2114


48
LG:236928.1:2000SEP08
1251534T7
1922
2108


48
LG:236928.1:2000SEP08
2288452H1
1966
2122


48
LG:236928.1:2000SEP08
6855869H1
1968
2537


48
LG:236928.1:2000SEP08
1296086F6
2002
2338


48
LG:236928.1:2000SEP08
1296086H1
2002
2237


48
LG:236928.1:2000SEP08
5021561H1
2022
2302


48
LG:236928.1:2000SEP08
6616156H1
2040
2488


48
LG:236928.1:2000SEP08
g1624634
2135
2305


48
LG:236928.1:2000SEP08
3638554H1
2167
2353


48
LG:236928.1:2000SEP08
3356574H1
2207
2428


48
LG:236928.1:2000SEP08
531771R6
2245
2582


48
LG:236928.1:2000SEP08
531771H1
2245
2486


48
LG:236928.1:2000SEP08
2556128F6
2315
2567


48
LG:236928.1:2000SEP08
2556128H1
2315
2566


48
LG:236928.1:2000SEP08
g1186813
2339
2535


48
LG:236928.1:2000SEP08
2781958H1
2345
2603


48
LG:236928.1:2000SEP08
4748766H1
2371
2635


48
LG:236928.1:2000SEP08
4748737H1
2371
2635


48
LG:236928.1:2000SEP08
3563133H1
2372
2566


48
LG:236928.1:2000SEP08
531771T6
2411
2935


48
LG:236928.1:2000SEP08
5021561T1
2492
2929


48
LG:236928.1:2000SEP08
1269755F6
2505
2772


48
LG:236928.1:2000SEP08
1269755H1
2505
2761


48
LG:236928.1:2000SEP08
1269755F1
2505
2873


48
LG:236928.1:2000SEP08
1269755T6
2506
2934


48
LG:236928.1:2000SEP08
556128T6
2511
2933


48
LG:236928.1:2000SEP08
g2106737
2522
2954


48
LG:236928.1:2000SEP08
6138111H1
2539
2849


48
LG:236928.1:2000SEP08
g3179767
2580
2982


48
LG:236928.1:2000SEP08
727813H1
2595
2826


48
LG:236928.1:2000SEP08
4367390H2
2598
2853


48
LG:236928.1:2000SEP08
g1190057
2621
2982


48
LG:236928.1:2000SEP08
g4986351
2683
2973


48
LG:236928.1:2000SEP08
92526245
2756
2973


48
LG:236928.1:2000SEP08
1717327T6
2855
3383


48
LG:236928.1:2000SEP08
1717327H1
2862
3109


48
LG:236928.1:2000SEP08
1717327F6
2862
3351


49
LG:215169.2:2000SEP08
6037163H1
602
1129


49
LG:215169.2:2000SEP08
6207071H1
928
1536


49
LG:215169.2:2000SEP08
7098455H1
1246
1637


49
LG:215169.2:2000SEP08
6970186H1
1305
1880


49
LG:215169.2:2000SEP08
g5176731
1
212


49
LG:215169.2:2000SEP08
g5431398
1
377


49
LG:215169.2:2000SEP08
g4114328
1
456


49
LG:215169.2:2000SEP08
g6704290
1
472


49
LG:215169.2:2000SEP08
6477953H1
1373
1881


49
LG:215169.2:2000SEP08
7714805H1
1384
1978


49
LG:215169.2:2000SEP08
1486266H1
1519
1767


49
LG:215169.2:2000SEP08
2843912H1
1718
1991


49
LG:215169.2:2000SEP08
1384143H1
1883
2133


49
LG:215169.2:2000SEP08
4901661H1
436
630


49
LG:215169.2:2000SEP08
4901661F6
436
633


49
LG:215169.2:2000SEP08
7269396H1
112
652


49
LG:215169.2:2000SEP08
7322496H1
156
636


49
LG:215169.2:2000SEP08
6314811H1
311
833


49
LG:215169.2:2000SEP08
g5664682
18
244


50
LG:410726.1:2000SEP08
2071327H1
360
550


50
LG:410726.1:2000SEP08
6912958J1
426
1019


50
LG:410726.1:2000SEP08
4583753H1
453
741


50
LG:410726.1:2000SEP08
7699696J1
724
1108


50
LG:410726.1:2000SEP08
207132716
751
1186


50
LG:410726.1:2000SEP08
g4176194
788
1231


50
LG:410726.1:2000SEP08
g3178308
806
1226


50
LG:410726.1:2000SEP08
g4149782
899
1217


50
LG:410726.1:2000SEP08
6912958H1
912
1382


50
LG:410726.1:2000SEP08
g3797002
1049
1163


50
LG:410726.1:2000SEP08
g3180193
1210
1289


50
LG:410726.1:2000SEP08
6534376H1
1
277


50
LG:410726.1:2000SEP08
6392976H1
1
276


50
LG:410726.1:2000SEP08
7233013H1
68
590


50
LG:410726.1:2000SEP08
6033171F6
69
623


50
LG:410726.1:2000SEP08
6033171H1
74
509


50
LG:410726.1:2000SEP08
g1648352
98
503


50
LG:410726.1:2000SEP08
3023715H1
259
523


50
LG:410726.1:2000SEP08
2071327F6
360
659


51
LG:234372.2:2000SEP08
1661362T6
2456
2794


51
LG:234372.2:2000SEP08
g2277847
2649
2848


51
LG:234372.2:2000SEP08
g3423969
2480
2842


51
LG:234372.2:2000SEP08
g2216700
2476
2633


51
LG:234372.2:2000SEP08
1550682R6
2348
2616


51
LG:234372.2:2000SEP08
g4243239
2398
2838


51
LG:234372.2:2000SEP08
5487834H1
2403
2668


51
LG:234372.2:2000SEP08
2097573H1
2418
2567


51
LG:234372.2:2000SEP08
g4535323
2421
2633


51
LG:234372.2:2000SEP08
g3840702
2425
2837


51
LG:234372.2:2000SEP08
266654216
2424
2800


51
LG:234372.2:2000SEP08
1537770H1
2437
2657


51
LG:234372.2:2000SEP08
1796389H1
2443
2647


51
LG:234372.2:2000SEP08
5065143H1
1951
2181


51
LG:234372.2:2000SEP08
3692831H1
1973
2248


51
LG:234372.2:2000SEP08
2436249H1
1989
2183


51
LG:234372.2:2000SEP08
3552362H1
1989
2135


51
LG:234372.2:2000SEP08
907632R2
2042
2608


51
LG:234372.2:2000SEP08
5024569H1
2057
2324


51
LG:234372.2:2000SEP08
35250769H1
2057
2298


51
LG:234372.2:2000SEP08
2689102H1
2087
2341


51
LG:234372.2:2000SEP08
3601859H1
2094
2400


51
LG:234372.2:2000SEP08
980210H1
2099
2420


51
LG:234372.2:2000SEP08
2683701H1
2101
2409


51
LG:234372.2:2000SEP08
1661356H1
2129
2344


51
LG:234372.2:2000SEP08
1661362H1
2129
2338


51
LG:234372.2:2000SEP08
1661362F6
2129
2473


51
LG:234372.2:2000SEP08
7751770J1
2137
2800


51
LG:234372.2:2000SEP08
184042416
2178
2800


51
LG:234372.2:2000SEP08
220074H1
2211
2385


51
LG:234372.2:2000SEP08
7348566H1
2237
2837


51
LG:234372.2:2000SEP08
6543746H1
2239
2820


51
LG:234372.2:2000SEP08
261600316
2249
2797


51
LG:234372.2:2000SEP08
6846460H1
2275
2812


51
LG:234372.2:2000SEP08
401177616
2286
2800


51
LG:234372.2:2000SEP08
7329765H1
2302
2789


51
LG:234372.2:2000SEP08
590936F1
2314
2837


51
LG:234372.2:2000SEP08
1511731T6
2317
2793


51
LG:234372.2:2000SEP08
5103857H1
2345
2565


51
LG:234372.2:2000SEP08
155068216
2348
2787


51
LG:234372.2:2000SEP08
1550682H1
2348
2558


51
LG:234372.2:2000SEP08
g1781803
1370
1603


51
LG:234372.2:2000SEP08
g883240
1432
1757


51
LG:234372.2:2000SEP08
971981R6
1447
1892


51
LG:234372.2:2000SEP08
971981H1
1447
1734


51
LG:234372.2:2000SEP08
600414H1
1450
1654


51
LG:234372.2:2000SEP08
4640503H1
1463
1733


51
LG:234372.2:2000SEP08
4096777H1
1476
1778


51
LG:234372.2:2000SEP08
7751770H1
1485
1986


51
LG:234372.2:2000SEP08
5799040H1
1483
1965


51
LG:234372.2:2000SEP08
4084077H1
1511
1780


51
LG:234372.2:2000SEP08
4650278H1
1546
1821


51
LG:234372.2:2000SEP08
2541227H1
1552
1796


51
LG:234372.2:2000SEP08
7653281H1
1556
2161


51
LG:234372.2:2000SEP08
2308666H1
1612
1801


51
LG:234372.2:2000SEP08
1719968F6
1614
2114


51
LG:234372.2:2000SEP08
1719968H1
1614
1837


51
LG:234372.2:2000SEP08
7322428H1
1727
2305


51
LG:234372.2:2000SEP08
g1646882
1750
2182


51
LG:234372.2:2000SEP08
4317152H1
1763
2035


51
LG:234372.2:2000SEP08
5301059F8
1776
2249


51
LG:234372.2:2000SEP08
7940028H1
1829
2452


51
LG:234372.2:2000SEP08
2666542F6
1854
2343


51
LG:234372.2:2000SEP08
2666542H1
1854
2099


51
LG:234372.2:2000SEP08
964975H1
1879
1991


51
LG:234372.2:2000SEP08
1381321H1
1890
2142


51
LG:234372.2:2000SEP08
5979524H1
1891
2177


51
LG:234372.2:2000SEP08
7060659H1
1895
2448


51
LG:234372.2:2000SEP08
2616003H1
799
1062


51
LG:234372.2:2000SEP08
2616003F6
799
1287


51
LG:234372.2:2000SEP08
7406896H1
837
1173


51
LG:234372.2:2000SEP08
3086412H1
861
1155


51
LG:234372.2:2000SEP08
6075203H1
879
1174


51
LG:234372.2:2000SEP08
7653281J1
888
1467


51
LG:234372.2:2000SEP08
5059222H1
1071
1336


51
LG:234372.2:2000SEP08
590936H1
1088
1346


51
LG:234372.2:2000SEP08
590970H1
1088
1209


51
LG:234372.2:2000SEP08
590936R1
1088
1612


51
LG:234372.2:2000SEP08
1317631H1
1091
1427


51
LG:234372.2:2000SEP08
3601816H1
1109
1413


51
LG:234372.2:2000SEP08
3529032H1
1114
1423


51
LG:234372.2:2000SEP08
3116380H1
1123
1407


51
LG:234372.2:2000SEP08
3117081H1
1124
1391


51
LG:234372.2:2000SEP08
4405926H1
1137
1397


51
LG:234372.2:2000SEP08
1511731F6
1143
1655


51
LG:234372.2:2000SEP08
2841541H1
1144
1399


51
LG:234372.2:2000SEP08
1511731H1
1143
1328


51
LG:234372.2:2000SEP08
1511356H1
1143
1327


51
LG:234372.2:2000SEP08
4056493H1
1302
1580


51
LG:234372.2:2000SEP08
g1959546
1304
1747


51
LG:234372.2:2000SEP08
g1349612
1328
1793


51
LG:234372.2:2000SEP08
g880451
1336
1792


51
LG:234372.2:2000SEP08
g830969
1336
1711


51
LG:234372.2:2000SEP08
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1336
1606


51
LG:234372.2:2000SEP08
5326001H2
1356
1608


51
LG:234372.2:2000SEP08
5325701H1
1356
1610


51
LG:234372.2:2000SEP08
1564961H1
1368
1557


51
LG:234372.2:2000SEP08
g2968054
2661
2838


51
LG:234372.2:2000SEP08
7033565H1
1
576


51
LG:234372.2:2000SEP08
4252317H1
46
191


51
LG:234372.2:2000SEP08
7171693H1
221
736


51
LG:234372.2:2000SEP08
7179847H1
221
651


51
LG:234372.2:2000SEP08
140734H1
240
341


51
LG:234372.2:2000SEP08
4938818H1
286
553


51
LG:234372.2:2000SEP08
7592182H1
465
1020


51
LG:234372.2:2000SEP08
1840424F6
478
838


51
LG:234372.2:2000SEP08
1840424H1
478
755


51
LG:234372.2:2000SEP08
4011776F6
494
963


51
LG:234372.2:2000SEP08
4011776H1
496
749


51
LG:234372.2:2000SEP08
2770053H1
556
809


51
LG:234372.2:2000SEP08
7759056H1
616
937


51
LG:234372.2:2000SEP08
4447071H1
636
912


51
LG:234372.2:2000SEP08
5373391H1
767
999


51
LG:234372.2:2000SEP08
1943237H1
2481
2735


51
LG:234372.2:2000SEP08
g2077756
2484
2840


51
LG:234372.2:2000SEP08
g883241
2495
2847


51
LG:234372.2:2000SEP08
g831477
2497
2849


51
LG:234372.2:2000SEP08
5301059T9
2527
2732


51
LG:234372.2:2000SEP08
g3700868
2531
2837


51
LG:234372.2:2000SEP08
g3872992
2532
2842


51
LG:234372.2:2000SEP08
971981T6
2531
2813


51
LG:234372.2:2000SEP08
5102936H1
2539
2791


51
LG:234372.2:2000SEP08
g1664296
2539
2633


51
LG:234372.2:2000SEP08
1292736H1
2564
2796


51
LG:234372.2:2000SEP08
3112301H1
2565
2851


51
LG:234372.2:2000SEP08
g4109330
2565
2633


51
LG:234372.2:2000SEP08
g2968055
2573
2838


51
LG:234372.2:2000SEP08
g49713A4
2598
2839


51
LG:234372.2:2000SEP08
2717958H1
2609
2837


51
LG:234372.2:2000SEP08
2766115H1
2752
2837


52
LG:022629.1:2000SEP08
3627874H1
253
538


52
LG:022629.1:2000SEP08
5786985H1
209
495


52
LG:022629.1:2000SEP08
3627896H1
242
449


52
LG:022629.1:2000SEP08
5403369H1
1
231


52
LG:022629.1:2000SEP08
540336919
337
738


52
LG:022629.1:2000SEP08
6082254H1
201
724


52
LG:022629.1:2000SEP08
g2198283
364
668


52
LG:022629.1:2000SEP08
5403369T8
192
649


52
LG:022629.1:2000SEP08
g3162701
219
638


52
LG:022629.1:2000SEP08
3627896F6
155
599


52
LG:022629.1:2000SEP08
5403369F8
19
594


52
LG:022629.1:2000SEP08
1519408H1
354
551


52
LG:022629.1:2000SEP08
1519416H1
354
541


52
LG:022629.1:2000SEP08
7683101H1
748
1276


52
LG:022629.1:2000SEP08
6569535H1
649
1171


52
LG:022629.1:2000SEP08
1519416T6
592
877


52
LG:022629.1:2000SEP08
5958910H1
759
865


52
LG:022629.1:2000SEP08
g6450919
360
843


52
LG:022629.1:2000SEP08
g6836892
618
843


52
LG:022629.1:2000SEP08
g4738617
377
842


52
LG:022629.1:2000SEP08
g4186678
404
842


52
LG:022629.1:2000SEP08
g5541594
602
840


52
LG:022629.1:2000SEP08
3627896T6
288
800


52
LG:022629.1:2000SEP08
1519416F6
354
771


52
LG:022629.1:2000SEP08
g2783063
400
762


52
LG:022629.1:2000SEP08
g2958447
367
762


52
LG:022629.1:2000SEP08
g2198251
454
762


52
LG:022629.1:2000SEP08
g2876399
393
762


53
LG:068682.1:2000SEP08 2011384H1
190
263


53
LG:068682.1:2000SEP08
g5438746
1
423


53
LG:068682.1:2000SEP08
g3805312
34
423


53
LG:068682.1:2000SEP08
g4372490
78
423


53
LG:068682.1:2000SEP08
g2954208
76
423


53
LG:068682.1:2000SEP08
g2954218
142
422


53
LG:068682.1:2000SEP08
g6838215
124
383


53
LG:068682.1:2000SEP08
g3307490
142
344


53
LG:068682.1:2000SEP08 6829315W
314
884


53
LG:068682.1:2000SEP08
g3109791
492
811


53
LG:068682.1:2000SEP08
g5452473
492
650


53
LG:068682.1:2000SEP08
g4564783
26
423


53
LG:068682.1:2000SEP08
g6043518
78
423


54
LG:222335.1:2000SEP08
6804715H1
612
1189


54
LG:222335.1:2000SEP08
2317449H1
764
853


54
LG:222335.1:2000SEP08
2583954F6
816
1189


54
LG:222335.1:2000SEP08
2583954H1
816
1087


54
LG:222335.1:2000SEP08
5591720H1
954
1099


54
LG:222335.1:2000SEP08
785266H1
1056
1206


54
LG:222335.1:2000SEP08
785266R6
1056
1423


54
LG:222335.1:2000SEP08
6336926H1
1134
1419


54
LG:222335.1:2000SEP08
6336926F8
1134
1420


54
LG:222335.1:2000SEP08
7063506H1
1
370


54
LG:222335.1:2000SEP08
3778951H1
1
282


54
LG:222335.1:2000SEP08
6258260H1
1
284


54
LG:222335.1:2000SEP08
5560479H1
7
218


54
LG:222335.1:2000SEP08
3113348H1
10
289


54
LG:222335.1:2000SEP08
702435H1
15
242


54
LG:222335.1:2000SEP08
4974222H1
18
276


54
LG:222335.1:2000SEP08
2343445H1
20
268


54
LG:222335.1:2000SEP08
2343445F6
20
546


54
LG:222335.1:2000SEP08
711988H1
85
306


54
LG:222335.1:2000SEP08
704169H1
85
364


54
LG:222335.1:2000SEP08
337408H1
93
282


54
LG:222335.1:2000SEP08
3163266H1
155
431


54
LG:222335.1:2000SEP08
4640786H1
165
437


54
LG:222335.1:2000SEP08
2343445T6
264
815


54
LG:222335.1:2000SEP08
439477H1
272
514


54
LG:222335.1:2000SEP08
3778951T6
332
830


54
LG:222335.1:2000SEP08
1737725F6
401
888


54
LG:222335.1:2000SEP08
1737725H1
401
608


54
LG:222335.1:2000SEP08
4001016H1
435
583


54
LG:222335.1:2000SEP08
g3841204
548
853


54
LG:222335.1:2000SEP08
6336726H1
1174
1420


54
LG:222335.1:2000SEP08
6850125H1
1178
1420


55
LG:331342.1:2000SEP08
3415969F7
497
980


55
LG:331342.1:2000SEP08
1003818H1
601
809


55
LG:331342.1:2000SEP08
7340365H1
601
1134


55
LG:331342.1:2000SEP08
4542316H1
633
873


55
LG:331342.1:2000SEP08
4542316F6
639
1203


55
LG:331342.1:2000SEP08
4519202H1
712
975


55
LG:331342.1:2000SEP08
1272054H1
899
1126


55
LG:331342.1:2000SEP08
3966023H1
915
1057


55
LG:331342.1:2000SEP08
5316380H1
376
591


55
LG:331342.1:2000SEP08
5316222H1
376
534


55
LG:331342.1:2000SEP08
4050724H1
457
746


55
LG:331342.1:2000SEP08
3415969H1
468
727


55
LG:331342.1:2000SEP08
2414808T6
1
201


55
LG:331342.1:2000SEP08
194403H1
3
176


55
LG:331342.1:2000SEP08
3962146F6
8
193


55
LG:331342.1:2000SEP08
2414808F6
8
441


55
LG:331342.1:2000SEP08
3962146H1
60
193


55
LG:331342.1:2000SEP08
2414808H1
191
441


55
LG:331342.1:2000SEP08
7637162H1
302
876


55
LG:331342.1:2000SEP08
6606050H1
312
789


55
LG:331342.1:2000SEP08
7312830H1
361
823


55
LG:331342.1:2000SEP08
5316167H1
376
584


55
LG:331342.1:2000SEP08
5318337H1
376
622


56
LG:021770.1:2000SEP08
5875430H1
597
866


56
LG:021770.1:2000SEP08
718539H1
656
941


56
LG:021770.1:2000SEP08
6553139T8
594
1115


56
LG:021770.1:2000SEP08
4618506H1
590
827


56
LG:021770.1:2000SEP08
7160062H1
453
950


56
LG:021770.1:2000SEP08
7603731J1
525
957


56
LG:021770.1:2000SEP08
3778516H1
433
735


56
LG:021770.1:2000SEP08
4819519H1
70
340


56
LG:021770.1:2000SEP08
4970514H1
341
610


56
LG:021770.1:2000SEP08
5686262F6
57
592


56
LG:021770.1:2000SEP08
g2155825
66
560


56
LG:021770.1:2000SEP08
4819519F7
69
652


56
LG:021770.1:2000SEP08
5754744H1
1
497


56
LG:021770.1:2000SEP08
5686262H1
43
299


56
LG:021770.1:2000SEP08
5068302H1
43
315


56
LG:021770.1:2000SEP08
g1442458
54
265


56
LG:021770.1:2000SEP08
2477611H1
858
1061


56
LG:021770.1:2000SEP08
2477611F7
858
1292


56
LG:021770.1:2000SEP08
2477611F6
858
1333


56
LG:021770.1:2000SEP08
4313608H1
871
1193


56
LG:021770.1:2000SEP08
1461091H1
899
1137


56
LG:021770.1:2000SEP08
639781H1
945
1212


56
LG:021770.1:2000SEP08
7619831J1
953
1308


56
LG:021770.1:2000SEP08
2477611T6
1011
1575


56
LG:021770.1:2000SEP08
1967278R6
1019
1507


56
LG:021770.1:2000SEP08
1967278H1
1020
1295


56
LG:021770.1:2000SEP08
243837H1
1071
1231


56
LG:021770.1:2000SEP08
1007489H1
1138
1433


56
LG:021770.1:2000SEP08
g6472352
1247
1618


56
LG:021770.1:2000SEP08
7396616H1
1261
1773


56
LG:021770.1:2000SEP08
g2155826
1268
1631


56
LG:021770.1:2000SEP08
g3116842
1287
1641


56
LG:021770.1:2000SEP08
g709667
1293
1623


56
LG:021770.1:2000SEP08
g2100629
1294
1624


56
LG:021770.1:2000SEP08
g816343
1352
1619


56
LG:021770.1:2000SEP08
g816686
1358
1619


56
LG:021770.1:2000SEP08
g670313
1362
1610


56
LG:021770.1:2000SEP08
g682772
1366
1610


56
LG:021770.1:2000SEP08
7756477J1
1399
1997


56
LG:021770.1:2000SEP08
2615849H1
1419
1605


56
LG:021770.1:2000SEP08
5259534H1
1463
1620


56
LG:021770.1:2000SEP08
g2719096
1552
1630


56
LG:021770.1:2000SEP08
3483806F6
1564
2025


56
LG:021770.1:2000SEP08
3483806H1
1564
1742


56
LG:021770.1:2000SEP08
3187717T6
1586
1971


56
LG:021770.1:2000SEP08
3352115H1
1659
1749


56
LG:021770.1:2000SEP08
1812178H1
1713
1979


56
LG:021770.1:2000SEP08
7756477H1
1781
2056


56
LG:021770.1:2000SEP08
5851722H1
1851
2056


56
LG:021770.1:2000SEP08
3187717R6
1876
2056


56
LG:021770.1:2000SEP08
1967278T6
1884
2471


56
LG:021770.1:2000SEP08
4187256H1
1909
2057


56
LG:021770.1:2000SEP08
4184364H1
1914
2132


56
LG:021770.1:2000SEP08
3483806T6
1931
2478


56
LG:021770.1:2000SEP08
7250489H1
1945
2497


56
LG:021770.1:2000SEP08
7250522H1
1945
2491


56
LG:021770.1:2000SEP08
5686262T6
1952
2470


56
LG:021770.1:2000SEP08
3187717H1
1983
2044


56
LG:021770.1:2000SEP08
2570543H1
2327
2515


56
LG:021770.1:2000SEP08
2570543R6
2327
2515


56
LG:021770.1:2000SEP08
2570543T6
2327
2477


56
LG:021770.1:2000SEP08
5958482H1
2341
2503


56
LG:021770.1:2000SEP08
1618155T6
2368
2477


56
LG:021770.1:2000SEP08
4692935H1
2368
2420


56
LG:021770.1:2000SEP08
g6470601
2368
2522


56
LG:021770.1:2000SEP08
1732834H1
2373
2450


56
LG:021770.1:2000SEP08
g2782960
2445
2581


56
LG:021770.1:2000SEP08
6100740H1
2452
2643


56
LG:021770.1:2000SEP08
3249668T6
2561
3105


56
LG:021770.1:2000SEP08
3249668F6
2813
3082


56
LG:021770.1:2000SEP08
3249668H1
2932
3082


57
LG:181607.9:2000SEP08
7344412H1
37
548


57
LG:181607.9:2000SEP08
7616670H1
40
579


57
LG:181607.9:2000SEP08
3382088H1
71
302


57
LG:181607.9:2000SEP08
3622354H1
71
323


57
LG:181607.9:2000SEP08
3810979H1
79
382


57
LG:181607.9:2000SEP08
6314189F8
80
762


57
LG:181607.9:2000SEP08
4763755H1
93
271


57
LG:181607.9:2000SEP08
g1317224
95
516


57
LG:181607.9:2000SEP08
2734055H1
105
366


57
LG:181607.9:2000SEP08
2986979H1
107
350


57
LG:181607.9:2000SEP08
g885028
221
484


57
LG:181607.9:2000SEP08
g885016
222
578


57
LG:181607.9:2000SEP08
3735039H1
266
504


57
LG:181607.9:2000SEP08
3199148H1
1
268


58
LG:1042768.1:2000SEP08
6798443H1
1
438


58
LG: 1042768.1:2000SEP08
6790795F8
1
602


58
LG:1042768.1:2000SEP08
6790795H1
1
529


58
LG:1042768.1:2000SEP08
6798443F8
1
618


58
LG: 1042768.1:2000SEP08
6790795T8
244
850


59
LG:282729.1:2000SEP08
4365538F6
1
292


59
LG:282729.1:2000SEP08
4365538H1
1
261


59
LG:282729.1:2000SEP08
6810113J1
11
398


59
LG:282729.1:2000SEP08
6810113H1 13
399


59
LG:282729.1:2000SEP08
5137624H1
248
353


59
LG:282729.1:2000SEP08
g4069212
253
704


59
LG:282729.1:2000SEP08
5137624T6
354
664


60
LG:998305.3:2000SEP08
3591650H1
1
282


60
LG:998305.3:2000SEP08
3651255H1
65
362


60
LG:998305.3:2000SEP08
3651255F6
66
617


60
LG:998305.3:2000SEP08
3462213H1
477
742


60
LG:998305.3:2000SEP08
3651 255T6
577
927


60
LG:998305.3:2000SEP08
1853882H1
669
803


60
LG:998305.3:2000SEP08
1854687H1
669
962


60
LG:998305.3:2000SEP08
1854687F6
669
956


60
LG:998305.3:2000SEP08
2244779H1
776
928


61
LG:1135213.1:2000SEP08
4145560H1
1
337


61
LG:1135213.1:2000SEP08
7182979H1
1
537


61
LG:1135213.1:2000SEP08
g4929686
1
1581


61
LG:1135213.1:2000SEP08
g1881193
113
359


61
LG:1135213.1:2000SEP08
798770H1
206
449


61
LG:1135213.1:2000SEP08
g1198695
214
498


61
LG:1135213.1:2000SEP08
g1637735
380
642


61
LG:1135213.1:2000SEP08
g2204679
39
511


61
LG:1135213.1:2000SEP08
5540595H1
1
195


61
LG:1135213.1:2000SEP08
g1970769
1
345


61
LG:1135213.1:2000SEP08
g1970753
1
325


61
LG:1135213.1:2000SEP08
g1971048
1
253


61
LG:I135213.1:2000SEP08
g1970777
1
223


61
LG:1135213.1:2000SEP08
g815792
8
284


61
LG:1135213.1:2000SEP08
g1441646
3
303


61
LG:1135213.1:2000SEP08
g4372035
14
479


61
LG:1135213.1:2000SEP08
g2930515
35
487


61
LG:1135213.1:2000SEP08
g4897951
44
477


61
LG:1135213.1:2000SEP08
609028H1
27
178


61
LG:1135213.1:2000SEP08
g2782816
15
417


61
LG:1135213.1:2000SEP08
g4326525
1
141


61
LG:1135213.1:2000SEP08
g2525795
28
236


62
LG:267762.1:2000SEP08
3941090F8
1
334


62
LG:267762.1:2000SEP08
1704531H1
153
292


62
LG:267762.1:2000SEP08
7658244J1
267
830


62
LG:267762.1:2000SEP08
5674936F6
283
888


62
LG:267762.1:2000SEP08
5674936H1
283
545


62
LG:267762.1:2000SEP08
5785070H1
482
768


62
LG:267762.1:2000SEP08
2831361H1
514
783


62
LG:267762.1:2000SEP08
g1523057
527
994


62
LG:267762.1:2000SEP08
6244881H1
600
677


62
LG:267762.1:2000SEP08
3731660H1
675
978


62
LG:267762.1:2000SEP08
g1950270
777
1103


62
LG:267762.1:2000SEP08
5674936T6
782
1313


62
LG:267762.1:2000SEP08
7762849J1
824
1474


62
LG:267762.1:2000SEP08
g1523013
882
1063


62
LG:267762.1:2000SEP08
g3678477
895
1352


62
LG:267762.1:2000SEP08
2797262H1
986
1231


62
LG:267762.1:2000SEP08
2797262F6
986
1555


62
LG:267762.1:2000SEP08
3732853H1
1059
1205


62
LG:267762.1:2000SEP08
g766967
1146
1503


62
LG:267762.1:2000SEP08
2797262T6
1199
1645


62
LG:267762.1:2000SEP08
6768646J1
1221
1437


62
LG:267762.1:2000SEP08
2561680H1
1367
1657


62
LG:267762.1:2000SEP08
g3750627
1401
1645


62
LG:267762.1:2000SEP08
g2557941
1510
1645


63
LG:120744.1:2000SEP08
5643301H1
1
266


63
LG:120744.1:2000SEP08
5643301F6
1
412


63
LG:120744.1:2000SEP08
7007819H1
12
557


63
LG:120744.1:2000SEP08
7161666H1
34
435


63
LG:120744.1:2000SEP08
7008530H1
19
463


63
LG:120744.1:2000SEP08
7161666F8
34
651


63
LG:120744.1:2000SEP08
7017571H1
42
211


63
LG:120744.1:2000SEP08
7017571F8
41
656


63
LG:120744.1:2000SEP08
3277305H1
128
393


63
LG:120744.1:2000SEP08
3277305F6
138
728


63
LG:120744.1:2000SEP08
3565182H1
492
782


63
LG:120744.1:2000SEP08
5643301R8
940
1116


63
LG:120744.1:2000SEP08
g4293857
672
947


63
LG:120744.1:2000SEP08
7161666R8
707
1169


63
LG:120744.1:2000SEP08
2992317H1
816
1098


63
LG:120744.1:2000SEP08
5643301R6
823
1115


64
LG:403409.1:2000SEP08
5643224H1
22
276


64
LG:403409.1:2000SEP08
91998848
22
296


64
LG:403409.1:2000SEP08
3126704H1
22
298


64
LG:403409.1:2000SEP08
3126978F6
22
611


64
LG:403409.1:2000SEP08
3126704F6
22
600


64
LG:403409.1:2000SEP08
3256088H1
24
259


64
LG:403409.1:2000SEP08
1728945H1
26
246


64
LG:403409.1:2000SEP08
6141236H1
28
370


64
LG:403409.1:2000SEP08
6141236F8
28
633


64
LG:403409.1:2000SEP08
6328822H1
47
592


64
LG:403409.1:2000SEP08
3388023H1
89
361


64
LG:403409.1:2000SEP08
6134014H1
110
401


64
LG:403409.1:2000SEP08
3323733H1
192
461


64
LG:403409.1:2000SEP08
3409854H1
357
618


64
LG:403409.1:2000SEP08
4068325F6
515
1108


64
LG:403409.1:2000SEP08
4068325H1
517
804


64
LG:403409.1:2000SEP08
3629455H1
560
835


64
LG:403409.1:2000SEP08
5499626H1
1
255


64
LG:403409.1:2000SEP08
5500026H1
1
161


64
LG:403409.1:2000SEP08
5500309H1
1
227


64
LG:403409.1:2000SEP08
5499909H1
1
206


64
LG:403409.1:2000SEP08
2723940H1
1
243


64
LG:403409.1:2000SEP08
2723940F6
1
333


64
LG:403409.1:2000SEP08
3751233H1
577
867


64
LG:403409.1:2000SEP08
5812189H1
644
840


64
LG:403409.1:2000SEP08
5812190H1
644
845


64
LG:403409.1:2000SEP08
311752H1
657
744


64
LG:403409.1:2000SEP08
373638H1
663
880


64
LG:403409.1:2000SEP08
7377730H1
697
1236


64
LG:403409.1:2000SEP08
6333709H1
705
1240


64
LG:403409.1:2000SEP08
6329688H1
705
1325


64
LG:403409.1:2000SEP08
7080559H1
760
1170


64
LG:403409.1:2000SEP08
6532643H1
803
1384


64
LG:403409.1:2000SEP08
g6570650
881
1310


64
LG:403409.1:2000SEP08
6141236T8
989
1579


64
LG:403409.1:2000SEP08
4068325T6
1018
1641


64
LG:403409.1:2000SEP08
3126704T6
1056
1580


64
LG:403409.1:2000SEP08
7068876H1
1069
1483


64
LG:403409.1:2000SEP08
3256362H1
1308
1554


64
LG:403409.1:2000SEP08
g1400213
1337
1682


64
LG:403409.1:2000SEP08
93254782
1346
1682


64
LG:403409.1:2000SEP08
g1383466
1395
1696


64
LG:403409.1:2000SEP08
6412487H1
1494
1931


64
LG:403409.1:2000SEP08
5534143H1
1578
1820


64
LG:403409.1:2000SEP08
7468129H1
1672
2123


64
LG:403409.1:2000SEP08
6869946H1
1717
2275


64
LG:403409.1:2000SEP08
g4510725
1831
2272


64
LG:403409.1:2000SEP08
6298042H1
1871
2146


64
LG:403409.1:2000SEP08
g1998847
1973
2275


64
LG:403409.1:2000SEP08
3541104H1
1991
2272


65
LG:226874.3:2000SEP08
6435270H1
1
397


65
LG:226874.3:2000SEP08
6431679H1
1
485


65
LG:226874.3:2000SEP08
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1
445


65
LG:226874.3:2000SEP08
6779705H1
178
713


65
LG:226874.3:2000SEP08
5767442F8
178
779


65
LG:226874.3:2000SEP08
5767442H1
316
780


65
LG:226874.3:2000SEP08
6779705R8
335
929


65
LG:226874.3:2000SEP08
6779705J1
335
933


65
LG:226874.3:2000SEP08
7198301H1
693
1099


65
LG:226874.3:2000SEP08
6536795H1
895
1461


65
LG:226874.3:2000SEP08
g2071279
927
1231


65
LG:226874.3:2000SEP08
g3802687
950
1338


65
LG:226874.3:2000SEP08
7264450H1
1077
1547


65
LG:226874.3:2000SEP08
6246443H1
1364
1871


66
LG:1045521.4:2000SEP08
g4453997
3410
3766


66
LG:1045521.4:2000SEP08
g5436696
3402
3773


66
LG:1045521.4:2000SEP08
g4266778
3401
3775


66
LG:1045521.4:2000SEP08
g3174193
3398
3774


66
LG:1045521.4:2000SEP08
4136385H1
3545
3829


66
LG:1045521.4:2000SEP08
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3607
3774


66
LG:1045521.4:2000SEP08
g4438434
3604
3773


66
LG:1045521.4:2000SEP08
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3394
3775


66
LG:1045521.4:2000SEP08
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3397
3777


66
LG:1045521.4:2000SEP08
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3369
3598


66
LG:1045521.4:2000SEP08
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3378
3641


66
LG:1045521.4:2000SEP08
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3380
3775


66
LG:1045521.4:2000SEP08
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3385
3679


66
LG:1045521.4:2000SEP08
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3390
3636


66
LG:1045521.4:2000SEP08
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3338
3766


66
LG:1045521.4:2000SEP08
7247994H1
3343
3773


66
LG:1045521.4:2000SEP08
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3345
3775


66
LG:1045521.4:2000SEP08
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3351
3775


66
LG:1045521.4:2000SEP08
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3350
3775


66
LG:1045521.4:2000SEP08
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3351
3776


66
LG:1045521.4:2000SEP08
g4394054
3354
3773


66
LG:1045521.4:2000SEP08
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3363
3775


66
LG:1045521.4:2000SEP08
2112746T6
3317
3735


66
LG:1045521.4:2000SEP08
1813318T6
3319
3739


66
LG:1045521.4:2000SEP08
g5673655
3323
3775


66
LG:1045521.4:2000SEP08
1813318F6
3326
3657


66
LG:1045521.4:2000SEP08
1813318H1
3326
3558


66
LG:1045521.4:2000SEP08
g4309999
3332
3776


66
LG:1045521.4:2000SEP08
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3338
3781


66
LG:1045521.4:2000SEP08
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3465
3787


66
LG:1045521.4:2000SEP08
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3478
3773


66
LG:1045521.4:2000SEP08
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3413
3734


66
LG:1045521.4:2000SEP08
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3415
3778


66
LG:1045521.4:2000SEP08
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3415
3775


66
LG:1045521.4:2000SEP08
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3414
3773


66
LG:1045521.4:2000SEP08
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3414
3775


66
LG:1045521.4:2000SEP08
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3415
3776


66
LG:1045521.4:2000SEP08
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3416
3775


66
LG:1045521.4:2000SEP08
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3417
3777


66
LG:1045521.4:2000SEP08
g2264833
3419
3775


66
LG:1045521.4:2000SEP08
g5152477
3424
3753


66
LG:1045521.4:2000SEP08
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3450
3682


66
LG:1045521.4:2000SEP08
3016423H1
3453
3753


66
LG:1045521.4:2000SEP08
g6474480
3316
3775


66
LG:1045521.4:2000SEP08
7705621H1
1924
2521


66
LG:1045521.4:2000SEP08
1287084H1
3313
3446


66
LG:1045521.4:2000SEP08
7022070H1
564
1144


66
LG:1045521.4:2000SEP08
g5444114
3311
3775


66
LG:1045521.4:2000SEP08
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3307
3778


66
LG:1045521.4:2000SEP08
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3312
3734


66
LG:1045521.4:2000SEP08
1287084F1
3313
3780


66
LG:1045521.4:2000SEP08
1757131H1
3095
3314


66
LG:1045521.4:2000SEP08
3121994H1
3121
3398


66
LG:1045521.4:2000SEP08
2681674H1
3126
3419


66
LG:1045521.4:2000SEP08
1710178H1
3140
3328


66
LG:1045521.4:2000SEP08
2706109T6
3161
3735


66
LG:1045521.4:2000SEP08
2607376T6
3175
3735


66
LG:1045521.4:2000SEP08
1398469H1
3181
3415


66
LG:1045521.4:2000SEP08
1686019T6
3196
3736


66
LG:1045521.4:2000SEP08
2480005H1
3202
3457


66
LG:1045521.4:2000SEP08
2480053H1
3202
3471


66
LG:1045521.4:2000SEP08
1414724H1
3219
3452


66
LG:1045521.4:2000SEP08
3966031H1
3221
3365


66
LG:1045521.4:2000SEP08
3965562H1
3221
3511


66
LG:1045521.4:2000SEP08
2419122T6
3256
3736


66
LG:1045521.4:2000SEP08
6315349H1
3283
3774


66
LG:1045521.4:2000SEP08
6315249H1
3283
3773


66
LG:1045521.4:2000SEP08
1863643T6
3285
3720


66
LG:1045521.4:2000SEP08
g3152117
3298
3778


66
LG:1045521.4:2000SEP08
7390568H2
2944
3392


66
LG:1045521.4:2000SEP08
7746832H1
2160
2715


66
LG:1045521.4:2000SEP08
7712386J1
1330
1972


66
LG:1045521.4:2000SEP08
7433684H1
176
707


66
LG:1045521.4:2000SEP08
5100939H1
3264
3502


66
LG:1045521.4:2000SEP08
g2291354
3519
3778


66
LG:1045521.4:2000SEP08
g4685761
3523
3782


66
LG:1045521.4:2000SEP08
g6703923
3374
3775


66
LG:1045521.4:2000SEP08
741995H1
3321
3564


66
LG:1045521.4:2000SEP08
g1349221
3264
3574


66
LG:1045521.4:2000SEP08
4731668H1
3257
3328


66
LG:1Q45521.4:2000SEP08
6256785H1
2960
3168


66
LG:1045521.4:2000SEP08
6892739H1
2973
3373


66
LG:1045521,4:2000SEP08
3016905H1
3022
3315


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LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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1801
2030


66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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2167


66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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2031
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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1919


66
LG:1045521.4:2000SEP08
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1919


66
LG:1045521.4:2000SEP08
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1920


66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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677
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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1
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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1
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66
LG:1045521.4:2000SEP08
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LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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455


66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08 6996631H1
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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177
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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287
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66
LG:1045521.4:2000SEP08
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330
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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66
LG:1045521.4:2000SEP08
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67
LG:275876.1:2000SEP08
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67
LG:275876.1:2000SEP08
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1
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67
LG:275876.1:2000SEP08
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67
LG:275876.1:2000SEP08
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67
LG:275876.1:2000SEP08
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263
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68
LG:475127.7:2000SEP08
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68
LG:475127.7:2000SEP08
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68
LG:475127.7:2000SEP08
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69
LG:157263.1:2000SEP08
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69
LG:157263.1:2000SEP08
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69
LG:157263.1:2000SEP08
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69
LG:157263.1:2000SEP08
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406
716


69
LG:157263.1:2000SEP08
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475
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69
LG:157263.1:2000SEP08
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69
LG:157263.1:2000SEP08
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69
LG:157263.1:2000SEP08
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69
LG:157263.1:2000SEP08
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958
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70
LG:247382.7:2000SEP08
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1
192


70
LG:247382.7:2000SEP08
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70
LG:247382.7:2000SEP08
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515


70
LG:247382.7:2000SEP08
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70
LG:247382.7:2000SEP08
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70
LG:247382.7:2000SEP08
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70
LG:247382.7:2000SEP08
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70
LG:247382.7:2000SEP08
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70
LG:247382.7:2000SEP08
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70
LG:247382.7:2000SEP08
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70
LG:247382.7:2000SEP08
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70
LG:247382.7:2000SEP08
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70
LG:247382.7:2000SEP08
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70
LG:247382.7:2000SEP08
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70
LG:247382.7:2000SEP08
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70
LG:247382.7:2000SEP08
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550
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70
LG:247382.7:2000SEP08
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70
LG:247382.7:2000SEP08
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LG:247382.7:2000SEP08
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LG:247382.7:2000SEP08
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LG:247382.7:2000SEP08
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LG:247382.7:2000SEP08
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70
LG:247382.7:2000SEP08
5090313H1
327
559


70
LG:247382.7:2000SEP08
5047038F6
362
983


70
LG:247382.7:2000SEP08
5047038H1
364
646


70
LG:247382.7:2000SEP08
701 3633H1
482
764


71
LG:197367.5:2000SEP08
6032665H1
1
569


72
LG:218090.5:2000SEP08
g4970262
554
899


72
LG:218090.5:2000SEP08
7619489H1
1
594


72
LG:218090.5:2000SEP08
5218316H1
34
271


72
LG:218090.5:2000SEP08
g5838654
37
288


73
LG:216612.4:2000SEP08
6927865H1
598
1049


73
LG:216612.4:2000SEP08
6765038H1
1
356


73
LG:216612.4:2000SEP08
6823189H1
1
515


73
LG:216612.4:2000SEP08
6823189J1
268
821


73
LG:216612.4:2000SEP08
4699496F7
688
1261


73
LG:216612.4:2000SEP08
4699496H1
688
891


73
LG:216612.4:2000SEP08
6126235F6
1004
1666


73
LG:216612.4:2000SEP08
6118801H1
1004
1129


73
LG:216612.4:2000SEP08
g1012738
705
946


73
LG:216612.4:2000SEP08
7719209J1
752
1298


73
LG:216612.4:2000SEP08
7744047H1
782
1296


73
LG:216612.4:2000SEP08
g794554
2469
2740


73
LG:216612.4:2000SEP08
5905071F8
2017
2563


73
LG:216612.4:2000SEP08
5905071F6
2022
2389


73
LG:216612.4:2000SEP08
5905071H1
2022
2292


73
LG:216612.4:2000SEP08
5905071T9
2037
2624


73
LG:216612.4:2000SEP08
7744047J1
2120
2706


73
LG:216612.4:2000SEP08
g562707
2447
2728


73
LG:216612.4:2000SEP08
g764767
1368
1693


73
LG:216612.4:2000SEP08
7719209H1
1382
1940


73
LG:216612.4:2000SEP08
6765038J1
1574
2159


73
LG:216612.4:2000SEP08
g1012737
1627
1867


73
LG:216612.4:2000SEP08
5905171H1
2013
2278


73
LG:216612.4:2000SEP08
6126235H1
1004
1556


73
LG:216612.4:2000SEP08
4699496T7
1179
1651


73
LG:216612.4:2000SEP08
g572752
1367
1734


74
LG:197614.1:2000SEP08
1287527H1
3708
3958


74
LG:197614.1:2000SEP08
2286805H1
3713
3944


74
LG:197614.1:2000SEP08
g1165770
3724
3845


74
LG:197614.1:2000SEP08
2169536H1
3730
3980


74
LG:197614.1:2000SEP08
3452306H1
3730
3894


74
LG:197614.1:2000SEP08
628239H1
3750
4013


74
LG:197614.1:2000SEP08
5306905H1
3778
3895


74
LG:197614.1:2000SEP08
5757045H1
3806
4001


74
LG:197614.1:2000SEP08
1287527F1
3708
4248


74
LG:197614.1:2000SEP08
5898662H1
3622
3910


74
LG:197614.1:2000SEP08
5895501H1
3623
3920


74
LG:197614.1:2000SEP08
g2140565
3623
3950


74
LG:197614.1:2000SEP08
5730757H1
3622
3823


74
LG:197614.1:2000SEP08
1544877H1
3671
3870


74
LG:197614.1:2000SEP08
5271113H1
3701
3950


74
LG:197614.1:2000SEP08
6085421H1
3704
4135


74
LG:197614.1:2000SEP08
g1933869
3703
3944


74
LG:197614.1:2000SEP08
g2899129
2999
3411


74
LG:197614.1:2000SEP08
g5425670
3002
3466


74
LG:197614.1:2000SEP08
3449642H1
3016
3248


74
LG:197614.1:2000SEP08
g5812471
54
465


74
LG:197614.1:2000SEP08
5914544H1
767
939


74
LG:197614.1:2000SEP08
3105863H1
146
423


74
LG:197614.1:2000SEP08
3270954H1
150
283


74
LG:197614.1:2000SEP08
g4899736
204
582


74
LG:197614.1:2000SEP08
g4153549
211
637


74
LG:197614.1:2000SEP08
g5849305
214
637


74
LG:197614.1:2000SEP08
g1815090
228
641


74
LG:197614.1:2000SEP08
g4899744
250
581


74
LG:197614.1:2000SEP08
g1624602
340
638


74
LG:197614.1:2000SEP08
g734108
416
607


74
LG:197614.1:2000SEP08
6608771H1
573
1078


74
LG:197614.1:2000SEP08
7467077H1
692
1231


74
LG:197614.1:2000SEP08
g2620587
4369
4614


74
LG:197614.1:2000SEP08
g777201
4372
4614


74
LG:197614.1:2000SEP08
g4523723
4378
4613


74
LG:197614.1:2000SEP08
5161106H1
4398
4607


74
LG:197614.1:2000SEP08
3690612H1
4464
4758


74
LG:197614.1:2000SEP08
3702535H1
4476
4613


74
LG:197614.1:2000SEP08
661314T6
4484
4570


74
LG:197614.1:2000SEP08
1929304H1
4529
4768


74
LG:197614.1:2000SEP08
1929304F6
4529
4748


74
LG:197614.1:2000SEP08
3010805H1
4578
4864


74
LG:197614.1:2000SEP08
g6661262
1
472


74
LG:197614.1:2000SEP08
g3401176
1
445


74
LG:197614.1:2000SEP08
g5637467
1
499


74
LG:197614.1:2000SEP08
g5755549
1
448


74
LG:197614.1:2000SEP08
g1614502
1
480


74
LG:197614.1:2000SEP08
6763231J1
11
86


74
LG:197614.1:2000SEP08
g4305963
23
478


74
LG:197614.1:2000SEP08
g3232676
24
468


74
LG:197614.1:2000SEP08
g6713108
33
494


74
LG:197614.1:2000SEP08
g4888325
42
466


74
LG:197614.1:2000SEP08
g2910679
34
458


74
LG:197614.1:2000SEP08
g5635762
49
399


74
LG:197614.1:2000SEP08
564653H1
4227
4440


74
LG:197614.1:2000SEP08
4827983H1
4317
4583


74
LG:197614.1:2000SEP08
g2877107
4324
4617


74
LG:197614.1:2000SEP08
2504732H1
4228
4450


74
LG:197614.1:2000SEP08
3525080H1
4231
4496


74
LG:197614.1:2000SEP08
2296610H1
4241
4501


74
LG:197614.1:2000SEP08
704337H1
4258
4476


74
LG:197614.1:2000SEP08
6736875H1
4259
4602


74
LG:197614.1:2000SEP08
1638150T6
4295
4578


74
LG:197614.1:2000SEP08
4615882H1
4316
4570


74
LG:197614.1:2000SEP08
1358968H1
4365
4605


74
LG:197614.1:2000SEP08
1916409H1
3605
3856


74
LG:197614.1:2000SEP08
180009R6
3093
3516


74
LG:197614.1:2000SEP08
180009H1
3093
3275


74
LG:197614.1:2000SEP08
g1490176
3095
3467


74
LG:197614.1:2000SEP08
3117564H1
3095
3392


74
LG:197614.1:2000SEP08
g2902729
3096
3466


74
LG:197614.1:2000SEP08
4523772H1
3108
3352


74
LG:197614.1:2000SEP08
g3841726
3126
3467


74
LG:197614.1:2000SEP08
g1492261
3133
3467


74
LG:197614.1:2000SEP08
5334175H1
3146
3312


74
LG:197614.1:2000SEP08
463918H1
3146
3386


74
LG:197614.1:2000SEP08
g1886770
3148
3439


74
LG:197614.1:2000SEP08
1453577F6
3179
3472


74
LG:197614.1:2000SEP08
1452163H1
3179
3432


74
LG:197614.1:2000SEP08
1452163F1
3179
3649


74
LG:197614.1:2000SEP08
1453577H1
3179
3432


74
LG:197614.1:2000SEP08
g1635322
3203
3378


74
LG:197614.1:2000SEP08
4883761H1
3218
3425


74
LG:197614.1:2000SEP08
g4534089
3221
3467


74
LG:197614.1:2000SEP08
5873648H1
3289
3537


74
LG:197614.1:2000SEP08
7132968H1
3304
3749


74
LG:197614.1:2000SEP08
3516403H1
3312
3559


74
LG:197614.1:2000SEP08
4261 15T6
3327
3789


74
LG:197614.1:2000SEP08
5664838H1
3325
3613


74
LG:197614.1:20003EP08
3514295H1
3364
3619


74
LG:197614.1:2000SEP08
2568145H1
3378
3627


74
LG:197614.1:2000SEP08
2569762H1
3378
3633


74
LG:197614.1:20003EP08
4898290H1
3614
3884


74
LG:197614.1:2000SEP08
g2047002
3401
3794


74
LG:197614.1:2000SEP08
g2047020
3401
3744


74
LG:197614.1:2000SEP08
7137103H1
3618
3749


74
LG:197614.1:2000SEP08
6608771T1
3442
3878


74
LG:197614.1:2000SEP08
6875871H1
3442
3973


74
LG:197614.1:2000SEP08
060722H1
3479
3591


74
LG:197614.1:2000SEP08
5833944H1
3484
3743


74
LG:197614.1:2000SEP08
g2838778
3504
3964


74
LG:197614.1:2000SEP08
1668733T6
3509
3907


74
LG:197614.1:2000SEP08
g4285920
3515
3949


74
LG:197614.1:2000SEP08
1668733F6
3516
3890


74
LG:197614.1:2000SEP08
1668733H1
3516
3739


74
LG:197614.1:2000SEP08
5301951H1
3528
3739


74
LG:197614.1:2000SEP08
g6946407
3543
3948


74
LG:197614.1:2000SEP08
g2140557
3549
3950


74
LG:197614.1:2000SEP08
871967R1
3572
3994


74
LG:197614.1:2000SEP08
871967H1
3573
3812


74
LG:197614.1:2000SEP08
3510984H1
3603
3826


74
LG:197614.1:2000SEP08
2041903H1
3602
3769


74
LG:197614.1:2000SEP08
5904560H1
3622
3920


74
LG:197614.1:2000SEP08
g5444559
4204
4615


74
LG:197614.1:2000SEP08
g2820548
4204
4613


74
LG:197614.1:2000SEP08
g4896092
4204
4606


74
LG:197614.1:2000SEP08
g5447131
4204
4613


74
LG:197614.1:2000SEP08
1638150H1
4204
4351


74
LG:197614.1:2000SEP08
701181H1
4204
4370


74
LG:197614.1:2000SEP08
g2563289
4206
4577


74
LG:197614.1:2000SEP08
2437436H1
4221
4443


74
LG:197614.1:2000SEP08
1638150F6
4204
4545


74
LG:197614.1:2000SEP08
426115H1
2948
3152


74
LG:197614.1:2000SEP08
g5528772
2988
3466


74
LG:197614.1:2000SEP08
1581709H1
4096
4291


74
LG:197614.1:2000SEP08
1581803H1
4096
4307


74
LG:197614.1:2000SEP08
5652453H1
4108
4614


74
LG:197614.1:2000SEP08
5732485T6
4093
4566


74
LG:197614.1:2000SEP08
1581784H1
4096
4291


74
LG:197614.1:2000SEP08
g4739964
4187
4609


74
LG:197614.1:2000SEP08
g3898531
4197
4614


74
LG:197614.1:2000SEP08
g4243541
4197
4614


74
LG:197614.1:2000SEP08
g6397736
4203
4615


74
LG:197614.1:2000SEP08
5809075H2
2712
2950


74
LG:197614.1:2000SEP08
660019H1
2845
3116


74
LG:197614.1:2000SEP08
7070142H1
2718
3259


74
LG:197614.1:2000SEP08
g4896323
2733
3113


74
LG:197614.1:2000SEP08
661314H1
2845
3130


74
LG:197614.1:2000SEP08
661314R6
2845
3187


74
LG:197614.1:2000SEP08
g1933868
2740
3080


74
LG:197614.1:2000SEP08
6025513H1
2853
3151


74
LG:197614.1:2000SEP08
6931975H1
2747
3260


74
LG:197614.1:2000SEP08
g1886879
2748
3105


74
LG:197614.1:2000SEP08
3570587H1
2804
3083


74
LG:197614.1:2000SEP08
6197889H1
2815
3281


74
LG:197614.1:2000SEP08
6202948H1
2817
3392


74
LG:197614.1:2000SEP08
g1491312
2821
3260


74
LG:197614.1:2000SEP08
7664971H1
2823
3356


74
LG:197614.1:2000SEP08
660648H1
2845
3118


74
LG:197614.1:2000SEP08
g1989594
2864
3024


74
LG:197614.1:2000SEP08
378504H1
2428
2614


74
LG:197614.1:2000SEP08
378504R6
2428
2929


74
LG:197614.1:2000SEP08
5834173H1
2474
2744


74
LG:197614.1:2000SEP08
5391905H1
2515
2792


74
LG:197614.1:2000SEP08
2534074H1
2628
2875


74
LG:197614.1:2000SEP08
6951984H1
2643
3252


74
LG:197614.1:2000SEP08
7621265H1
2095
2621


74
LG:197614.1:2000SEP08
5729256H1
2254
2747


74
LG:197614.1:2000SEP08
7439141H1
2355
2829


74
LG:197614.1:2000SEP08
g1747961
2280
2586


74
LG:197614.1:2000SEP08
5349468H1
2351
2584


74
LG:197614.1:2000SEP08
6763231H1
2374
2905


74
LG:197614.1:2000SEP08
7650036H2
2417
2975


74
LG:197614.1:2000SEP08
7156980H1
938
1507


74
LG:197614.1:2000SEP08
7663421H1
1134
1649


74
LG:197614.1:2000SEP08
7650036J2
1157
1772


74
LG:197614.1:2000SEP08
7359954H1
1252
1784


74
LG:197614.1:2000SEP08
7621265J1
1262
1833


74
LG:197614.1:2000SEP08
5732485H1
1126
1318


74
LG:197614.1:2000SEP08
7080048H1
1640
2223


74
LG:197614.1:2000SEP08
6485720H1
1880
2304


74
LG:197614.1:2000SEP08
6485720F9
1926
2075


74
LG:197614.1:2000SEP08
081459H1
1973
2232


74
LG:197614.1:2000SEP08
7663421J1
2044
2608


74
LG:197614.1:2000SEP08
g3423345
3018
3467


74
LG:197614.1:2000SEP08
g5590054
3020
3467


74
LG:197614.1:2000SEP08
g4111681
3027
3467


74
LG:197614.1:2000SEP08
2617018H2
3029
3265


74
LG:197614.1:2000SEP08
3815347H1
3033
3315


74
LG:197614.1:2000SEP08
g777251
3046
3330


74
LG:197614.1:2000SEP08
g2817792
3086
3475


74
LG:197614.1:2000SEP08
4897664H1
3826
3991


74
LG:197614.1:2000SEP08
4896259H1
3849
4001


74
LG:197614.1:2000SEP08
g1212198
3850
4178


74
LG:197614.1:2000SEP08
g1748459
3880
3967


74
LG:197614.1:2000SEP08
5063386H1
3886
4001


74
LG:197614.1:2000SEP08
1491069H1
3900
4105


74
LG:197614.1:2000SEP08
1491069F6
3900
4001


74
LG:197614.1:2000SEP08
g896855
4022
4245


74
LG:197614.1:2000SEP08
g4901112
4022
4378


74
LG:197614.1:2000SEP08
g4990162
4025
4297


74
LG:197614.1:2000SEP08
96699628
4025
4483


74
LG:197614.1:2000SEP08
180009T6
4072
4569


74
LG:197614.1:2000SEP08
1491069T6
4075
4576


74
LG:197614.1:2000SEP08
6208837H1
4088
4388


74
LG:197614.1:2000SEP08
7355849H1
4097
4587


74
LG:197614.1:2000SEP08
2588654H1
2874
3132


74
LG:197614.1:2000SEP08
4261 15R6
2948
3453


74
LG:197614.1:2000SEP08
g1492260
2879
3120


74
LG:197614.1:2000SEP08
3873481H1
2937
3214


74
LG:197614.1:2000SEP08
425031H1
2948
3210


75
LG:378428.1:2000SEP08
6910888F8
560
708


75
LG:378428.1:2000SEP08
7379444H1
36
599


75
LG:378428.1:2000SEP08
6816543H1
185
640


75
LG:378428.1:2000SEP08
6816543F8
285
641


75
LG:378428.1:2000SEP08
7429391H1
439
956


75
LG:378428.1:2000SEP08
6816543R8
1
644


75
LG:378428.1:2000SEP08
7379418H1
36
609


75
LG:378428.1:2000SEP08
6910888J1
768
1376


75
LG:378428.1:2000SEP08
6910888R8
773
1449


75
LG:378428.1:2000SEP08
6044422H1
726
1023


75
LG:378428.1:2000SEP08
6044422F8
725
1341


75
LG:378428.1:2000SEP08
6755205H 1
598
1201


75
LG:378428.1:2000SEP08
54971 13R8
1551
2088


75
LG:378428.1:2000SEP08
54971 13R9
1559
2088


75
LG:378428.1:2000SEP08
5497113H1
1559
1823


75
LG:378428.1:2000SEP08
6044422R8
1304
1879


75
LG:378428.1:2000SEP08
4401305H1
1232
1481


75
LG:378428.1:2000SEP08
6044422J1
1416
1879


75
LG:378428.1:2000SEP08
6910888H1
1537
2074


75
LG:378428.1:2000SEP08
4401305F6
1232
1757


75
LG:378428.1:2000SEP08
5045827F6
1029
1501


75
LG:378428.1:2000SEP08
5045827H1
1029
1306


75
LG:378428.1:2000SEP08
7004756H1
1060
1494


75
LG:378428.1:2000SEP08
7010551H1
1639
2000


75
LG:378428.1:2000SEP08
5497113F9
1565
2088


75
LG:378428.1:2000SEP08
g2789298
2012
2404


75
LG:378428.1:2000SEP08
4401305T6
2011
2370


75
LG:378428.1:2000SEP08
g2006832
2112
2414


75
LG:378428.1:2000SEP08
g6713687
1969
2395


75
LG:378428.1:2000SEP08
g2912647
1982
2398


76
LG:286639.1:2000SEP08
5508394F6
681
1107


76
LG:286639.1:2000SEP08
5508394H1
681
881


76
LG:286639.1:2000SEP08
7687060J1
370
955


76
LG:286639.1:2000SEP08
3217093F6
740
1174


76
LG:286639.1:2000SEP08
3217093H1
740
1012


76
LG:286639.1:2000SEP08
g2025699
726
1059


76
LG:286639.1:2000SEP08
301366H1
1211
1426


76
LG:286639.1:2000SEP08
301366T6
1244
1768


76
LG:286639.1:2000SEP08
3217093T6
1309
1844


76
LG:286639.1:2000SEP08
5832442H1
1196
1448


76
LG:286639.1:2000SEP08
301366R6
1211
1672


76
LG:286639.1:2000SEP08
5507629H1
1181
1464


76
LG:286639.1:2000SEP08
7687060H1
1024
1612


76
LG:286639.1:20003EP08
4919304F6
1115
1523


76
LG:286639.1:2000SEP08
g3933409
1495
1975


76
LG:286639.1:2000SEP08
4919304H1
1392
1523


76
LG:286639.1:2000SEP08
g2057022
1460
1800


76
LG:286639.1:2000SEP08
6178302H1
1387
1560


76
LG:286639.1:2000SEP08
4249162F6
1965
2347


76
LG:286639.1:2000SEP08
g4739468
1906
2281


76
LG:286639.1:2000SEP08
g5812196
1867
1966


76
LG:286639.1:2000SEP08
g5397776
1881
2281


76
LG:286639.1:2000SEP08
g4739487
1904
2281


76
LG:286639.1:2000SEP08
g3446647
1519
1975


76
LG:286639.1:2000SEP08
5508394R6
1790
2257


76
LG:286639.1:2000SEP08
4249162H1
1965
2115


76
LG:286639.1:2000SEP08
g3109536
2091
2281


76
LG:286639.1:2000SEP08
95446112
2092
2281


76
LG:286639.1:2000SEP08
g6569543
1 466


76
LG:286639.1:2000SEP08
4138803H1
17
304


76
LG:286639.1:2000SEP08
3595464H1344
623


77
LG:389870.1:2000SEP08
7065623H1
534
764


77
LG:389870.1:2000SEP08
7191788H2
368
640


77
LG:389870.1:2000SEP08
7354238H1
129
677


77
LG:389870.1:2000SEP08
g2740716
1
454


77
LG:389870.1:2000SEP08
g4389793
1
454


77
LG:389870.1:2000SEP08
7459406H1
769
1222


77
LG:389870.1:2000SEP08
4030167H1
620
850


77
LG:389870.1:2000SEP08
7583301H1
710
1249


78
LG:1387485.6:2000SEP08
1259442F6
727
1286


78
LG:1387485.6:2000SEP08
575641H1
210
423


78
LG:1387485.6:2000SEP08
2695041H1
441
744


78
LG:1387485.6:2000SEP08
5394337H1
572
857


78
LG:1387485.6:2000SEP08
4773576H1
617
849


78
LG:1387485.6:2000SEP08
1722977H1
707
964


78
LG:1387485.6:2000SEP08
1722977F6
707
1113


78
LG:1387485.6:2000SEP08
1259442H1
726
966


78
LG:1387485.6:2000SEP08
5004203H 1
894
1024


78
LG:1387485.6:2000SEP08
4545090H1
897
1175


78
LG:1387485.6:2000SEP08
29441 36F6
907
1283


78
LG:1387485.6:2000SEP08
2944136H1
907
1198


78
LG:1387485.6:2000SEP08
3495979H1
912
1194


78
LG:1387485.6:2000SEP08
g1202624
939
1381


78
LG:1387485.6:2000SEP08
g1012265
955
1249


78
LG:1387485.6:2000SEP08
g1042452
956
1258


78
LG:1387485.6:2000SEP08
g983177
962
1336


78
LG:1387485.6:2000SEP08
3049691H1
963
1254


78
LG:1387485.6:2000SEP08
g1218110
1001
1269


78
LG:1387485.6:2000SEP08
2652533H1
1016
1269


78
LG:1387485.6:2000SEP08
2098947H1
1224
1456


78
LG:1387485.6:2000SEP08
1309581H1
1328
1575


78
LG:1387485.6:2000SEP08
1004812H1
1367
1552


78
LG:1387485.6:2000SEP08
1568541H1
1392
1607


78
LG:1387485.6:2000SEP08
2764023H1
1
259


78
LG:1387485.6:2000SEP08
530901H1
2
134


78
LG:1387485.6:2000SEP08
4049678H1
11
290


78
LG:1387485.6:2000SEP08
3594169H1
11
279


78
LG:1387485.6:2000SEP08
4330447H1
17
271


78
LG:1387485.6:2000SEP08
4565262H 1
39
285


78
LG:1387485.6:2000SEP08
6408733H 1
162
683


78
LG:1387485.6:2000SEP08
g1295497
175
615


78
LG:1387485.6:2000SEP08
7039706H1
356
875


78
LG:1387485.6:2000SEP08
986902H1
225
462


78
LG:1387485.6:2000SEP08
7939046H1
446
921


78
LG:1387485.6:2000SEP08
7270571H1
206
743


78
LG:1387485.6:2000SEP08
1704717H1
255
425


78
LG:1387485.6:2000SEP08
4723677H1
207
436


79
LG:230151.1:2000SEP08
g1760799
1489
1929


79
LG:230151.1:2000SEP08
2834338F6
1524
2017


79
LG:230151.1:2000SEP08
2588088F6
1290
1516


79
LG:230151.1:2000SEP08
2588088H1
1290
1533


79
LG:230151.1:2000SEP08
5562138H1
275
408


79
LG:230151.1:2000SEP08
7387281H1
281
540


79
LG:230151.1:2000SEP08
g1678023
294
403


79
LG:230151.1:2000SEP08
7625371H1
303
939


79
LG:230151.1:2000SEP08
g5037659
2811
2935


79
LG:230151.1:2000SEP08
g4094483
2814
2935


79
LG:230151.1:2000SEP08
4420762H1
2222
2480


79
LG:230151.1:2000SEP08
6868146H1
2238
2846


79
LG:230151.1:2000SEP08
2692033H1
1
265


79
LG:230151.1:2000SEP08
3345531H1
21
275


79
LG:230151.1:2000SEP08
g1990900
206
488


79
LG:230151.1:2000SEP08
6057493H1
746
984


79
LG:230151.1:2000SEP08
6057493F6
746
984


79
LG:230151.1:2000SEP08
6057493F8
746
971


79
LG:230151.1:2000SEP08
7625371J1
821
1444


79
LG:230151.1:2000SEP08
198957R7
923
1449


79
LG:230151.1:2000SEP08
198957H1
923
1108


79
LG:230151.1:2000SEP08
g1400401
1048
1444


79
LG:230151.1:2000SEP08
4330089H1
194
378


79
LG:230151.1:2000SEP08
7276116H2
85
666


79
LG:230151.1:2000SEP08
5386485F7
114
726


79
LG:230151.1:2000SEP08
5334046F6
553
998


79
LG:230151.1:2000SEP08
g1400455
625
896


79
LG:230151.1:2000SEP08
6057485H1
746
984


79
LG:230151.1:2000SEP08
2864522H1
2856
3146


79
LG:230151.1:2000SEP08
7578937H1
74
626


79
LG:230151.1:2000SEP08
2692033F6
1
503


79
LG:230151.1:2000SEP08
g3842498
2881
2935


79
LG:230151.1:2000SEP08
2160735H1
2194
2444


79
LG:230151.1:2000SEP08
2160580H1
2194
2448


79
LG:230151.1:2000SEP08
2160735F6
2194
2588


79
LG:230151.1:2000SEP08
9846162
2111
2428


79
LG:230151.1:2000SEP08
6298190H1
2469
2740


79
LG:230151.1:2000SEP08
1208532H1
2479
2545


79
LG:230151.1:2000SEP08
1209024R6
2479
2912


79
LG:230151.1:2000SEP08
1209024H1
2479
2707


79
LG:230151.1:2000SEP08
4163123H1
2497
2793


79
LG:230151.1:2000SEP08
2834338H1
1524
1795


79
LG:230151.1:2000SEP08
4420745H1
2222
2481


79
LG:230151.1:2000SEP08
1006278H1
1879
2136


79
LG:230151.1:2000SEP08
6138222H1
2058
2353


79
LG:230151.1:2000SEP08
g694907
2556
2842


79
LG:230151.1:2000SEP08
550609R1
2596
2935


79
LG:230151.1:2000SEP08
7164680H1
1751
2245


79
LG:230151.1:2000SEP08
1209024T6
2657
2912


79
LG:230151.1:2000SEP08
19895717
2677
2912


79
LG:230151.1:2000SEP08
6763572J1
2731
2935


79
LG:230151.1:2000SEP08
g1760656
2747
2935


79
LG:230151.1:2000SEP08
g3050231
2754
2935


79
LG:230151.1:2000SEP08
7330830H2
2761
2912


79
LG:230151.1:2000SEP08
g2900238
2765
2935


79
LG:230151.1:2000SEP08
92552192
2776
2899


79
LG:230151.1:2000SEP08
3889714H1
2780
2933


79
LG:230151.1:2000SEP08
5443914H1
2800
2912


79
LG:230151.1:2000SEP08
550609R6
2596
2899


79
LG:230151.1:2000SEP08
550609H1
2596
2866


79
LG:230151.1:2000SEP08
550609F1
2605
2912


79
LG:230151.1:2000SEP08
2588088T6
2627
2912


79
LG:230151.1:2000SEP08
4552816H1
2636
2890


79
LG:230151.1:2000SEP08
7066009H1
352
929


79
LG:230151.1:2000SEP08
5334046H1
551
803


79
LG:230151.1:2000SEP08
2991485H1
31
350


79
LG:230151.1:2000SEP08
575414H1
22
274


79
LG:230151.1:2000SEP08
4330089F6
193
405


79
LG:230151.1:2000SEP08
4522461H1
2272
2525


80
LG:215158.5:2000SEP08
4763386T8
1213
1407


80
LG:215158.5:2000SEP08
7685125H1
857
1413


80
LG:215158.5:2000SEP08
2049848H1
1197
1422


80
LG:215158.5:2000SEP08
4521902H1
1212
1464


80
LG:215158.5:2000SEP08
4786255H2
1251
1440


80
LG:215158.5:2000SEP08
7685425H1
857
1429


80
LG:215158.5:2000SEP08
5268360H1
1386
1567


80
LG:215158.5:2000SEP08
g5424826
1234
1567


80
LG:215158.5:2000SEP08
g4302729
1116
1566


80
LG:215158.5:2000SEP08
g3677733
1123
1565


80
LG:215158.5:2000SEP08
g3899457
1243
1562


80
LG:215158.5:2000SEP08
g4069202
1105
1563


80
LG:215158.5:2000SEP08
g3092998
1300
1563


80
LG:215158.5:2000SEP08
7733923H2
992
1563


80
LG:215158.5:2000SEP08
g3422887
1118
1562


80
LG:215158.5:2000SEP08
g3178427
1194
1562


80
LG:215158.5:2000SEP08
g3888239
1147
1559


80
LG:215158.5:2000SEP08
g3418799
1142
1559


80
LG:215158.5:2000SEP08
g2354334
1103
1559


80
LG:215158.5:2000SEP08
g4763433
1106
1559


80
LG:215158.5:2000SEP08
1892668H1
1443
1559


80
LG:215158.5:2000SEP08
1896066H1
1443
1559


80
LG:215158.5:2000SEP08
94852805
1188
1559


80
LG:215158.5:2000SEP08
2288404R6
1151
1559


80
LG:215158.5:2000SEP08
g5811280
1154
1559


80
LG:215158.5:2000SEP08
1940511H1
1432
1559


80
LG:215158.5:2000SEP08
g4534757
1095
1559


80
LG:215158.5:2000SEP08
g2751206
1160
1559


80
LG:215158.5:2000SEP08
2569722R6
1021
1559


80
LG:215158.5:2000SEP08
g5595406
1393
1559


80
LG:215158.5:2000SEP08
3367729H1
1166
1450


80
LG:215158.5:2000SEP08
4116953H1
1126
1409


80
LG:215158.5:2000SEP08
1421186H1
761
937


80
LG:215158.5:2000SEP08
2494871H1
671
892


80
LG:215158.5:2000SEP08
7756888J1
620
798


80
LG:215158.5:2000SEP08
1795373H1
671
859


80
LG:215158.5:2000SEP08
5412690H1
648
831


80
LG:215158.5:2000SEP08
2288404H1
1151
1409


80
LG:215158.5:2000SEP08
6009736H1
1180
1452


80
LG:215158.5:2000SEP08
3818074H1
1260
1416


80
LG:215158.5:2000SEP08
3737368H1
1407
1565


80
LG:215158.5:2000SEP08
5268301H1
1386
1566


80
LG:215158.5:2000SEP08
3235146H2
717
964


80
LG:215158.5:2000SEP08
4423550H1
760
1011


80
LG:215158.5:2000SEP08
4294737H1
752
1006


80
LG:215158.5:2000SEP08
3113570H1
705
981


80
LG:215158.5:2000SEP08
4298616H1
720
982


80
LG:215158.5:2000SEP08
4320510H1
724
981


80
LG:215158.5:2000SEP08
4312194H1
703
980


80
LG:215158.5:2000SEP08
4422714H1
760
980


80
LG:215158.5:2000SEP08
4709902H1
682
975


80
LG:215158.5:2000SEP08
4522027H1
693
974


80
LG:215158.5:2000SEP08
854561H1
725
974


80
LG:215158.5:2000SEP08
5519235H1
830
966


80
LG:215158.5:2000SEP08
5510860H1
815
1045


80
LG:215158.5:2000SEP08
4225332H1
774
1047


80
LG:215158.5:2000SEP08
5988296H1
762
1040


80
LG:215158.5:2000SEP08
5653555H1
669
1043


80
LG:215158.5:2000SEP08
5987596H1
762
1026


80
LG:215158.5:2000SEP08
4251767H1
759
1020


80
LG:215158.5:2000SEP08
4133284H2
767
1008


80
LG:215158.5:2000SEP08
4435292H2
1223
1486


80
LG:215158.5:2000SEP08
5025207H1
1213
1448


80
LG:215158.5:2000SEP08
4978535H1
1223
1479


80
LG:215158.5:2000SEP08
2601426H1
1252
1477


80
LG:215158.5:2000SEP08
2639036H1
1232
1477


80
LG:215158.5:2000SEP08
4977553H1
1250
1512


80
LG:215158.5:2000SEP08
5853283H1
1255
1510


80
LG:215158.5:2000SEP08
2181480F6
1048
1502


80
LG:215158.5:2000SEP08
2181480H1
1215
1502


80
LG:215158.5:2000SEP08
3210731H1
1241
1499


80
LG:215158.5:2000SEP08
6129209H1
972
1493


80
LG:215158.5:2000SEP08
509861H1
1017
1229


80
LG:215158.5:2000SEP08
4342493H1
907
1221


80
LG:215158.5:2000SEP08
7096676H1
725
1208


80
LG:215158.5:2000SEP08
5965723H1
749
1199


80
LG:215158.5:2000SEP08
4001315H1
1041
1194


80
LG:215158.5:2000SEP08
6444667H1
714
1192


80
LG:215158.5:2000SEP08
g6659667
710
1120


80
LG:215158.5:2000SEP08
5961576H1
715
1139


80
LG:215158.5:2000SEP08
3097624H1
816
1107


80
LG:215158.5:2000SEP08
5519335H1
830
1089


80
LG:215158.5:2000SEP08
5564744T9
828
1336


80
LG:215158.5:2000SEP08
854561R1
725
1344


80
LG:215158.5:2000SEP08
1003336R1
888
1374


80
LG:215158.5:2000SEP08
1003336H1
1100
1374


80
LG:215158.5:2000SEP08
2569722H1
1021
1325


80
LG:215158.5:2000SEP08
6890146J1
909
1316


80
LG:215158.5:2000SEP08
4511922H1
1068
1310


80
LG:215158.5:2000SEP08
3272493T6
749
1244


80
LG:215158.5:2000SEP08
3729041H1
1048
1279


80
LG:215158.5:2000SEP08
5965623H1
718
1285


80
LG:215158.5:2000SEP08
4622635H1
1064
1315


80
LG:215158.5:2000SEP08
4292907H1
1038
1296


80
LG:215158.5:2000SEP08
4763386T9
850
1479


80
LG:215158.5:2000SEP08
7685225H1
864
1489


80
LG:215158.5:2000SEP08
7419422T1
844
1457


80
LG:215158.5:2000SEP08
7060657H1
920
1499


80
LG:215158.5:2000SEP08
4325938H1
1326
1508


80
LG:215158.5:2000SEP08
4322970H1
1294
1491


80
LG:215158.5:2000SEP08
4005972H1
1242
1487


80
LG:215158.5:2000SEP08
5948161H1
1242
1521


80
LG:215158.5:2000SEP08
94510841
1367
1555


80
LG:215158.5:2000SEP08
g4395334
1123
1554


80
LG:215158.5:2000SEP08
g5591405
1366
1553


80
LG:215158.5:2000SEP08
g2595148
1258
1553


80
LG:215158.5:2000SEP08
5512202H1
1303
1551


80
LG:215158.5:2000SEP08
g2198087
1121
1536


80
LG:215158.5:2000SEP08
3729041T1
1049
1522


80
LG:215158.5:2000SEP08
7930783H1
918
1556


80
LG:215158.5:2000SEP08
1831292H1
1274
1523


80
LG:215158.5:2000SEP08
5034338T6
1073
1521


80
LG:215158.5:2000SEP08
2181480T6
1200
1521


80
LG:215158.5:2000SEP08
2288404T6
1139
1521


80
LG:215158.5:2000SEP08
2569722T6
1021
1517


80
LG:215158.5:2000SEP08
6727494H1
732
1343


80
LG:215158.5:2000SEP08
1423205H1
1204
1445


80
LG:215158.5:2000SEP08
6401017H1
1160
1405


80
LG:215158.5:2000SEP08
5984486H1
1192
1483


80
LG:215158.5:2000SEP08
g4075380
979
1353


80
LG:215158.5:2000SEP08
2375777H1
1216
1437


80
LG:215158.5:2000SEP08
3762291H1
1163
1433


80
LG:215158.5:2000SEP08
g3181429
1153
1559


80
LG:215158.5:2000SEP08
1896331H1
1443
1559


80
LG:215158.5:2000SEP08
g4004067
1170
1556


80
LG:215158.5:2000SEP08
6058031H1
721
782


80
LG:215158.5:2000SEP08
3097624F6
214
720


80
LG:215158.5:2000SEP08
5294643H1
404
570


80
LG:215158.5:2000SEP08
3097624T6
1
438


81
LG:235840.1:2000SEP08
2676570F6
2277
2647


81
LG:235840.1:2000SEP08
2676570T6
2277
2655


81
LG:235840.1:2000SEP08
g3744074
2254
2704


81
LG:235840.1:2000SEP08
3992215H1
1800
2095


81
LG:235840.1:2000SEP08
7193758H2
1810
2237


81
LG:235840.1:2000SEP08
g2836920
2235
2701


81
LG:235840.1:2000SEP08
5835079H1
2239
2462


81
LG:235840.1:2000SEP08
g2238015
2338
2683


81
LG:235840.1:2000SEP08
g2737235
2301
2666


81
LG:235840.1:2000SEP08
g2669827
2286
2666


81
LG:235840.1:2000SEP08
g692242
2389
2711


81
LG:235840.1:2000SEP08
g2575700
2357
2637


81
LG:235840.1:2000SEP08
1451436T6
2352
2667


81
LG:235840.1:2000SEP08
2549073H1
2351
2602


81
LG:235840.1:2000SEP08
4249979F6
1
363


81
LG:235840.1:2000SEP08
942891R1
2442
2707


81
LG:235840.1:2000SEP08
5187170H1
2459
2666


81
LG:235840.1:2000SEP08
g2727328
2478
2695


81
LG:235840.1:2000SEP08
g6197748
2554
2664


81
LG:235840.1:2000SEP08
g1391398
2413
2703


81
LG:235840.1:2000SEP08
729197H1
2442
2666


81
LG:235840.1:2000SEP08
942891R6
2442
2707


81
LG:235840.1:2000SEP08
g2705998
2407
2701


81
LG:235840.1:2000SEP08
g1967662
1129
1516


81
LG:235840.1:2000SEP08
5286802H1
1076
1250


81
LG:235840.1:2000SEP08
3595241H1
941
1230


81
LG:235840.1:2000SEP08
5914590H1
976
1212


81
LG:235840.1:2000SEP08
5914590F8
976
1536


81
LG:235840.1:2000SEP08
7633624H1
586
1140


81
LG:235840.1:2000SEP08
4725620H1
503
767


81
LG:235840.1:2000SEP08
g928335
600
888


81
LG:235840.1:2000SEP08
4249979H1
1
247


81
LG:235840.1:2000SEP08
7659126H1
21
526


81
LG:235840.1:2000SEP08
4249979R6
89
580


81
LG:235840.1:2000SEP08
7633624J1
394
1002


81
LG:235840.1:2000SEP08
5411412H1
1297
1562


81
LG:235840.1:2000SEP08
5501637F6
1303
1503


81
LG:235840.1:2000SEP08
5501637H1
1303
1538


81
LG:235840.1:2000SEP08
g1932950
1379
1864


81
LG:235840.1:2000SEP08
7613750J1
1195
1784


81
LG:235840.1:2000SEP08
4243528H1
1218
1465


81
LG:235840.1:2000SEP08
4664169H1
1222
1414


81
LG:235840.1:2000SEP08
4664169F6
1222
1675


81
LG:235840.1:2000SEP08
5511564H1
1222
1385


81
LG:235840.1:2000SEP08
6306648H1
1230
1694


81
LG:235840.1:2000SEP08
1451436F1
1500
1933


81
LG:235840.1:2000SEP08
1451436F6
1500
2008


81
LG:235840.1:2000SEP08
1451436H1
1500
1767


81
LG:235840.1:2000SEP08
6160452H1
1530
1821


81
LG:235840.1:2000SEP08
g1389188
1448
1703


81
LG:235840.1:2000SEP08
531327H1
1449
1692


81
LG:235840.1:2000SEP08
6334626H1
1455
1902


81
LG:2358A0.1:2000SEP08
5204143H1
1445
1709


81
LG:235840.1:2000SEP08
2286077H1
1694
1932


81
LG:235840.1:2000SEP08
5989717H1
1735
1985


81
LG:235840.1:2000SEP08
7065831H1
1614
2104


81
LG:235840.1:2000SEP08
7613750H1
1669
2267


81
LG:235840.1:2000SEP08
4898449H1
1682
1867


81
LG:235840.1:2000SEP08
3464906H1
1690
2022


81
LG:235840.1:2000SEP08
004533H1
1582
1874


81
LG:235840.1:2000SEP08
6730659H1
1604
1825


81
LG:235840.1:2000SEP08
4196254H1
2224
2519


81
LG:235840.1:2000SEP08
5914590R8
1568
2109


81
LG:235840.1:2000SEP08
2960481H2
1566
1853


81
LG:235840.1:2000SEP08
5056390H1
1578
1850


81
LG:235840.1:2000SEP08
5034382T6
2283
2679


81
LG:235840.1:2000SEP08
2676562H1
2277
2526


81
LG:235840.1:2000SEP08
5693701H1
2282
2543


81
LG:235840.1:2000SEP08
7738333H1
2045
2594


81
LG:235840.1:2000SEP08
4664169T6
2049
2595


81
LG:235840.1:2000SEP08
639274H1
2058
2332


81
LG:235840.1:2000SEP08
544137H1
2149
2293


81
LG:235840.1:2000SEP08
91270286
2033
2216


81
LG:235840.1:2000SEP08
1285809H1
1979
2216


81
LG:235840.1:2000SEP08
6442655H1
1795
2303


81
LG:235840.1:2000SEP08
6711829H1
1755
2246


81
LG:235840.1:2000SEP08
4351829H1
1735
2063


81
LG:235840.1:2000SEP08
7213696H1
1946
2423


81
LG:235840.1:2000SEP08
g692276
1883
2221


81
LG:235840.1:2000SEP08
g692306
1883
1965


81
LG:235840.1:2000SEP08
6377861H1
1919
2189


82
LG:350272.1:2000SEP08
960820R6
1570
1941


82
LG:350272.1:2000SEP08
2697244H1
1573
1858


82
LG:350272.1:2000SEP08
960820H1
1570
1845


82
LG:350272.1:2000SEP08
7326176H1
1452
1912


82
LG:350272.1:2000SEP08
6311958H1
1468
1895


82
LG:350272.1:2000SEP08
6201854H1
1480
1915


82
LG:350272.1:2000SEP08
3559406H1
1479
1582


82
LG:350272.1:2000SEP08
3490063H1
1481
1775


82
LG:350272.1:20003EP08
5020696T1
1335
1784


82
LG:350272.1:2000SEP08
2538770H1
1336
1545


82
LG:350272.1:2000SEP08
g2674996
1426
1831


82
LG:350272.1:2000SEP08
g1186534
1432
1832


82
LG:350272.1:2000SEP08
603382H1
1336
1584


82
LG:350272.1:2000SEP08
3740987H1
1339
1633


82
LG:350272.1:2000SEP08
5020588T1
1354
1783


82
LG:350272.1:2000SEP08
4241989H1
1420
1748


82
LG:350272.1:2000SEP08
581813R6
1212
1561


82
LG:350272.1:2000SEP08
7322258H1
1251
1868


82
LG:350272.1:2000SEP08
2127622H1
1277
1536


82
LG:350272.1:2000SEP08
7082642H1
857
1251


82
LG:350272.1:20003EP08
g1152456
872
1192


82
LG:350272.1:2000SEP08
g3958809
873
1219


82
LG:350272.1:2000SEP08
g3277672
873
1323


82
LG:350272.1:2000SEP08
g3249855
873
1308


82
LG:350272.1:2000SEP08
g1101302
901
1173


82
LG:350272.1:2000SEP08
g2820552
903
1337


82
LG:350272.1:2000SEP08
5020696H1
907
1173


82
LG:350272.1:2000SEP08
5062519H1
941
1210


82
LG:350272.1:2000SEP08
g3163179
974
1240


82
LG:350272.1:2000SEP08
5696180H1
1003
1267


82
LG:350272.1:2000SEP08
6821260J1
1043
1481


82
LG:350272.1:2000SEP08
3224632H2
1053
1337


82
LG:350272.1:2000SEP08
7764948H1
1150
1503


82
LG:350272.1:2000SEP08
3721403H1
1177
1425


82
LG:350272.1:2000SEP08
5865088H1
1201
1485


82
LG:350272.1:2000SEP08
581813H1
1212
1475


82
LG:350272.1:2000SEP08
4010319H1
2042
2252


82
LG:350272.1:2000SEP08
1741002T6
2042
2491


82
LG:350272.1:2000SEP08
2650967H1
2043
2222


82
LG:350272.1:2000SEP08
401 3519H1
2051
2256


82
LG:350272.1:2000SEP08
4353493H1
2051
2142


82
LG:350272.1:2000SEP08
211293H1
2348
2536


82
LG:350272.1:2000SEP08
4353485H1
2051
2140


82
LG:350272.1:2000SEP08
211114H1
2052
2102


82
LG:350272.1:2000SEP08
3621890H1
2051
2133


82
LG:350272.1:2000SEP08
581813T6
2053
2491


82
LG:350272.1:2000SEP08
211696H1
2348
2529


82
LG:350272.1:2000SEP08
g2820887
2054
2532


82
LG:350272.1:2000SEP08
1684883T6
2062
2494


82
LG:350272.1:2000SEP08
633648H1
2354
2542


82
LG:350272.1:2000SEP08
1684883F6
2062
2529


82
LG:350272.1:2000SEP08
6606673H1
2077
2530


82
LG:350272.1:2000SEP08
3565543H1
2365
2487


82
LG:350272.1:2000SEP08
g2359505
2443
2529


82
LG:350272.1:2000SEP08
g4649884
2445
2523


82
LG:350272.1:2000SEP08
g4970896
2078
2534


82
LG:350272.1:2000SEP08
g4125734
2080
2518


82
LG:350272.1:2000SEP08
g3741618
2095
2538


82
LG:350272.1:2000SEP08
g6038705
2111
2529


82
LG:350272.1:2000SEP08
g4074869
2114
2535


82
LG:350272.1:2000SEP08
g5755616
2127
2535


82
LG:350272.1:2000SEP08
g2465965
2144
2535


82
LG:350272.1:2000SEP08
92669493
2154
2531


82
LG:350272.1:2000SEP08
g461 8967
2155
2529


82
LG:350272.1:2000SEP08
g2270187
2176
2532


82
LG:350272.1:2000SEP08
9855861
2193
2526


82
LG:350272.1:2000SEP08
g5397025
2183
2529


82
LG:350272.1:2000SEP08
g3307326
2185
2538


82
LG:350272.1:2000SEP08
6615126H1
2467
2529


82
LG:350272.1:2000SEP08
g2715505
2186
2535


82
LG:350272.1:2000SEP08
g4267877
2203
2523


82
LG:350272.1:2000SEP08
g4267523
2203
2523


82
LG:350272.1:2000SEP08
g4267458
2203
2523


82
LG:350272.1:2000SEP08
1637245H1
2205
2400


82
LG:350272.1:2000SEP08
92669985
2196
2427


82
LG:350272.1:2000SEP08
2561156H1
2221
2501


82
LG:350272.1:2000SEP08
g5364704
2224
2530


82
LG:350272.1:2000SEP08
6843381H1
2239
2529


82
LG:350272.1:2000SEP08
g5755074
2262
2535


82
LG:350272.1:2000SEP08
6326064H1
2271
2532


82
LG:350272.1:2000SEP08
5306551H1
2276
2400


82
LG:350272.1:2000SEP08
644238T6
2276
2495


82
LG:350272.1:2000SEP08
5306583H1
2277
2429


82
LG:350272.1:2000SEP08
6383176H1
2285
2491


82
LG:350272.1:2000SEP08
g4079566
2287
2529


82
LG:350272.1:2000SEP08
g2577306
2288
2529


82
LG:350272.1:2000SEP08
g5812197
2319
2515


82
LG:350272.1:2000SEP08
1684883H1
2327
2529


82
LG:350272.1:2000SEP08
3932451H1
2346
2529


82
LG:350272.1:2000SEP08
6058322H1
1563
1897


82
LG:350272.1:2000SEP08
4121623H1
1566
1861


82
LG:350272.1:2000SEP08
1888879H1
1519
1804


82
LG:350272.1:2000SEP08
4665428H1
1578
1849


82
LG:350272.1:2000SEP08
708387H1
1595
1868


82
LG:350272.1:2000SEP08
g3213833
1605
1830


82
LG:350272.1:2000SEP08
2715220H1
1611
1854


82
LG:350272.1:2000SEP08
g2575091
1627
1878


82
LG:350272.1:2000SEP08
6486886H1
1625
2162


82
LG:350272.1:2000SEP08
2206242H1
1627
1874


82
LG:350272.1:2000SEP08
6821260H1
710
1191


82
LG:350272.1:2000SEP08
7746167H1
848
1336


82
LG:350272.1:2000SEP08
3107667H1
1
210


82
LG:350272.1:2000SEP08
7674927H2
133
323


82
LG:350272.1:2000SEP08
754982H 1
168
390


82
LG:350272.1:2000SEP08
7346935H1
183
661


82
LG:350272.1:2000SEP08
g4685374
380
855


82
LG:350272.1:2000SEP08
g5878247
383
855


82
LG:350272.1:2000SEP08
7313314H1
494
846


82
LG:350272.1:2000SEP08
g4649651
510
855


82
LG:350272.1:2000SEP08
g3191587
668
829


82
LG:350272.1:2000SEP08
g4889943
847
1276


82
LG:350272.1:2000SEP08
3844367H1
1634
1945


82
LG:350272.1:2000SEP08
g2900340
1644
1819


82
LG:350272.1:2000SEP08
2805489H1
1667
1917


82
LG:350272.1:2000SEP08
5766360H1
1673
2184


82
LG:350272.1:2000SEP08
3016843H1
1699
1895


82
LG:350272.1:2000SEP08
6552652H1
1766
2282


82
LG:350272.1:2000SEP08
6552052H1
1766
2225


82
LG:350272.1:2000SEP08
4138187H1
1789
1895


82
LG:350272.1:2000SEP08
1864387H1
1808
1895


82
LG:350272.1:2000SEP08
2116744H1
1814
1895


82
LG:350272.1:2000SEP08
g855860
1834
2117


82
LG:350272.1:2000SEP08
644363H1
1838
2105


82
LG:350272.1:2000SEP08
644238R6
1838
2391


82
LG:350272.1:2000SEP08
960820T6
2038
2494


82
LG:350272.1:2000SEP08
1741002R6
2042
2529


82
LG:350272.1:2000SEP08
644238H1
1838
1895


82
LG:350272.1:2000SEP08
4003545H1
1838
2130


82
LG:350272.1:2000SEP08
2511182H1
2025
2335


82
LG:350272.1:2000SEP08
4010536H1
2032
2258


82
LG:350272.1:2000SEP08
1741002H1
2042
2126


83
LG:232190.1:2000SEP08
g2167858
814
1312


83
LG:232190.1:2000SEP08
g1156558
703
1032


83
LG:232190.1:2000SEP08
5306856H1
1123
1290


83
LG:232190.1:2000SEP08
g5634396
1222
1537


83
LG:232190.1:2000SEP08
g2167859
1241
1547


83
LG:232190.1:2000SEP08
g994115
1241
1454


83
LG:232190.1:2000SEP08
3258260H1
1243
1531


83
LG:232190.1:2000SEP08
3377873H1
1448
1636


83
LG:232190.1:2000SEP08
g4703402
1088
1535


83
LG:232190.1:2000SEP08
5968471H1
846
1393


83
LG:232190.1:2000SEP08
g3918602
281
656


83
LG:232190.1:2000SEP08
g1138172
279
576


83
LG:232190.1:2000SEP08
7069816H1
1
140


83
LG:232190.1:2000SEP08
7459387H1
1
526


83
LG:232190.1:2000SEP08
7594566H1
36
614


83
LG:232190.1:2000SEP08
2531179F7
375
578


83
LG:232190.1:2000SEP08
2531179H1
375
622


83
LG:232190.1:2000SEP08
6344340H1
377
647


83
LG:232190.1:2000SEP08
2729623F6
639
1097


83
LG:232190.1:2000SEP08
2729623H1
639
894


83
LG:232190.1:2000SEP08
7111074H1
500
934


83
LG:232190.1:2000SEP08
5306756H1
1123
1282


84
LG:1068127.1:2000SEP08
4914013T8
203
711


84
LG:1068127.1:2000SEP08
5316376T8
229
557


84
LG:1068127.1:2000SEP08
6267691F8
1
546


84
LG:1068127.1:2000SEP08
6267691H1
1
492


84
LG:1068127.1:2000SEP08
5491715F6
11
484


84
LG:1068127.1:2000SEP08
7102152H1
334
484


84
LG:1068127.1:2000SEP08
7102152F8
334
484


84
LG:1068127.1:2000SEP08
7102152R8
334
492


84
LG:1068127.1:2000SEP08
5316376F8
230
655


84
LG:1068127.1:2000SEP08
5316376H1
230
385


85
LG:408751.3:2000SEP08
5379139H1
434
679


85
LG:408751.3:2000SEP08
7587582H1
484
1051


85
LG:408751.3:2000SEP08
6868778H1
494
1117


85
LG:408751.3:2000SEP08
7067123H1
525
1070


85
LG:408751.3:2000SEP08
1270695H1
572
804


85
LG:408751.3:2000SEP08
533539H1
427
622


85
LG:408751.3:2000SEP08
1270695F6
544
830


85
LG:408751.3:2000SEP08
2707020H1
588
881


85
LG:408751.3:2000SEP08
4092963H1
327
609


85
LG:408751.3:2000SEP08
g677813
336
565


85
LG:408751.3:2000SEP08
g614162
336
605


85
LG:408751.3:2000SEP08
6985794H1
338
794


85
LG:408751.3:2000SEP08
7359626H1
379
948


85
LG:408751.3:2000SEP08
4338771H1
359
628


85
LG:408751.3:2000SEP08
g708822
393
694


85
LG:408751.3:2000SEP08
g764692
395
736


85
LG:408751.3:2000SEP08
g816062
372
784


85
LG:408751.3:2000SEP08
7587293H1
379
952


85
LG:408751.3:2000SEP08
3864471H1
374
591


85
LG:408751.3:2000SEP08
6990907H1
383
885


85
LG:408751.3:2000SEP08
6866026H1
381
974


85
LG:408751.3:2000SEP08
5674272H1
391
645


85
LG:408751.3:2000SEP08
6120160H1
391
790


85
LG:408751.3:2000SEP08
6448066H1
412
963


85
LG:408751.3:2000SEP08
7580272H1
393
907


85
LG:408751.3:2000SEP08
g691925
443
755


85
LG:408751.3:2000SEP08
533539R6
424
939


85
LG:408751.3:2000SEP08
4705993H1
1999
2149


85
LG:408751.3:2000SEP08
7158434H1
2001
2270


85
LG:408751.3:2000SEP08
6983326H1
2077
2666


85
LG:408751.3:2000SEP08
6770575H1
2300
2823


85
LG:408751.3:2000SEP08
6765966H1
2133
2654


85
LG:408751.3:2000SEP08
7580816H1
2166
2665


85
LG:408751.3:2000SEP08
1270536H1
2175
2415


85
LG:408751.3:2000SEP08
7281449H1
2232
2815


85
LG:408751.3:2000SEP08
7582690H1
2242
2758


85
LG:408751.3:2000SEP08
7275431J1
2370
2836


85
LG:408751.3:2000SEP08
5920291H1
208
267


85
LG:408751.3:2000SEP08
1456735F6
189
605


85
LG:408751.3:2000SEP08
6721132H1
193
579


85
LG:408751.3:2000SEP08
4203426H1
212
337


85
LG:408751.3:2000SEP08
1992224H1
206
475


85
LG:408751.3:2000SEP08
7259028H1
204
579


85
LG:408751.3:2000SEP08
g766593
289
587


85
LG:408751.3:2000SEP08
7058996H1
309
890


85
LG:408751.3:2000SEP08
g570855
2997
3307


85
LG:408751.3:2000SEP08
5371992H1
3015
3187


85
LG:408751.3:2000SEP08
g389944
3100
3330


85
LG:408751.3:2000SEP08
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3191
3330


85
LG:408751.3:2000SEP08
2416693H1
3191
3330


85
LG:408751.3:2000SEP08
g318775
3202
3330


85
LG:408751.3:2000SEP08
1594111H1
3236
3330


85
LG:408751.3:2000SEP08
g389942
3242
3330


85
LG:408751.3:2000SEP08
5406949T6
1495
1919


85
LG:408751.3:2000SEP08
5945223H1
1574
1656


85
LG:408751.3:2000SEP08
6773005H1
1585
2157


85
LG:408751.3:2000SEP08
6869723H1
1599
1944


85
LG:408751.3:2000SEP08
g2985356
1730
1957


85
LG:408751.3:2000SEP08
6768978H1
1703
2265


85
LG:408751.3:2000SEP08
2154505H1
1905
2188


85
LG:408751.3:2000SEP08
7585176H1
1906
2405


85
LG:408751.3:2000SEP08
2154505F7
1906
2204


85
LG:408751.3:2000SEP08
6871487H1
1928
2449


85
LG:408751.3:2000SEP08
g2003420
1937
2178


85
LG:408751.3:2000SEP08
g5553670
1949
2370


85
LG:408751.3:2000SEP08
1456735H1
208
332


85
LG:408751.3:2000SEP08
g677040
204
322


85
LG:408751.3:2000SEP08
g1950097
237
294


85
LG:408751.3:2000SEP08
7290347H1
188
672


85
LG:408751.3:2000SEP08
7290834H1
187
505


85
LG:408751.3:2000SEP08
g4152281
207
277


85
LG:408751.3:2000SEP08
g1627181
208
330


85
LG:408751.3:2000SEP08
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181
421


85
LG:408751.3:2000SEP08
3944530H1
184
461


85
LG:408751.3:2000SEP08
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181
469


85
LG:408751.3:2000SEP08
7411039H1
2627
3182


85
LG:408751.3:2000SEP08
1270292F6
2718
2996


85
LG:408751.3:2000SEP08
1270292H1
2718
2955


85
LG:408751.3:2000SEP08
6984280R8
2735
3167


85
LG:408751.3:2000SEP08
6984280H1
2735
3103


85
LG:408751.3:2000SEP08
6984280F8
2736
3174


85
LG:408751.3:2000SEP08
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2882
3147


85
LG:408751.3:2000SEP08
6985157H1
2882
3147


85
LG:408751.3:2000SEP08
g1991410
2636
2766


85
LG:408751.3:2000SEP08
g1044150
2643
2837


85
LG:408751.3:2000SEP08
6985157F8
2882
3146


85
LG:408751.3:2000SEP08
g616005
2959
3306


85
LG:408751.3:2000SEP08
4203459F6
2962
3331


85
LG:408751.3:2000SEP08
6508635H1
2987
3173


85
LG:408751.3:2000SEP08
7360836H1
2990
3331


85
LG:408751.3:2000SEP08
6447490H1
2382
2954


85
LG:408751.3:2000SEP08
7581728H1
2401
2932


85
LG:408751.3:2000SEP08
5922289H1
2401
2668


85
LG:408751.3:2000SEP08
7188176H1
2446
3010


85
LG:408751.3:2000SEP08
574501H1
2482
2729


85
LG:408751.3:2000SEP08
3460095H1
2587
2837


85
LG:408751.3:2000SEP08
7583983H1
2588
3127


85
LG:408751.3:2000SEP08
1270279H1
2603
2823


85
LG:408751.3:2000SEP08
g615297
1339
1671


85
LG:408751.3:2000SEP08
g517687
1339
1669


85
LG:408751.3:2000SEP08
g615578
1385
1671


85
LG:408751.3:2000SEP08
g614283
1381
1664


85
LG:408751.3:2000SEP08
7361584H1
1393
1931


85
LG:408751.3:2000SEP08
1456735T6
1430
1632


85
LG:408751.3:2000SEP08
g4328099
1512
1729


85
LG:408751.3:2000SEP08
g614262
1457
1664


85
LG:408751.3:2000SEP08
g4152278
1463
1663


85
LG:408751.3:2000SEP08
g562532
1469
1664


85
LG:408751.3:2000SEP08
g671207
1470
1664


85
LG:408751.3:2000SEP08
5407853T6
1462
1920


85
LG:408751.3:2000SEP08
g4148449
1491
1946


85
LG:408751.3:2000SEP08
7275431H2
1463
2036


85
LG:408751.3:2000SEP08
6572506H1
1480
2041


85
LG:408751.3:2000SEP08
7410777H1
1480
2021


85
LG:408751.3:2000SEP08
g5511164
1289
1671


85
LG:408751.3:2000SEP08
g3649444
1290
1673


85
LG:408751.3:2000SEP08
g314750
1302
1671


85
LG:408751.3:2000SEP08
g775420
1276
1685


85
LG:408751.3:2000SEP08
g4617815
1287
1678


85
LG:408751.3:2000SEP08
g314920
1339
1671


85
LG:408751.3:2000SEP08
1270695T6
1192
1632


85
LG:408751.3:2000SEP08
4717574T6
1201
1650


85
LG:408751.3:2000SEP08
1476570F6
1203
1671


85
LG:408751.3:2000SEP08
1476571F6
1203
1547


85
LG:408751.3:2000SEP08
1476570H1
1203
1409


85
LG:408751.3:2000SEP08
g614326
1215
1678


85
LG:408751.3:2000SEP08
1476571T6
1221
1634


85
LG:408751.3:2000SEP08
g4152280
1234
1403


85
LG:408751.3:2000SEP08
g4598685
1244
1672


85
LG:408751.3:2000SEP08
2153570H1
1256
1530


85
LG:408751.3:2000SEP08
g314775
1258
1671


85
LG:408751.3:2000SEP08
4492503H1
1264
1672


85
LG:408751.3:2000SEP08
g61 5988
1270
1671


85
LG:408751.3:2000SEP08
g4223790
827
1266


85
LG:408751.3:2000SEP08
5407853F6
814
1181


85
LG:408751.3:2000SEP08
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833
1295


85
LG:408751.3:2000SEP08
7160561H1
835
1188


85
LG:408751.3:2000SEP08
g3331126
848
1268


85
LG:408751.3:2000SEP08
5310872H1
850
1076


85
LG:408751.3:2000SEP08
73881 16H1
852
1314


85
LG:408751.3:2000SEP08
g6992853
862
1266


85
LG:408751.3:2000SEP08
5267191H1
869
1129


85
LG:408751.3:20003EP08
4940779H1
890
1162


85
LG:408751.3:2000SEP08
1270258H1
892
1130


85
LG:408751.3:2000SEP08
g794503
898
1291


85
LG:408751.3:2000SEP08
g816007
896
1257


85
LG:408751.3:2000SEP08
g901436
904
1267


85
LG:408751.3:2000SEP08
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597
836


85
LG:408751.3:2000SEP08
5498383F6
573
1056


85
LG:408751.3:2000SEP08
5498383H1
573
811


85
LG:408751.3:2000SEP08
5311056H1
591
753


85
LG:408751.3:2000SEP08
7372949H1
644
1194


85
LG:408751.3:2000SEP08
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671
950


85
LG:408751.3:2000SEP08
5924427H1
693
983


85
LG:408751.3:2000SEP08
6869327H1
736
1241


85
LG:408751.3:2000SEP08
5406949H1
814
1046


85
LG:408751.3:2000SEP08
6984258H1
733
1127


85
LG:408751.3:2000SEP08
5406949F6
814
981


85
LG408751.3:2000SEP08
009349H1
773
1119


85
LG:408751.3:2000SEP08
6888770H1
784
1299


85
LG:408751.3:2000SEP08
4943311T6
797
1243


85
LG:408751.3:2000SEP08
7279978H1
787
1322


85
LG:408751.3:2000SEP08
7292792H1
805
1378


85
LG:408751.3:2000SEP08
g1192539
814
1266


85
LG:408751.3:2000SEP08
6037020H1
802
1344


85
LG:408751.3:2000SEP08
5407853H1
814
940


85
LG:408751.3:2000SEP08
4705993T9
1119
1569


85
LG:408751.3:2000SEP08
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1179
1438


85
LG:408751.3:2000SEP08
1476570T6
1187
1631


85
LG:408751.3:2000SEP08
748579H1
1095
1335


85
LG:408751.3:2000SEP08
748579R1
1091
1668


85
LG:408751.3:2000SEP08
859218T6
1028
1600


85
LG:408751.3:2000SEP08
6855475H1
1028
1225


85
LG:408751.3:2000SEP08
6871051H1
1080
1596


85
LG:408751.3:2000SEP08
1270292T6
1031
1592


85
LG:408751.3:2000SEP08
g822109
1041
1250


85
LG:408751.3:2000SEP08
2416693T6
1106
1626


85
LG:408751.3:2000SEP08
g6086997
914
1274


85
LG:408751.3:2000SEP08
533539T6
921
1238


85
LG:408751.3:2000SEP08
5371992T9
928
1565


85
LG:408751.3:2000SEP08
g314842
931
1237


85
LG:408751.3:2000SEP08
g683067
953
1236


85
LG:408751.3:2000SEP08
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961
1496


85
LG:408751.3:2000SEP08
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990
1510


85
LG:408751.3:2000SEP08
859218H1
990
1204


85
LG:408751.3:2000SEP08
859218R6
990
1432


85
LG:408751.3:2000SEP08
g567610
995
1237


85
LG:408751.3:2000SEP08
4943311H1
175
458


85
LG:408751.3:2000SEP08
4943311F6
175
595


85
LG:408751.3:2000SEP08
6818987H1
197
267


85
LG:408751.3:2000SEP08
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181
790


85
LG:408751.3:2000SEP08
g1978747
1
307


85
LG:408751.3:2000SEP08
g5553287
1
315


85
LG:408751.3:2000SEP08
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33
250


85
LG:408751.3:2000SEP08
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1
436


85
LG:408751.3:2000SEP08
6955370H1
22
540


85
LG:408751.3:2000SEP08
g6701393
25
503


85
LG:408751.3:2000SEP08
g4390046
24
500


85
LG:408751.3:2000SEP08
g4534562
24
504


85
LG:408751.3:2000SEP08
g1192915
25
170


85
LG:408751.3:2000SEP08
g2003054
31
344


85
LG:408751.3:2000SEP08
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35
555


85
LG:408751.3:2000SEP08
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33
460


85
LG:408751.3:2000SEP08
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33
631


85
LG:408751.3:2000SEP08
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33
606


85
LG:408751.3:2000SEP08
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33
637


85
LG:408751.3:2000SEP08
6818431J1
33
570


85
LG:408751.3:2000SEP08
g2003419
45
421


85
LG:408751.3:2000SEP08
g1551472
61
213


85
LG:408751.3:2000SEP08
6147606H1
71
625


85
LG:408751.3:2000SEP08
g615579
115
462


85
LG:408751.3:2000SEP08
g389770
122
510


85
LG:408751.3:2000SEP08
5311056F8
141
753


85
LG:408751.3:2000SEP08
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153
753


85
LG:408751.3:2000SEP08
g615989
174
503


86
LG:1078933.1:2000SEP08
2730285H1
654
890


86
LG:1078933.1:2000SEP08
g2728816
753
922


86
LG:1078933.1:2000SEP08
4002923H1
773
1072


86
LG:1078933.1:2000SEP08
g2537503
800
1089


86
LG:1078933.1:2000SEP08
g6299364
1051
1124


86
LG:1078933.1:2000SEP08
4992604T6
442
970


86
LG:1078933.1:2000SEP08
2795327H1
459
701


86
LG:1078933.1:2000SEP08
6000894T8
511
998


86
LG:1078933.1:2000SEP08
4992604F6
1 561


86
LG:1078933.1:2000SEP08
4992604H1
1
207


86
LG:1078933.1:2000SEP08
7264011H1
45
555


86
LG:1078933.1:2000SEP08
4251691H1
398
656


86
LG:1078933.1:2000SEP08
5305837H1
410
651


86
LG:1078933.1:2000SEP08
2651913F6
438
990


86
LG:1078933.1:2000SEP08
2651913H1
438
683


86
LG:1078933.1:2000SEP08
1720617T6
592
1054


86
LG:1078933.1:2000SEP08
4030861T6
612
1166


87
LG:958731.1:2000SEP08
6274461H2
1
390


87
LG:958731.1:2000SEP08
6274461F8
1
586


87
LG:958731.1:2000SEP08
6274461T8
394
1095


88
LG:024125.5:2000SEP08
7937162H1
1
577


88
LG:024125.5:2000SEP08
3359165H1
14
254


88
LG:024125.5:2000SEP08
927867H1
28
176


88
LG:024125.5:2000SEP08
4729644H1
32
297


88
LG:024125.5:2000SEP08
g5430947
34
309


88
LG:024125.5:2000SEP08
g6300785
626
783


88
LG:024125.5:2000SEP08
g3918107
627
783


88
LG:024125.5:2000SEP08
1848687T6
640
818


88
LG:024125.5:2000SEP08
g4078394
641
783


88
LG:024125.5:2000SEP08
g6301603
646
783


88
LG:024125.5:2000SEP08
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671
783


88
LG:024125.5:2000SEP08
3799006H1
673
805


88
LG:024125.5:2000SEP08
g5531063
676
783


88
LG:024125.5:2000SEP08
g2115664
677
783


88
LG:024125.5:2000SEP08
g4004611
682
783


88
LG:024125.5:2000SEP08
g3417887
690
783


88
LG:024125.5:2000SEP08
g3422421
690
783


88
LG:024125.5:2000SEP08
g1141030
716
783


88
LG:024125.5:2000SEP08
g3078258
744
820


88
LG:024125.5:2000SEP08
g873980
752
809


88
LG:024125.5:2000SEP08
g5431328
622
805


88
LG:024125.5:2000SEP08
1528650H1
625
829


88
LG:024125.5:2000SEP08
3246738H1
568
823


88
LG:024125.5:2000SEP08
4544253H1
571
808


88
LG:024125.5:2000SEP08
4329943H1
557
759


88
LG:024125.5:2000SEP08
4270595H1
567
820


88
LG:024125.5:2000SEP08
2995696H1
549
800


88
LG:024125.5:2000SEP08
4330031H1
557
745


88
LG:024125.5:2000SEP08
g6713522
513
783


88
LG:024125.5:2000SEP08
6141768H1
523
794


88
LG:024125.5:2000SEP08
2994610H1
549
783


88
LG:024125.5:2000SEP08
4625455H1
501
739


88
LG:024125.5:2000SEP08
g6300249
39
447


88
LG:024125.5:2000SEP08
1391910H1
39
303


88
LG:024125.5:2000SEP08
1439283F6
39
660


88
LG:024125.5:2000SEP08
927867R1
35
490


88
LG:024125.5:2000SEP08
3366477H1
35
308


88
LG:024125.5:2000SEP08
986481H1
47
334


88
LG:024125.5:2000SEP08
3537126H1
45
215


88
LG:024125.5:2000SEP08
986481R1
47
350


88
LG:024125.5:2000SEP08
2729856H1
48
294


88
LG:024125.5:2000SEP08
630784H1
48
135


88
LG:024125.5:2000SEP08
1235980H1
47
273


88
LG:024125.5:2000SEP08
4666859H1
48
292


88
LG:024125.5:2000SEP08
1414985H1
45
280


88
LG:024125.5:2000SEP08
1414984H1
45
284


88
LG:024125.5:2000SEP08
2279387H1
48
332


88
LG:024125.5:2000SEP08
1235980F1
47
597


88
LG:024125.5:2000SEP08
1334045H1
42
186


88
LG:024125.5:2000SEP08
3387780H1
44
342


88
LG:024125.5:2000SEP08
g677179
42
278


88
LG:024125.5:2000SEP08
g874037
43
380


88
LG:024125.5:2000SEP08
4887675H1
45
173


88
LG:024125.5:2000SEP08
3401859H1
39
267


88
LG:024125.5:2000SEP08
4747105H1
42
322


88
LG:024125.5:2000SEP08
2701713H1
40
310


88
LG:024125.5:2000SEP08
2519203H1
40
275


88
LG:024125.5:2000SEP08
4017658H1
41
293


88
LG:024125.5:2000SEP08
4843176H1
42
316


88
LG:024125.5:2000SEP08
g6300000
39
470


88
LG:024125.5:2000SEP08
896173H1
245
483


88
LG:024125.5:2000SEP08
4333283H1
264
537


88
LG:024125.5:2000SEP08
7416919T1
319
827


88
LG:024125.5:2000SEP08
5299466H1
449
716


88
LG:024125.5:2000SEP08
896173R1
245
815


88
LG:024125.5:2000SEP08
2134896H1
201
460


88
LG:024125.5:2000SEP08
7437029H1
144
631


88
LG:024125.5:2000SEP08
1399836H1
160
400


88
LG:024125.5:2000SEP08
g2011988
109
268


88
LG:024125.5:2000SEP08
6497615H1
130
683


88
LG:024125.5:2000SEP08
g2111895
48
449


88
LG:024125.5:2000SEP08
2453432H1
82
347


88
LG:024125.5:2000SEP08
3699972H1
48
336


88
LG:024125.5:2000SEP08
g1810337
51
427


88
LG:024125.5:2000SEP08
g1544548
49
170


88
LG:024125.5:2000SEP08
g1163380
48
406


89
LG:373637.3:2000SEP08
g3040122
647
903


89
LG:373637.3:2000SEP08
g2942533
587
903


89
LG:373637.3:2000SEP08
g6041238
605
900


89
LG:373637.3:2000SEP08
g3051904
649
900


89
LG:373637.3:2000SEP08
g3804542
400
782


89
LG:373637.3:2000SEP08
6245663F8
1
684


89
LG:373637.3:2000SEP08
6245663H1
1
508


89
LG:373637.3:2000SEP08
g3180013
567
1011


89
LG:373637.3:2000SEP08
g3594985
588
1008


89
LG:373637.3:2000SEP08
g5675509
577
1004


89
LG:373637.3:2000SEP08
6245663T8
237
904


89
LG:373637.3:2000SEP08
g2953832
641
903


89
LG:373637.3:2000SEP08
g6036927
493
903


89
LG:373637.3:2000SEP08
g5394478
447
903


90
LG:1053229.1:2000SEP08
1445465F6
56
334


90
LG:1053229.1:2000SEP08
6103338F7
66
595


90
LG:1053229.1:2000SEP08
1445465H1
53
322


90
LG:1053229.1:2000SEP08
1259655
1
217


90
LG:1053229.1:2000SEP08
g1439745
13
308


90
LG:1053229.1:2000SEP08
6103338H1
66
376


90
LG:1053229.1:2000SEP08
1415866T6
393
587


90
LG:1053229.1:2000SEP08
g1442104
1
292


91
LG:248364.1:2000SEP08
7363704H1
621
1110


91
LG:248364.1:2000SEP08
7041822R8
693
1335


91
LG:248364.1:2000SEP08
7468175H1
456
898


91
LG:248364.1:2000SEP08
6758436H1
1100
1572


91
LG:248364.1:2000SEP08
6353449F7
1048
1595


91
LG:248364.1:2000SEP08
6608287H1
1244
1796


91
LG:248364.1:2000SEP08
7754413H1
1124
1659


91
LG:248364.1:2000SEP08
814363R1
1500
1930


91
LG:248364.1:2000SEP08
814363R6
1500
1854


91
LG:248364.1:2000SEP08
5047370H1
1447
1737


91
LG:248364.1:2000SEP08
7608161J1
1374
1930


91
LG:248364.1:2000SEP08
3071079H1
1364
1661


91
LG:248364.1:2000SEP08
g3931760
1512
1907


91
LG:248364.1:2000SEP08
814363H1
1500
1729


91
LG:248364.1:2000SEP08
7092325H1
146
384


91
LG:248364.1:2000SEP08
6567819H1
146
688


91
LG:248364.1:2000SEP08
6567819F6
146
606


91
LG:248364.1:2000SEP08
6776971J1
1
596


91
LG:248364.1:2000SEP08
93873143
220
416


91
LG:248364.1:2000SEP08
g1067627
187
516


91
LG:248364.1:2000SEP08
g6575611
182
600


91
LG:248364.1:2000SEP08
g3734235
180
494


91
LG:248364.1:2000SEP08
7608161H1
805
1211


91
LG:248364.1:2000SEP08
7384566H1
843
1160


91
LG:248364.1:2000SEP08
7097046H1
1009
1496


92
LG:477130.1:2000SEP08
5910620H1
1
302


92
LG:477130.1:2000SEP08
5910620F8
1
460


92
LG:477130.1:2000SEP08
5910668H1
2
301


92
LG:477130.1:2000SEP08
5910620T9
280
764


92
LG:477130.1:2000SEP08
5910620T6
480
889


93
LG:113786.17:2000SEP08
2441606F6
1
496


93
LG:113786.17:2000SEP08
2441606H1
1
218


93
LG:113786.17:2000SEP08
2472557H1
33
262


93
LG:113786.17:2000SEP08
2472557F6
33
395


94
LG:347635.1:2000SEP08
5639879H1
58
292


94
LG:347635.1:2000SEP08
5639879F6
58
586


94
LG:347635.1:2000SEP08
7186104H1
1
542


94
LG:347635.1:2000SEP08
g2359789
585
1021


94
LG:347635.1:2000SEP08
7714779H1
677
1165


94
LG:347635.1:2000SEP08
g274093
691
991


94
LG:347635.1:2000SEP08
5699927F6
1064
1517


94
LG:347635.1:2000SEP08
g2743365
457
916


94
LG:347635.1:2000SEP08
7152112H1
582
1003


94
LG:347635.1:2000SEP08
6777521J1
235
837


94
LG:347635.1:2000SEP08
7714779J1
23
594


94
LG:347635.1:2000SEP08
7757195J1
1
542


94
LG:347635.1:2000SEP08
7757195H1
89
667


94
LG:347635.1:2000SEP08
5699927H1
1065
1313


95
LG:242966.4:2000SEP08
568455H1
1669
1916


95
LG:242966.4:2000SEP08
2512929T6
1690
1934


95
LG:242966.4:2000SEP08
2196270H1
1716
1926


95
LG:242966.4:2000SEP08
1660835H1
1719
1939


95
LG:242966.4:2000SEP08
1538251H1
1742
1964


95
LG:242966.4:2000SEP08
600839H1
1755
2010


95
LG:242966.4:2000SEP08
039755H1
1920
2026


95
LG:242966.4:2000SEP08
g3329925
1786
1973


95
LG:242966.4:2000SEP08
g2524293
1878
1941


95
LG:242966.4:2000SEP08
g6133327
1668
1982


95
LG:242966.4:2000SEP08
1417037H1
1658
1903


95
LG:242966.4:2000SEP08
1417037F6
1658
2026


95
LG:242966.4:2000SEP08
2597301T6
1602
1937


95
LG:242966.4:2000SEP08
983791H1
1606
1903


95
LG:242966.4:2000SEP08
g6701826
1609
1973


95
LG:242966.4:2000SEP08
1383448T6
1610
1933


95
LG:242966.4:2000SEP08
3282241H1
1628
1865


95
LG:242966.4:2000SEP08
5098821H1
1634
1895


95
LG:242966.4:2000SEP08
g4648103
1652
1973


95
LG:242966.4:2000SEP08
g5836941
1652
1973


95
LG:242966.4:2000SEP08
g5741352
1652
1977


95
LG:242966.4:2000SEP08
5817026H1
1524
1697


95
LG:242966.4:2000SEP08
g173.4258
1550
1642


95
LG:242966.4:2000SEP08
477616R7
309
763


95
LG:242966.4:2000SEP08
7766841J2
338
939


95
LG:242966.4:2000SEP08
7763806H1
469
1087


95
LG:242966.4:2000SEP08
g2009268
496
708


95
LG:242966.4:2000SEP08
867326H1
504
762


95
LG:242966.4:2000SEP08
2180603F6
515
955


95
LG:242966.4:2000SEP08
2180603H1
515
800


95
LG:242966.4:2000SEP08
3344274H1
566
824


95
LG:242966.4:2000SEP08
7262796H1
1
524


95
LG:242966.4:2000SEP08
7633839J1
55
559


95
LG:242966.4:2000SEP08
6699726H1
189
550


95
LG:242966.4:2000SEP08
477616H1
309
570


95
LG:242966.4:2000SEP08
6420668H1
214
388


95
LG:242966.4:2000SEP08
2159734H1
277
500


95
LG:242966.4:2000SEP08
784416H1
286
603


95
LG:242966.4:2000SEP08
7677844H1
1485
1957


95
LG:242966.4:2000SEP08
1403054H1
1479
1725


95
LG:242966.4:2000SEP08
1403054F6
1479
1859


95
LG:242966.4:2000SEP08
6769563J1
1497
1981


95
LG:242966.4:2000SEP08
2490413H1
1506
1745


95
LG:242966.4:2000SEP08
2180603T6
1509
1931


95
LG:242966.4:2000SEP08
5817345H1
1522
1748


95
LG:242966.4:2000SEP08
1475794R6
1281
1636


95
LG:242966.4:2000SEP08
6352941F7
1403
1879


95
LG:242966.4:2000SEP08
1475794H1
1281
1459


95
LG:242966.4:2000SEP08
3016785H1
1414
1708


95
LG:242966.4:2000SEP08
2489244T6
1290
1789


95
LG:242966.4:2000SEP08
756332H1
1301
1559


95
LG:242966.4:2000SEP08
7766841H1
1308
1587


95
LG:242966.4:2000SEP08
1543702H1
1308
1491


95
LG:242966.4:2000SEP08
47761617
1357
1905


95
LG:242966.4:2000SEP08
1475794T6
1371
1921


95
LG:242966.4:2000SEP08
2760146H1
1376
1648


95
LG:242966.4:2000SEP08
6352941F8
1417
2023


95
LG:242966.4:2000SEP08
6512741H1
1446
1589


95
LG:242966.4:2000SEP08
7696070H1
1376
1565


95
LG:242966.4:2000SEP08
7035051H1
1391
1964


95
LG:242966.4:2000SEP08
2491496H1
1960
2026


95
LG:242966.4:2000SEP08
2891711H1
613
884


95
LG:242966.4:2000SEP08
2597301H1
1246
1515


95
LG:242966.4:2000SEP08
3223664H1
632
893


95
LG:242966.4:2000SEP08
6937623H1
757
1032


95
LG:242966.4:2000SEP08
6300077H1
835
1118


95
LG:242966.4:2000SEP08
2860363H1
881
1149


95
LG:242966.4:2000SEP08
7763806J1
887
1510


95
LG:242966.4:2000SEP08
2519487H1
945
1116


95
LG:242966.4:2000SEP08
1572340H1
1134
1316


95
LG:242966.4:2000SEP08
1507445H1
1146
1318


95
LG:242966.4:2000SEP08 4635969H1
1184
1419


95
LG:242966.4:2000SEP08
2597301F6
1246
1631


95
LG:242966.4:2000SEP08
4599922H1
1564
1843


95
LG:242966.4:2000SEP08
g5527462
1579
1973


95
LG:242966.4:2000SEP08
g4875402
1581
1981


95
LG:242966.4:2000SEP08
g3329924
1584
1973


95
LG:242966.4:2000SEP08
g5527471
1585
1973


95
LG:242966.4:2000SEP08
7128343H2
1597
1970


96
LG:217814.1:2000SEP08
2203116F6
1355
1841


96
LG:217814.1:2000SEP08
2203116T6
1344
1838


96
LG:217814.1:2000SEP08
6803273H1
1060
1530


96
LG:217814.1:2000SEP08
g1147087
1022
1386


96
LG:217814.1:2000SEP08
g2563845
1406
1815


96
LG:217814.1:2000SEP08
g2590584
1415
1826


96
LG:217814.1:2000SEP08
2203116H1
1355
1611


96
LG:217814.1:2000SEP08
2203035H1
1355
1590


96
LG:217814.1:2000SEP08
g1324443
1621
1842


96
LG:217814.1:2000SEP08
g3245150
1601
2005


96
LG:217814.1:2000SEP08
g4083193
1423
1820


96
LG:217814.1:2000SEP08
6900096F9
1
378


96
LG:217814.1:2000SEP08
6900096H1
1
449


96
LG:217814.1:2000SEP08
g4187748
1711
1784


96
LG:217814.1:2000SEP08
7283212H1
175
586


96
LG:217814.1:2000SEP08
3348991H1
239
394


96
LG:217814.1:2000SEP08
260602H1
254
571


96
LG:217814.1:2000SEP08
7720133H1
69
573


96
LG:217814.1:2000SEP08
7285913H1
746
1289


96
LG:217814.1:2000SEP08
7720133J1
424
968


97
LG:476452.1:2000SEP08
3953832H1
790
921


97
LG:476452.1:2000SEP08
6268518T8
564
1166


97
LG:476452.1:2000SEP08
5911995T6
566
1106


97
LG:476452.1:2000SEP08
5913343T9
598
1054


97
LG:476452.1:2000SEP08
5911995T9
541
1080


97
LG:476452.1:2000SEP08
6270538T8
562
1131


97
LG:476452.1:2000SEP08
6268518F8
1
642


97
LG:476452.1:2000SEP08
6270538H2
46
481


97
LG:476452.1:2000SEP08
6270538F8
46
443


97
LG:476452.1:2000SEP08
5913343F6
46
346


97
LG:476452.1:2000SEP08
5913343H1
46
293


97
LG:476452.1:2000SEP08
5911995F8
24
530


97
LG:476452.1:2000SEP08
5911995H1
24
305


97
LG:476452.1:2000SEP08
5913343F8
46
581


97
LG:476452.1:2000SEP08
6268518H1
46
562


97
LG:476452.1:2000SEP08
5911995F6
24
346


98
LG:1100657.1:2000SEP08
6795168F8
1
509


98
LG:1100657.1:2000SEP08
6797477H1
7
464


98
LG:1100657.1:2000SEP08
6798453T8
217
481


98
LG:1100657.1:2000SEP08
6793139H1
270
588


98
LG:1100657.1:2000SEP08
679313918
270
486


98
LG:1100657.1:2000SEP08
6793139F8
270
588


98
LG:1100657.1:2000SEP08
6798453H1
1
327


98
LG:1100657.1:2000SEP08
6795168H1
1
311


98
LG:1100657.1:2000SEP08
6798453F8
1579


98
LG:1100657.1:2000SEP08
6797477T8
7
485


98
LG:1100657.1:2000SEP08
6797477F8
7
544


99
LG:1132418.2:2000SEP08
6615330H1
1
440


100
LG:1098570.1:2000SEP08
6792174F8
1
574


100
LG:1098570.1:2000SEP08
6792174T8
2
612


100
LG:1098570.1:2000SEP08
6792174H1
1
566


101
LG:1097987.1:2000SEP08
1445774F7
415
986


101
LG:1097987.1:2000SEP08
2268189R6
132
526


101
LG:1097987.1:2000SEP08
7680579H1
1
617


101
LG:1097987.1:2000SEP08
2268189T6
481
1032


101
LG:1097987.1:2000SEP08
2268189H1
132
378


101
LG:1097987.1:2000SEP08
144577417
515
966


101
LG:1097987.1:2000SEP08
368103H1
667
910


101
LG:1097987.1:2000SEP08
7680579J1
386
930


101
LG:1097987.1:2000SEP08
1445774H1
409
654


101
LG:1097987.1:2000SEP08
g2328398
755
1076


101
LG:1097987.1:2000SEP08
2322571H1
837
1070


102
LG:337818.2:2000SEP08
6883053H1
527
1106


102
LG:337818.2:2000SEP08
6576957H1
1907
2455


102
LG:337818.2:2000SEP08
3254138H1
1908
2115


102
LG:337818.2:2000SEP08
5946104H1
1910
2145


102
LG:337818.2:2000SEP08
7748294H1
1911
2424


102
LG:337818.2:2000SEP08
5038396H1
1888
2146


102
LG:337818.2:2000SEP08
6820526H1
422
747


102
LG:337818.2:2000SEP08
6820526J1
422
747


102
LG:337818.2:2000SEP08
7710749J1
46
700


102
LG:337818.2:2000SEP08
4516041H1
1817
2066


102
LG:337818.2:2000SEP08
4180584H1
1872
2122


102
LG:337818.2:2000SEP08
g1968950
1886
2368


102
LG:337818.2:2000SEP08
1272843H1
1
245


102
LG:337818.2:2000SEP08
1274319H1
21
218


102
LG:337818.2:2000SEP08
2598183H1
24
263


102
LG:337818.2:2000SEP08
3256051H1
25
268


102
LG:337818.2:2000SEP08
2598183F6
31
607


102
LG:337818.2:2000SEP08
6826541J1
33
663


102
LG:337818.2:2000SEP08
6823903H1
34
188


102
LG:337818.2:2000SEP08
7218761H1
35
559


102
LG:337818.2:2000SEP08
7719403H1
46
603


102
LG:337818.2:2000SEP08
6786878H2
43
184


102
LG:337818.2:2000SEP08
1889107H1
1542
1812


102
LG:337818.2:2000SEP08
1889107F6
1542
1892


102
LG:337818.2:2000SEP08
6725031H1
1675
2299


102
LG:337818.2:2000SEP08
6823952J1
1549
2162


102
LG:337818.2:2000SEP08
5307668H1
1567
1691


102
LG:337818.2:2000SEP08
5840503H2
1578
1835


102
LG:337818.2:2000SEP08
4519262H1
2360
2599


102
LG:337818.2:2000SEP08
1272843T6
2368
2562


102
LG:337818.2:2000SEP08
6104909H1
2413
2604


102
LG:337818.2:2000SEP08
5056523H1
2466
2604


102
LG:337818.2:2000SEP08
g5038163
2168
2608


102
LG:337818.2:2000SEP08
g3146568
2200
2604


102
LG:337818.2:2000SEP08
g2355286
2200
2589


102
LG:337818.2:2000SEP08
1845337T6
2212
2566


102
LG:337818.2:2000SEP08
1845337H1
2212
2433


102
LG:337818.2:2000SEP08
1845337R6
2212
2562


102
LG:337818.2:2000SEP08
g4288591
2215
2599


102
LG:337818.2:2000SEP08
g5659132
2219
2551


102
LG:337818.2:2000SEP08
913114H1
2228
2509


102
LG:337818.2:2000SEP08
g1960980
2253
2604


102
LG:337818.2:2000SEP08
g5887689
2244
2601


102
LG:337818.2:2000SEP08
2700155F6
1922
2433


102
LG:337818.2:2000SEP08
2700155H1
1922
2121


102
LG:337818.2:2000SEP08
2061567T6
1951
2554


102
LG:337818.2:2000SEP08
3365965H1
1983
2108


102
LG:337818.2:2000SEP08
g5591869
2006
2220


102
LG:337818.2:2000SEP08
1749882T6
2039
2571


102
LG:337818.2:2000SEP08
1752020H1
2049
2258


102
LG:337818.2:2000SEP08
2700155T6
2063
2563


102
LG:337818.2:2000SEP08
1889107T6
2099
2562


102
LG:337818.2:2000SEP08
3236592H2
2125
2340


102
LG:337818.2:2000SEP08
5291302H1
2152
2398


102
LG:337818.2:2000SEP08
g5838009
2250
2611


102
LG:337818.2:2000SEP08
911966H1
2249
2503


102
LG:337818.2:2000SEP08
g5913083
2251
2604


102
LG:337818.2:2000SEP08
g3741346
2254
2611


102
LG:337818.2:2000SEP08
g3785022
2297
2602


102
LG:337818.2:2000SEP08
g2463906
2312
2607


102
LG:337818.2:2000SEP08
g4312734
2347
2599


102
LG:337818.2:2000SEP08
g2100983
2358
2591


102
LG:337818.2:2000SEP08
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1
331


102
LG:337818.2:2000SEP08
1272843F6
1
593


102
LG:337818.2:2000SEP08
2061567R6
1698
2177


102
LG:337818.2:2000SEP08
2061567H1
1698
1970


102
LG:337818.2:2000SEP08
4399331H1
1734
2000


102
LG:337818.2:2000SEP08
4399135H1
1734
1991


102
LG:337818.2:2000SEP08
2250985H1
1734
1964


102
LG:337818.2:2000SEP08
1501428H1
1737
1930


102
LG:337818.2:2000SEP08
6018675H1
1812
2378


102
LG:337818.2:2000SEP08
7713423J1
1483
2070


102
LG:337818.2:2000SEP08
794690H1
1496
1698


102
LG:337818.2:2000SEP08
6576416H1
1513
1850


102
LG:337818.2:2000SEP08
476160H1
1389
1655


102
LG:337818.2:2000SEP08
6158833H1
1433
1523


102
LG:337818.2:2000SEP08
4552488H1
958
1120


102
LG:337818.2:2000SEP08
7219413H1
999
1496


102
LG:337818.2:2000SEP08
4243388H1
919
1251


102
LG:337818.2:2000SEP08
g713204
1029
1191


102
LG:337818.2:2000SEP08
g1967839
1091
1429


102
LG:337818.2:2000SEP08
7680157J1
1174
1775


102
LG:337818.2:2000SEP08
7675304J1
1177
1790


102
LG:337818.2:2000SEP08
7680157H1
956
1465


102
LG:337818.2:2000SEP08
7710749H1
1261
1790


102
LG:337818.2:2000SEP08
3737077H1
1295
1453


102
LG:337818.2:2000SEP08
6326476H1
1313
1610


102
LG:337818.2:2000SEP08
g1968949
1345
1812


102
LG:337818.2:2000SEP08
g2229641
1360
1792


102
LG:337818.2:2000SEP08
7713423H1
664
1234


102
LG:337818.2:2000SEP08
7719403J1
528
1194


102
LG:337818.2:2000SEP08
6826541H1
672
1240


102
LG:337818.2:2000SEP08
7634622J1
718
1162


102
LG:337818.2:2000SEP08
7634622H1
720
1162


102
LG:337818.2:2000SEP08
3857549H1
797
1106


102
LG:337818.2:2000SEP08
1749882H1
811
1085


102
LG:337818.2:2000SEP08
1749882F6
811
1171


102
LG:337818.2:2000SEP08
7675304H1
658
1121


102
LG:337818.2:2000SEP08
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860
1357


102
LG:337818.2:2000SEP08
7746862H1
873
1313


102
LG:337818.2:2000SEP08
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885
986


102
LG:337818.2:2000SEP08
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885
1086


102
LG:337818.2:2000SEP08
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893
1370


102
LG:337818.2:2000SEP08
2271032H1
893
1152


102
LG:337818.2:2000SEP08
7128738H1
913
1433


103
LG:1040582.1:2000SEP08
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2
321


103
LG:1040582.1:2000SEP08
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1
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103
LG:1040582.1:2000SEP08
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220
660


103
LG:1040582.1:2000SEP08
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249
548


104
LG:1099122.1:2000SEP08
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13
405


104
LG:1099122.1:2000SEP08
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2
425


104
LG:1099122.1:2000SEP08
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14
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104
LG:1099122.1:2000SEP08
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1
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104
LG:1099122.1:2000SEP08
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1
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104
LG:1099122.1:2000SEP08
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138
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104
LG:1099122.1:2000SEP08
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14
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104
LG:1099122.1:2000SEP08
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15
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105
LG:1327449.1:2000SEP08
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1
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105
LG:1327449.1:2000SEP08
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1
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105
LG:1327449.1:2000SEP08
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233
564


105
LG:1327449.1:2000SEP08
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338
553


105
LG:1327449.1:2000SEP08
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418
595


105
LG:1327449.1:2000SEP08
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497
596


106
LG:227933.5:2000SEP08
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183
820


106
LG:227933.5:2000SEP08
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1
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106
LG:227933.5:2000SEP08
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1
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106
LG:227933.5:2000SEP08
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7
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106
LG:227933.5:2000SEP08
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301
820


106
LG:227933.5:2000SEP08
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113
702


106
LG:227933.5:2000SEP08
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1017
1350


106
LG:227933.5:2000SEP08
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1114
1369


106
LG:227933.5:2000SEP08
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1114
1457


106
LG:227933.5:2000SEP08
008680H1
1221
1504


106
LG:227933.5:2000SEP08
4163591H1
1276
1576


106
LG:227933.5:2000SEP08
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303
862


106
LG:227933.5:2000SEP08
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305
598


106
LG:227933.5:2000SEP08
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306
589


106
LG:227933.5:2000SEP08
6859841H1
337
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106
LG:227933.5:2000SEP08
3618330H1
468
766


106
LG:227933.5:2000SEP08
2984273H1
469
731


106
LG:227933.5:2000SEP08
6476227H1
634
1170


106
LG:227933.5:2000SEP08
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837
1213


106
LG:227933.5:2000SEP08
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838
1281


106
LG:227933.5:2000SEP08
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837
1127


106
LG:227933.5:2000SEP08
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838
1344


106
LG:227933.5:2000SEP08
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869
1118


107
LG:1043709.2:2000SEP08
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1
431


107
LG:1043709.2:2000SEP08
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151
780


108
LG:1099871.1:2000SEP08
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1
560


108
LG:1099871.1:2000SEP08
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503
673


108
LG:1099871.1:2000SEP08
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1
667


108
LG:1099871.1:2000SEP08
g1626426
479
656


108
LG:1099871.1:2000SEP08
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1
556


108
LG:1099871.1:2000SEP08
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1
437


108
LG:1099871.1:2000SEP08
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1 284


108
LG:1099871.1:2000SEP08
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1
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109
LG:1399139.4:2000SEP08
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342
607


109
LG:1399139.4:2000SEP08
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539
601


109
LG:1399139.4:2000SEP08
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192
601


109
LG:1399139.4:2000SEP08
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397
558


109
LG:1399139.4:2000SEP08
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1
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109
LG:1399139.4:2000SEP08
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309
408


109
LG:1399139.4:2000SEP08
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342
783


109
LG:1399139.4:2000SEP08
g2113065
354
676


109
LG:1399139.4:2000SEP08
6215226H1
221
670


110
LG:236386.1:2000SEP08
6317150H1
3421
3711


110
LG:236386.1:2000SEP08
6317128H1
3421
3548


110
LG:236386.1:2000SEP08
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3421
3702


110
LG:236386.1:2000SEP08
2661806T6
3447
3843


110
LG:236386.1:2000SEP08
g3429071
3462
3880


110
LG:236386.1:2000SEP08
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3472
3886


110
LG:236386.1:2000SEP08
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3492
3875


110
LG:236386.1:2000SEP08
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3502
3880


110
LG:236386.1:2000SEP08
2878117H1
3505
3776


110
LG:236386.1:2000SEP08
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3511
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110
LG:236386.1:2000SEP08
6325947H1
3421
3714


110
LG:236386.1:2000SEP08
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3405
3669


110
LG:236386.1:2000SEP08
4333836H1
3394
3671


110
LG:236386.1:2000SEP08
840648H1
3394
3640


110
LG:236386.1:2000SEP08
2615527H1
2645
2897


110
LG:236386.1:2000SEP08
1438880H1
2708
2980


110
LG:236386.1:2000SEP08
1438876H1
2708
2978


110
LG:236386.1:2000SEP08
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2708
3074


110
LG:236386.1:2000SEP08
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2952
3200


110
LG:236386.1:2000SEP08
2258046H1
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2973


110
LG:236386.1:2000SEP08
7735093H1
2980
3603


110
LG:236386.1:2000SEP08
6479471H1
2806
3340


110
LG:236386.1:2000SEP08
7054594H1
2816
3383


110
LG:236386.1:2000SEP08
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3022
3195


110
LG:236386.1:2000SEP08
5274874H
12848
3075


110
LG:236386.1:2000SEP08
2857322H1
2920
3177


110
LG:236386.1:2000SEP08
792748H1
2924
3151


110
LG:236386.1:2000SEP08
793130H1
2925
3131


110
LG:236386.1:2000SEP08
792748R1
2925
3509


110
LG:236386.1:2000SEP08
7159471H1
2934
3484


110
LG:236386.1:2000SEP08
1541872H1
2951
3157


110
LG:236386.1:2000SEP08
6559394H1
1836
2450


110
LG:236386.1:2000SEP08
6553230H1
1836
2188


110
LG:236386.1:2000SEP08
3382113H1
1906
2113


110
LG:236386.1:2000SEP08
2272356H1
1647
1915


110
LG:236386.1:2000SEP08
2661806H1
2112
2383


110
LG:236386.1:2000SEP08
2661806F6
2112
2553


110
LG:236386.1:2000SEP08
g6476309
2172
2528


110
LG:236386.1:2000SEP08
2627073H1
2183
2413


110
LG:236386.1:2000SEP08
2627315H1
2183
2411


110
LG:236386.1:2000SEP08
3901711H1
2270
2513


110
LG:236386.1:2000SEP08
5763849H1
2373
2890


110
LG:236386.1:2000SEP08
7256511H1
2420
2921


110
LG:236386.1:2000SEP08
3572311H1
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2721


110
LG:236386.1:2000SEP08
3572311F6
2509
3086


110
LG:236386.1:2000SEP08
7336064H1
2549
2991


110
LG:236386.1:2000SEP08
2272356T6
2588
3010


110
LG:236386.1:2000SEP08
685902H1
2627
2848


110
LG:236386.1:2000SEP08
6831490J1
496
688


110
LG:236386.1:2000SEP08
6831490H1
496
688


110
LG:236386.1:2000SEP08
7738646H1
755
1252


110
LG:236386.1:2000SEP08
6938224H1
973
1366


110
LG:236386.1:2000SEP08
7267489H1
1082
1603


110
LG:236386.1:2000SEP08
g3888759
1148
1514


110
LG:236386.1:2000SEP08
6454789H1
1317
1820


110
LG:236386.1:2000SEP08
684735H1
1380
1626


110
LG:236386.1:2000SEP08
7649660H2
1420
2039


110
LG:236386.1:2000SEP08
6952285H1
1506
2072


110
LG:236386.1:2000SEP08
4458494F6
1519
1967


110
LG:236386.1:2000SEP08
4458494H1
1520
1755


110
LG:236386.1:2000SEP08
7255931H2
1596
1777


110
LG:236386.1:2000SEP08
6909665J1
1633
2177


110
LG:236386.1:2000SEP08
2272356R6
1647
1966


110
LG:236386.1:2000SEP08
4181419H1
1
220


110
LG:236386.1:2000SEP08
6779195J1
119
758


110
LG:236386.1:2000SEP08
113399R6
483
847


110
LG:236386.1:2000SEP08
5104505H1
3515
3738


110
LG:236386.1:2000SEP08
g4081742
3517
3883


110
LG:236386.1:2000SEP08
1452312T6
3521
3836


110
LG:236386.1:2000SEP08
g898312
3538
3878


110
LG:236386.1:2000SEP08
6499719H1
3537
3869


110
LG:236386.1:2000SEP08
g4081564
3538
3883


110
LG:236386.1:2000SEP08
g2335900
3571
3880


110
LG:236386.1:2000SEP08
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3573
3875


110
LG:236386.1:2000SEP08
g1521304 3576
3891


110
LG:236386.1:2000SEP08
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3577
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110
LG:236386.1:2000SEP08
5790863H 1
3580
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110
LG:236386.1:2000SEP08 5787849H1
3580
3875


110
LG:236386.1:2000SEP08 5789451H1
3580
3858


110
LG:236386.1:2000SEP08
p5528373
3592
3880


110
LG:236386.1:2000SEP08
p1516463
3595
3891


110
LG:236386.1:2000SEP08
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3628
3880


110
LG:236386.1:2000SEP08
344685H1
3641
3882


110
LG:236386.1:2000SEP08
389997H1
3639
3875


110
LG:236386.1:2000SEP08
6357624H 1
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3882


110
LG:236386.1:2000SEP08
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3652
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110
LG:236386.1:2000SEP08
p6477150
3654
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110
LG:236386.1:2000SEP08
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3661
3883


110
LG:236386.1:2000SEP08
1689958H1
3661
3867


110
LG:236386.1:2000SEP08
1 689958T6
3666
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110
LG:236386.1:2000SEP08
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3684
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110
LG:236386.1:2000SEP08
357231 1T6
3705
3832


110
LG:236386.1:2000SEP08
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3752
3875


110
LG:236386.1:2000SEP08
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3298
3562


110
LG:236386.1:2000SEP08
1320150H1
3124
3347


110
LG:236386.1:2000SEP08
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3126
3401


110
LG:236386.1:2000SEP08
5379052H1
3134
3346


110
LG:236386.1:2000SEP08
3406784H1
3142
3390


110
LG:236386.1:2000SEP08
2527855H1
3172
3504


110
LG:236386.1:2000SEP08
g1521303
3191
3623


110
LG:236386.1:2000SEP08
p1517127
3191
3666


110
LG:236386.1:2000SEP08
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3205
3428


110
LG:236386.1:2000SEP08
2414749F6
3208
3714


110
LG:236386.1:2000SEP08
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3207
3498


110
LG:236386.1:2000SEP08
2414751H1
3208
3467


110
LG:236386.1:2000SEP08
2414483H1
3208
3432


110
LG:236386.1:2000SEP08
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3262
3865


110
LG:236386.1:2000SEP08
p898311
3269
3438


110
LG:236386.1:2000SEP08
1452312F1
3275
3796


110
LG:236386.1:2000SEP08
1452312F6
3275
3702


110
LG:236386.1:2000SEP08
1452312H1
3275
3534


110
LG:236386.1:2000SEP08
3011048H1
3326
3611


110
LG:236386.1:2000SEP08
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3334
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110
LG:236386.1:2000SEP08
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3335
3606


110
LG:236386.1:2000SEP08
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3027
3331


110
LG:236386.1:2000SEP08
7649660J2
3034
3668


110
LG:236386.1:2000SEP08
1702166F6
3047
3541


110
LG:236386.1:2000SEP08
1702166H1
3047
3258


110
LG:236386.1:2000SEP08
4980587H1
3060
3313


110
LG:236386.1:2000SEP08
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3076
3593


110
LG:236386.1:2000SEP08
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3079
3376


110
LG:236386.1:2000SEP08
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3078
3366


110
LG:236386.1:2000SEP08
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3082
3273


110
LG:236386.1:2000SEP08
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3097
3383


110
LG:236386.1:2000SEP08
4880465H1
3100
3335


110
LG:236386.1:2000SEP08
2658395H1
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4210


110
LG:236386.1:2000SEP08
4099042H2
3777
3887


110
LG:236386.1:2000SEP08
1243554H1
3777
3883


110
LG:236386.1:2000SEP08
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3782
4137


110
LG:236386.1:2000SEP08
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4131


110
LG:236386.1:2000SEP08
g4325490
3795
3875


110
LG:236386.1:2000SEP08
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110
LG:236386.1:2000SEP08
2623608H1
3349
3576


110
LG:236386.1:2000SEP08
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3394
3875


111
LG:1015157.1:2000SEP08
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638


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LG:1015157.1:20003EP08
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2
438


111
LG:1015157.1:2000SEP08
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175
658


112
LG:1065433.1:2000SEP08
4023626H1
701
980


112
LG:1065433.1:2000SEP08
4216384H1
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112
LG:1065433.1:2000SEP08
3449946H1
1
233


112
LG:1065433.1:2000SEP08
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317
911


112
LG:1065433.1:2000SEP08
421638.4F6
563
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112
LG:1065433.1:2000SEP08
3449946R6
1
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113
LG:236992.4:2000SEP08
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LG:236992.4:2000SEP08
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LG:236992.4:2000SEP08
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LG:236992.4:2000SEP08
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LG:236992.4:2000SEP08
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114
LG:1071124.1:2000SEP08
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114
LG:1071124.1:2000SEP08
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LG:1071124.1:2000SEP08
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114
LG:1071124.1:2000SEP08
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LG:1071124.1:2000SEP08
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114
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114
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114
LG:1071124.1:2000SEP08
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114
LG:1071124.1:2000SEP08
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114
LG:1071124.1:2000SEP08
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114
LG:1071124.1:2000SEP08
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LG:1071124.1:2000SEP08
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114
LG:1071124.1:2000SEP08
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115
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LG:206425.2:2000SEP08
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115
LG:206425.2:2000SEP08
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LG:206425.2:2000SEP08
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LG:206425.2:2000SEP08
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LG:206425.2:2000SEP08
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115
LG:206425.2:2000SEP08
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LG:206425.2:2000SEP08
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115
LG:206425.2:2000SEP08
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LG:206425.2:2000SEP08
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LG:206425.2:2000SEP08
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115
LG:206425.2:2000SEP08
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115
LG:206425.2:2000SEP08
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LG:206425.2:2000SEP08
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LG:206425.2:2000SEP08
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LG:206425.2:2000SEP08
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115
LG:206425.2:2000SEP08
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LG:206425.2:2000SEP08
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LG:206425.2:2000SEP08
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LG:206425.2:2000SEP08
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LG:206425.2:2000SEP08
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LG:206425.2:2000SEP08
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LG:206425.2:2000SEP08
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115
LG:206425.2:2000SEP08
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115
LG:206425.2:2000SEP08
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1588
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115
LG:206425.2:2000SEP08
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115
LG:206425.2:2000SEP08
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115
LG:206425.2:2000SEP08
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LG:206425.2:2000SEP08
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115
LG:206425.2:2000SEP08
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115
LG:206425.2:2000SEP08
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115
LG:206425.2:2000SEP08
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115
LG:206425.2:2000SEP08
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2000


115
LG:206425.2:2000SEP08
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1817
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116
LG:885747.2:2000SEP08
6072957T8
1
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117
LG:1140501.1:2000SEP08
2266814H1
1037
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117
LG:1140501.1:2000SEP08
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117
LG:1140501.1:2000SEP08
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117
LG:1140501.1:2000SEP08
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117
LG:1140501.1:2000SEP08
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117
LG:1140501.1:2000SEP08
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117
LG:1140501.1:2000SEP08
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117
LG:1140501.1:2000SEP08
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117
LG:1140501.1:2000SEP08
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117
LG:1140501.1:2000SEP08
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117
LG:1140501.1:2000SEP08
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117
LG:1140501.1:2000SEP08
g6133150
1269
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117
LG:1140501.1:2000SEP08
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117
LG:1140501.1:2000SEP08
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117
LG:1140501.1:2000SEP08
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1288
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117
LG:1140501.1:2000SEP08
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1294
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117
LG:1140501.1:2000SEP08
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1304
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117
LG:1140501.1:2000SEP08
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1306
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117
LG:1140501.1:2000SEP08
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117
LG:1140501.1:2000SEP08
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1325
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117
LG:1140501.1:2000SEP08
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117
LG:1140501.1:2000SEP08
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1328
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117
LG:1140501.1:2000SEP08
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1329
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117
LG:1140501.1:2000SEP08
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1328
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117
LG:1140501.1:2000SEP08
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1345
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117
LG:1140501.1:2000SEP08
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1346
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117
LG:1140501.1:2000SEP08
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1349
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117
LG:1140501.1:2000SEP08
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1350
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117
LG:1140501.1:2000SEP08
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1358
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117
LG:1140501.1:2000SEP08
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1358
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117
LG:1140501.1:2000SEP08
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1363
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117
LG:1140501.1:2000SEP08
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1380
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117
LG:1140501.1:2000SEP08
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1379
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117
LG:1140501.1:2000SEP08
g1198673
1379
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117
LG:1140501.1:2000SEP08
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1389
1729


117
LG:1140501.1:2000SEP08
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1389
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117
LG:1140501.1:2000SEP08
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117
LG:1140501.1:2000SEP08
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117
LG:1140501.1:2000SEP08
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1411
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117
LG:1140501.1:2000SEP08
3714610H1
1411
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117
LG:1140501.1:2000SEP08
2564520H1
1415
1673


117
LG:1140501.1:2000SEP08
1941138H1
1602
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117
LG:1140501.1:2000SEP08
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1522
1712


117
LG:1140501.1:2000SEP08
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1534
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117
LG:1140501.1:2000SEP08
5371341H1
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117
LG:1140501.1:2000SEP08
g6301731
1581
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117
LG:1140501.1:2000SEP08
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1429
1712


117
LG:1140501.1:2000SEP08
g958393
1463
1681


117
LG:1140501.1:2000SEP08
g1801301
1499
1721


117
LG:1140501.1:2000SEP08
1501643H1
949
1109


117
LG:1140501.1:2000SEP08
4352981H1
949
1163


117
LG:1140501.1:2000SEP08
6861727H1
952
1442


117
LG:1140501.1:2000SEP08
2267642H1
957
1115


117
LG:1140501.1:2000SEP08
3332580H1
959
1212


117
LG:1140501.1:2000SEP08
751881H1
967
1145


117
LG:1140501.1:2000SEP08
1400206H1
967
1210


117
LG:1140501.1:2000SEP08
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971
1122


117
LG:1140501.1:2000SEP08
1720108H1
980
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117
LG:1140501.1:2000SEP08
g4152386
993
1430


117
LG:1140501.1:2000SEP08
1269892H1
988
1187


117
LG:1140501.1:2000SEP08
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1007
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117
LG:1140501.1:2000SEP08
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1
474


117
LG:1140501.1:2000SEP08
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47
279


117
LG:1140501.1:2000SEP08
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47
586


117
LG:1140501.1:2000SEP08
g1324442
98
361


117
LG:1140501.1:2000SEP08
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141
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117
LG:1140501.1:2000SEP08
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237
533


117
LG:1140501.1:2000SEP08
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300
369


117
LG:1140501.1:2000SEP08
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1007
1243


117
LG:1140501.1:2000SEP08
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1007
1237


117
LG:1140501.1:2000SEP08
036959H1
1013
1237


117
LG:1140501.1:2000SEP08
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477
911


117
LG:1140501.1:2000SEP08
1772758H1
1029
1287


117
LG:1140501.1:2000SEP08
7043093H1
477
1018


117
LG:1140501.1:2000SEP08
5197443H1
1034
1109


117
LG:1140501.1:2000SEP08
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477
909


117
LG:1140501.1:2000SEP08
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877
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117
LG:1140501.1:2000SEP08
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881
1024


117
LG:1140501.1:2000SEP08
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881
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117
LG:1140501.1:2000SEP08
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884
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117
LG:1140501.1:2000SEP08
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894
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117
LG:1140501.1:2000SEP08
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1037
1292


117
LG:1140501.1:2000SEP08
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918
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117
LG:1140501.1:2000SEP08
1596563H1
918
1038


117
LG:1140501.1:2000SEP08
1253123H1
928
1169


118
LG:001239.1:2000SEP08
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1901
2154


118
LG:001239.1:2000SEP08
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1349
1845


118
LG:001239.1:2000SEP08
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1805
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118
LG:001239.1:2000SEP08
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1380
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118
LG:001239.1:2000SEP08
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1452
1645


118
LG:001239.1:2000SEP08
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1552
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118
LG:001239.1:2000SEP08
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1699
1943


118
LG:001239.1:2000SEP08
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1804
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118
LG:001239.1:2000SEP08
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1071
1432


118
LG:001239.1:2000SEP08
g5554311
922
1240


118
LG:001239.1:2000SEP08
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964
1178


118
LG:001239.1:2000SEP08
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1030
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118
LG:001239.1:2000SEP08
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1070
1279


118
LG:001239.1:2000SEP08
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728
1332


118
LG:001239.1:2000SEP08
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884
1117


118
LG:001239.1:2000SEP08
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729
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118
LG:001239.1:2000SEP08
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729
960


118
LG:001239.1:2000SEP08
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1
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118
LG:001239.1:2000SEP08
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497
1028


118
LG:001239.1:2000SEP08
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540
1115


118
LG:001239.1:2000SEP08
7661635H1
548
1053


118
LG:001239.1:2000SEP08
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3
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118
LG:001239.1:2000SEP08
1912873H1
461
693


118
LG:001239.1:2000SEP08
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470
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118
LG:001239.1:2000SEP08
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1
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118
LG:001239.1:2000SEP08
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554
755


118
LG:001239.1:2000SEP08
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614
892


118
LG:001239.1:2000SEP08
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547
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118
LG:001239.1:2000SEP08
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552
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118
LG:001239.1:2000SEP08
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554
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118
LG:001239.1:2000SEP08
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541
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118
LG:001239.1:2000SEP08
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541
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119
LG:018980.1:2000SEP08
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731
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119
LG:018980.1:2000SEP08
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1
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119
LG:018980.1:2000SEP08
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723
1182


119
LG:018980.1:2000SEP08
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409
969


119
LG:018980.1:2000SEP08
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704
987


119
LG:018980.1:2000SEP08
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951
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119
LG:018980.1:2000SEP08
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951
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119
LG:018980.1:2000SEP08
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955
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119
LG:018980.1:2000SEP08
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33
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119
LG:018980.1:2000SEP08
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33
444


119
LG:018980.1:2000SEP08
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804
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119
LG:018980.1:2000SEP08
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351
831


119
LG:018980.1:2000SEP08
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134
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119
LG:018980.1:2000SEP08
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134
381


120
LG:1083120.3:2000SEP08
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133
385


120
LG:1083120.3:2000SEP08
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1
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120
LG:1083120.3:2000SEP08
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50
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121
LG:233258.3:2000SEP08
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4154
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121
LG:233258.3:2000SEP08
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4167
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121
LG:233258.3:2000SEP08
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4187
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121
LG:233258.3:2000SEP08
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4188
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121
LG:233258.3:2000SEP08
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4261
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121
LG:233258.3:2000SEP08
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4569
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121
LG:233258.3:2000SEP08
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4074
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121
LG:233258.3:2000SEP08
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4075
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121
LG:233258.3:2000SEP08
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4081
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121
LG:233258.3:2000SEP08
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4081
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121
LG:233258.3:2000SEP08
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4081
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121
LG:233258.3:2000SEP08
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4105
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121
LG:233258.3:2000SEP08
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4139
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121
LG:233258.3:2000SEP08
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4139
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121
LG:233258.3:2000SEP08
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4144
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121
LG:233258.3:2000SEP08
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4147
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121
LG:233258.3:2000SEP08
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3991
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121
LG:233258.3:2000SEP08
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4001
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121
LG:233258.3:2000SEP08
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4004
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121
LG:233258.3:2000SEP08
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4025
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121
LG:233258.3:2000SEP08
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4052
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121
LG:233258.3:2000SEP08
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4052
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121
LG:233258.3:2000SEP08
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4059
4329


121
LG:233258.3:2000SEP08
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4074
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121
LG:233258.3:2000SEP08
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4073
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121
LG:233258.3:2000SEP08
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4074
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121
LG:233258.3:2000SEP08
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4074
4329


121
LG:233258.3:2000SEP08
1651244T6
4011
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121
LG:233258.3:2000SEP08
1638434H1
4004
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121
LG:233258.3:2000SEP08
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4008
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121
LG:233258.3:2000SEP08
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4009
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121
LG:233258.3:2000SEP08
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1782
2079


121
LG:233258.3:2000SEP08
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1782
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121
LG:233258.3:2000SEP08
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1825
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121
LG:233258.3:2000SEP08
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1876
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121
LG:233258.3:2000SEP08
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1878
2117


121
LG:233258.3:2000SEP08
1651244F6
3093
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121
LG:233258.3:2000SEP08
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3093
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121
LG:233258.3:2000SEP08
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3111
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121
LG:233258.3:2000SEP08
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3114
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121
LG:233258.3:2000SEP08
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3143
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121
LG:233258.3:2000SEP08
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3143
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121
LG:233258.3:2000SEP08
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3160
3441


121
LG:233258.3:2000SEP08
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3771
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121
LG:233258.3:2000SEP08
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3773
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121
LG:233258.3:2000SEP08
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3789
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121
LG:233258.3:2000SEP08
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3794
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121
LG:233258.3:2000SEP08
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3809
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121
LG:233258.3:2000SEP08
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3811
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121
LG:233258.3:2000SEP08
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3771
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121
LG:233258.3:2000SEP08
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121
LG:233258.3:2000SEP08
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121
LG:233258.3:2000SEP08
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2960
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121
LG:233258.3:2000SEP08
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2994
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121
LG:233258.3:2000SEP08
3770483H1
2999
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121
LG:233258.3:2000SEP08
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3024
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121
LG:233258.3:2000SEP08
7260921H1
3027
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121
LG:233258.3:2000SEP08
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3081
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121
LG:233258.3:2000SEP08
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3086
3352


121
LG:233258.3:2000SEP08
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3087
3328


121
LG:233258.3:2000SEP08
1456075R1
3829
4335


121
LG:233258.3:2000SEP08
1427649T6
3846
4289


121
LG:233258.3:2000SEP08
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3818
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121
LG:233258.3:2000SEP08
1482987T6
3855
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121
LG:233258.3:2000SEP08
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3856
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19
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131
LG:1084051.1:2000SEP08
1895443H1
19
272


131
LG:1084051.1:2000SEP08
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86
235


131
LG:1084051.1:2000SEP08
3021710H1
568
853


131
LG:1084051.1:2000SEP08
3021038T6
568
880


131
LG:1084051.1:2000SEP08
3836068H1
7
289


132
LG:1082393.1:2000SEP08
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1189
1391


132
LG:1082393.1:2000SEP08
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1050
1590


132
LG:1082393.1:2000SEP08
4129281F6
1189
1637


132
LG:1082393.1:2000SEP08
2041133H1
1341
1576


132
LG:1082393.1:2000SEP08
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1357
1907


132
LG:1082393.1:2000SEP08
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1370
1963


132
LG:1082393.1:2000SEP08
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1407
1953


132
LG:1082393.1:2000SEP08
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1425
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132
LG:1082393.1:2000SEP08
4181819T8
1554
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132
LG:1082393.1:2000SEP08
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1570
2175


132
LG:1082393.1:2000SEP08
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1709
2206


132
LG:1082393.1:2000SEP08
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1048
1543


132
LG:1082393.1:2000SEP08
1691842H1
781
1020


132
LG:1082393.1:2000SEP08
5004434H1
1076
1286


132
LG:1082393.1:2000SEP08
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1
456


132
LG:1082393.1:2000SEP08
7740514H1
13
431


132
LG:1082393.1:2000SEP08
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35
590


132
LG:1082393.1:2000SEP08
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38
605


132
LG:1082393.1:2000SEP08
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46
456


132
LG:1082393.1:2000SEP08
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44
616


132
LG:1082393.1:2000SEP08
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47
452


132
LG:1082393.1:2000SEP08
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692


132
LG:1082393.1:2000SEP08
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365
733


132
LG:1082393.1:2000SEP08
774051411
409
1070


132
LG:1082393.1:2000SEP08
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518
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132
LG:1082393.1:2000SEP08
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558
783


132
LG:1082393.1:2000SEP08
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597
885


132
LG:1082393.1:2000SEP08
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597
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132
LG:1082393.1:2000SEP08
7626695H1
658
1192


132
LG:1082393.1:2000SEP08
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1048
1519


132
LG:1082393.1:2000SEP08
6051387J1
1662
2175


132
LG:1082393.1:2000SEP08
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8
619


132
LG:1082393.1:2000SEP08
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1252
1450


132
LG:1082393.1:2000SEP08
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453
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132
LG:1082393.1:2000SEP08
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132
LG:1082393.1:2000SEP08
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132
LG:1082393.1:2000SEP08
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8
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132
LG:1082393.1:2000SEP08
1691166H1
964
1056


132
LG:1082393.1:2000SEP08
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781
1380


132
LG:1082393.1:2000SEP08
6560051F8
697
1208


132
LG:1082393.1:2000SEP08
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1048
1620


132
LG:1082393.1:2000SEP08
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8
541


132
LG:1082393.1:2000SEP08
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855
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132
LG:1082393.1:2000SEP08
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1037
1621


132
LG:1082393.1:2000SEP08
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1134
1351


132
LG:1082393.1:2000SEP08
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1193
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132
LG:1082393.1:2000SEP08
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22
564


132
LG:1082393.1:2000SEP08
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1207
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132
LG:1082393.1:2000SEP08
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1037
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132
LG:1082393.1:2000SEP08
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1048
1543


132
LG:1082393.1:2000SEP08
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55
519


132
LG:1082393.1:2000SEP08
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8
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132
LG:1082393.1:2000SEP08
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1189
1440


132
LG:1082393.1:2000SEP08
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1226
1516


132
LG:1082393.1:2000SEP08
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697
1236


132
LG:1082393.1:2000SEP08
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104
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132
LG:1082393.1:2000SEP08
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49
608


132
LG:1082393.1:2000SEP08
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132
LG:1082393.1:2000SEP08
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132
LG:1082393.1:2000SEP08
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132
LG:1082393.1:2000SEP08
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464
1101


132
LG:1082393.1:2000SEP08
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181
590


132
LG:1082393.1:2000SEP08
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1048
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132
LG:1082393.1:2000SEP08
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885


132
LG:1082393.1:2000SEP08
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1037
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133
LG:1086183.1:2000SEP08
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308


133
LG:1086183.1:2000SEP08
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113
411


133
LG:1086183.1:2000SEP08
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1
399


133
LG:1086183.1:2000SEP08
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76
323


133
LG:1086183.1:2000SEP08
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103
368


133
LG:1086183.1:2000SEP08
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512
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133
LG:1086183.1:2000SEP08
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76
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133
LG:1086183.1:2000SEP08
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219
386


133
LG:1086183.1:2000SEP08
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76
302


133
LG:1086183.1:2000SEP08
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76
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133
LG:1086183.1:2000SEP08
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133
LG:1086183.1:2000SEP08
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218
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133
LG:1086183.1:2000SEP08
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1
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LG:1086183.1:2000SEP08
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1
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133
LG:1086183.1:2000SEP08
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474


133
LG:1086183.1:2000SEP08
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63
432


133
LG:1086183.1:2000SEP08
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49
668


133
LG:1086183.1:2000SEP08
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64
283


133
LG:1086183.1:2000SEP08
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76
442


133
LG:1086183.1:2000SEP08
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498
730


133
LG:1086183.1:2000SEP08
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687
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133
LG:1086183.1:2000SEP08
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695
959


133
LG:1086183.1:20003EP08
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735
1319


133
LG:1086183.1:2000SEP08
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753
874


133
LG:1086183.1:2000SEP08
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560


133
LG:1086183.1:2000SEP08
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470
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133
LG:1086183.1:2000SEP08 5621149R6
440
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133
LG:1086183.1:2000SEP08 2070125H1
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303


133
LG:1086183.1:2000SEP08 4739279H1
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133
LG:1086183.1:2000SEP08 5883746H1
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185


133
LG:1086183.1:2000SEP08 5883225H1
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LG:1086183.1:2000SEP08 6124139H1
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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1257
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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710
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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864
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134
LG:1090268.1:2000SEP08
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1208
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134
LG:1090268.1:2000SEP08
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1193
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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753
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134
LG:1090268.1:2000SEP08
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753
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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1195
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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753
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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762
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134
LG:1090268.1:2000SEP08
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802
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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806
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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LG:1090268.1:2000SEP08
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800
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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1190
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134
LG:1090268.1:2000SEP08
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981
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134
LG:1090268.1:2000SEP08
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1846
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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1251
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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2139
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134
LG:1090268.1:2000SEP08
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1826
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134
LG:1090268.1:2000SEP08
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1606
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134
LG:1090268.1:2000SEP08
3144079H1
1277
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134
LG:1090268.1:2000SEP08
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1930
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134
LG:1090268.1:2000SEP08
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650
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG: 1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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877
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134
LG:1090268.1:2000SEP08
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639
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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2209
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134
LG:1090268.1:2000SEP08
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1355
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134
LG:1090268.1:2000SEP08
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833
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134
LG:1090268.1:2000SEP08
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2030
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134
LG:1090268.1:2000SEP08
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1769
2031


134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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2028
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
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134
LG:1090268.1:2000SEP08
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134
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134
LG:1090268.1:2000SEP08
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909
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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900
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08 6753494H1
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134
LG:1090268.1:2000SEP08 6753494J1
581
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134
LG:1090268.1:2000SEP08 2930018H1
640
942


134
LG:1090268.1:2000SEP08
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674
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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877
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134
LG:1090268.1:2000SEP08
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980
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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1198
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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1277
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134
LG:1090268.1:2000SEP08
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1315
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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1405
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134
LG:1090268.1:20003EP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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1669
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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1790
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134
LG:1090268.1:2000SEP08
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1831
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134
LG:1090268.1:2000SEP08
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1832
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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1966
2178


134
LG:1090268.1:2000SEP08
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311
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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2041
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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2221
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:20003EP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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187
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134
LG:1090268.1:2000SEP08
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195
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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237
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08 7606141J1
1200
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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2258
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
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134
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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1669
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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134
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134
LG:1090268.1:2000SEP08
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134
LG:1090268.1:2000SEP08
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LG:1076866.1:2000SEP08
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LG:1076866.1:2000SEP08
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LG:1076866.1:2000SEP08
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LG:1076866.1:2000SEP08
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LG:1076866.1:2000SEP08
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LG:1076866.1:2000SEP08
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LG:1076866.1:2000SEP08
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146
LG:1076866.1:2000SEP08
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146
LG:1076866.1:2000SEP08
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LG:1076866.1:2000SEP08
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146
LG:1076866.1:2000SEP08
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146
LG:1076866.1:2000SEP08
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146
LG:1076866.1:2000SEP08
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146
LG:1076866.1:2000SEP08
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LG:1076866.1:2000SEP08
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303
560


146
LG:1076866.1:2000SEP08
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303
899


146
LG:1076866.1:2000SEP08
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332
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146
LG:1076866.1:2000SEP08
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457
919


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LG:1076866.1:2000SEP08
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556
944


146
LG:1076866.1:2000SEP08
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LG:1076866.1:2000SEP08
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797
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146
LG:1076866.1:2000SEP08
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1114
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146
LG:1076866.1:2000SEP08
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1114
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146
LG:1076866.1:2000SEP08
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1291
1870


146
LG:1076866.1:2000SEP08
1543396R61477
1987


146
LG:1076866.1:2000SEP08
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1574
1858


146
LG:1076866.1:2000SEP08
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1600
2178


146
LG:1076866.1:2000SEP08
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1610
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LG:1076866.1:2000SEP08
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519
944


146
LG:1076866.1:2000SEP08
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1796
2053


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LG:1076866.1:2000SEP08
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1477
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146
LG:1076866.1:2000SEP08
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146
LG:1076866.1:2000SEP08
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1600
2157


146
LG:1076866.1:2000SEP08
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1796
2039


146
LG:1076866.1:2000SEP08
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1755
2006


147
LG:969359.1:2000SEP08
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3
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147
LG:969359.1:2000SEP08
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3
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147
LG:969359.1:2000SEP08
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3
299


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LG:969359.1:2000SEP08
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3
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LG:969359.1:2000SEP08
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10
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LG:969359.1:2000SEP08
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169
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147
LG:969359.1:2000SEP08
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303
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147
LG:969359.1:2000SEP08
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599
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LG:969359.1:2000SEP08
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LG:969359.1:2000SEP08
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LG:969359.1:2000SEP08
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1 486


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1
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148
LG:366783.1:2000SEP08
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1080
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148
LG:366783.1:2000SEP08
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1069
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148
LG:366783.1:2000SEP08
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148
LG:366783.1:2000SEP08
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441
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148
LG:366783.1:2000SEP08
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441
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148
LG:366783.1:2000SEP08
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286
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148
LG:366783.1:2000SEP08
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1 472


149
LG:332176.3:2000SEP08
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203
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149
LG:332176.3:2000SEP08
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662
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LG:332176.3:2000SEP08
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149
LG:332176.3:2000SEP08
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856
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149
LG:332176.3:2000SEP08
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1
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149
LG:332176.3:2000SEP08
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32
318


149
LG:332176.3:2000SEP08
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100
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LG:332176.3:2000SEP08
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107
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LG:332176.3:2000SEP08
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133
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LG:332176.3:2000SEP08
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161
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150
LG:994938.1:2000SEP08
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1
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1
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LG:994938.1:2000SEP08
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LG:994938.1:2000SEP08
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LG:994938.1:2000SEP08
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LG:994938.1:2000SEP08
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LG:994938.1:2000SEP08
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LG:982800.1:2000SEP08
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2147
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LG:982800.1:2000SEP08
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LG:982800.1:2000SEP08
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LG:982800.1:2000SEP08
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LG:982800.1:2000SEP08
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2090
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2090
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151
LG:982800.1:2000SEP08
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2090
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LG:982800.1:2000SEP08
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LG:982800.1:2000SEP08
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LG:982800.1:2000SEP08
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LG:982800.1:2000SEP08
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LG:982800.1:2000SEP08
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LG:982800.1:2000SEP08
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LG:982800.1:2000SEP08
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LG:982800.1:2000SEP08
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LG:982800.1:2000SEP08
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LG:982800.1:2000SEP08
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LG:982800.1:2000SEP08
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LG:982800.1:2000SEP08 7335618H1
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LG:982800.1:2000SEP08
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LG:982800.1:2000SEP08
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LG:982800.1:2000SEP08
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LG:982800.1:2000SEP08
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LG:982800.1:2000SEP08
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LG:982800.1:2000SEP08
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151
LG:982800.1:2000SEP08
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1498
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151
LG:982800.1:2000SEP08
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LG:982800.1:2000SEP08
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1561
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151
LG:982800.1:2000SEP08
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151
LG:982800.1:2000SEP08
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151
LG:982800.1:2000SEP08
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2139


151
LG:982800.1:2000SEP08
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2028
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151
LG:982800.1:2000SEP08
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2028
2294


151
LG:982800.1:2000SEP08
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2051
2147


151
LG:982800.1:2000SEP08
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2162


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LG:982800.1:2000SEP08
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2165


151
LG:982800.1:2000SEP08
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2229


151
LG:982800.1:2000SEP08
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583
991


151
LG:982800.1:2000SEP08
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583
841


151
LG:982800.1:2000SEP08
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853
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151
LG:982800.1:2000SEP08
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853
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151
LG:982800.1:2000SEP08
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853
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LG:982800.1:2000SEP08
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1056
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151
LG:982800.1:2000SEP08
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1156
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151
LG:982800.1:2000SEP08
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1230
1497


151
LG:982800.1:2000SEP08
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356
465


151
LG:982800.1:2000SEP08
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399
886


151
LG:982800.1:2000SEP08
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399
860


151
LG:982800.1:2000SEP08
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407
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151
LG:982800.1:2000SEP08
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513
695


151
LG:982800.1:2000SEP08
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2157
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151
LG:982800.1:2000SEP08
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2161
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151
LG:982800.1:2000SEP08
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2175
2356


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LG:982800.1:2000SEP08
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2189
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151
LG:982800.1:2000SEP08
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2150
2362


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LG:982800.1:2000SEP08
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42
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LG:982800.1:2000SEP08
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307
888


151
LG:982800.1:2000SEP08
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1
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151
LG:982800.1:2000SEP08
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12
274


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LG:982800.1:2000SEP08
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2501
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LG:982800.1:2000SEP08
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2503
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151
LG:982800.1:2000SEP08
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151
LG:982800.1:2000SEP08
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2412
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152
LG:977850.7:2000SEP08
6832831H1
1
270


152
LG:977850.7:2000SEP08
6832952H1
2
270


153
LG:234748.2:2000SEP08
3810352H1
1966
2273


153
LG:234748.2:2000SEP08
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2081
2258


153
LG:234748.2:2000SEP08
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1956
2256


153
LG:234748.2:2000SEP08
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1794
2244


153
LG:234748.2:2000SEP08
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1953
2241


153
LG:234748.2:2000SEP08
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1629
2144


153
LG:234748.2:2000SEP08
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1611
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LG:234748.2:2000SEP08
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1782
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LG:234748.2:2000SEP08
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1823
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153
LG:234748.2:2000SEP08
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1756
2014


153
LG:234748.2:2000SEP08
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1758
1977


153
LG:234748.2:2000SEP08
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1546
1947


153
LG:234748.2:2000SEP08
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1651
1940


153
LG:234748.2:2000SEP08
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1025
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LG:234748.2:2000SEP08
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1022
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LG:234748.2:2000SEP08
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890
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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1177
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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1126
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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1030
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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520
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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617
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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648
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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550
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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604
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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2356
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LG:234748.2:2000SEP08
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2180
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LG:234748.2:2000SEP08
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2256
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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2346
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LG:234748.2:2000SEP08
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2043
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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2164
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LG:234748.2:2000SEP08
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2169
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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2178
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LG:234748.2:2000SEP08
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2163
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LG:234748.2:2000SEP08
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2285
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LG:234748.2:2000SEP08
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2211
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LG:234748.2:2000SEP08
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2146
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LG:234748.2:2000SEP08
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2216
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153
LG:234748.2:2000SEP08
93174864
2007
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153
LG:234748.2:2000SEP08
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1990
2308


153
LG:234748.2:2000SEP08
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1712
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153
LG:234748.2:2000SEP08
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24
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LG:234748.2:2000SEP08
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25
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LG:234748.2:20003EP08
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LG:234748.2:2000SEP08
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1
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LG:234748.2:2000SEP08
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114
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LG:234748.2:2000SEP08
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5
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LG:234748.2:2000SEP08
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98
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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1660
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LG:234748.2:2000SEP08
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1358
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LG:234748.2:2000SEP08
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1220
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LG:234748.2:2000SEP08
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1546
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LG:234748.2:2000SEP08
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1294
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LG:234748.2:2000SEP08
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1449
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LG:234748.2:2000SEP08
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1328
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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1344
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LG:234748.2:2000SEP08
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1294
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LG:234748.2:2000SEP08
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1008
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LG:234748.2:2000SEP08
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1228
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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254
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279
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280
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LG:234748.2:2000SEP08
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428
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LG:234748.2:2000SEP08
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94
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356
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LG:234748.2:2000SEP08
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1629
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1480
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LG:234748.2:2000SEP08
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1480
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LG:234748.2:2000SEP08
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LG:234748.2:2000SEP08
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LG:306284.1:2000SEP08
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167
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LG:306284.1:2000SEP08
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1
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LG:306284.1:2000SEP08
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1
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LG:306284.1:2000SEP08
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LI:333170.3:2000SEP08
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208
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LI:333170.3:2000SEP08
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245
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166
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247
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360
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246
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LI:333170.3:2000SEP08
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157
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LI:333170.3:2000SEP08
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156
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210
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LI:333170.3:2000SEP08
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181
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LI:333170.3:2000SEP08
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159
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LI:333170.3:2000SEP08
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LI:333170.3:2000SEP08
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480
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LI:333170.3:2000SEP08
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177
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155
LI:333170.3:2000SEP08
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233
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LI:333170.3:2000SEP08
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165
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LI:333170.3:2000SEP08
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304
617


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LI:333170.3:2000SEP08
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231
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LI:333170.3:2000SEP08
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310
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LI:286639.1:2000SEP08
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198
LI:286639.1:2000SEP08
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198
LI:286639.1:2000SEP08
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198
LI:286639.1:2000SEP08
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198
LI:286639.1:2000SEP08
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198
LI:286639.1:2000SEP08
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198
LI:286639.1:2000SEP08
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198
LI:286639.1:2000SEP08
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198
LI:286639.1:2000SEP08
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198
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198
LI:286639.1:2000SEP08
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198
LI:286639.1:2000SEP08
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198
LI:286639.1:2000SEP08
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198
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198
LI:286639.1:2000SEP08
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1444
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LI:286639.1:2000SEP08
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LI:286639.1:2000SEP08
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198
LI:286639.1:2000SEP08
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198
LI:286639.1:2000SEP08
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198
LI:286639.1:2000SEP08
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198
LI:286639.1:2000SEP08
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198
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198
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198
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198
LI:286639.1:2000SEP08
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2348


198
LI:286639.1:2000SEP08
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198
LI:286639.1:2000SEP08
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198
LI:286639.1:2000SEP08
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199
LI:288905.4:2000SEP08
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199
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199
LI:288905.4:2000SEP08
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810
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199
LI:288905.4:2000SEP08
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199
LI:288905.4:2000SEP08
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2331


199
LI:288905.4:2000SEP08
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199
LI:288905.4:2000SEP08
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199
LI:288905.4:2000SEP08
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199
LI:288905.4:2000SEP08
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199
LI:288905.4:2000SEP08
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1771
2336


199
LI:288905.4:2000SEP08
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740
1 150


199
LI:288905.4:2000SEP08
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609
1146


199
LI:288905.4:2000SEP08
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1003
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199
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199
LI:288905.4:2000SEP08
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1132
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199
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199
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199
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199
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199
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199
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1719
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199
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199
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199
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199
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199
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199
LI:288905.4:2000SEP08
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201
822


199
LI:288905.4:2000SEP08
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190
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199
LI:288905.4:2000SEP08
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199
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199
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199
LI:288905.4:2000SEP08
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925
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199
LI:288905.4:2000SEP08
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199
LI:288905.4:2000SEP08
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1351
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199
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199
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199
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199
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199
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199
LI:288905.4:2000SEP08
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928
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199
LI:288905.4:2000SEP08
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200
LI:332161.1:2000SEP08
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200
LI:332161.1:2000SEP08
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200
LI:332161.1:2000SEP08
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1127
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200
LI:332161.1:2000SEP08
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1379
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200
LI:332161.1:2000SEP08
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1435
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200
LI:332161.1:2000SEP08
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2587
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200
LI:332161.1:2000SEP08
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2497
2732


200
LI:332161.1:2000SEP08
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200
LI:332161.1:2000SEP08
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2445
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200
LI:332161.1:2000SEP08
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2449
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200
LI:332161.1:20003EP08
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200
LI:332161.1:2000SEP08
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200
LI:332161.1:2000SEP08
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200
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200
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200
LI:332161.1:2000SEP08
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200
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200
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200
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200
LI:332161.1:2000SEP08
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200
LI:332161.1:2000SEP08
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2416
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200
LI:332161.1:2000SEP08
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200
LI:332161.1:2000SEP08
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3047


200
LI:332161.1:2000SEP08
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1753
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200
LI:332161.1:2000SEP08
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1794
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200
LI:332161.1:2000SEP08
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200
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200
LI:332161.1:2000SEP08
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200
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2525
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200
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2530
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200
LI:332161.1:2000SEP08
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2517
3024


200
LI:332161.1:2000SEP08
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1997
2237


200
LI:332161.1:2000SEP08
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2693
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200
LI:332161.1:2000SEP08
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2513
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200
LI:332161.1:2000SEP08
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1973
2289


200
LI:332161.1:2000SEP08
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2714
3054


200
LI:332161.1:2000SEP08
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200
LI:332161.1:2000SEP08
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200
LI:332161.1:2000SEP08
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2758
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200
LI:332161.1:2000SEP08
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2758
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200
LI:332161.1:2000SEP08
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1855
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200
LI:332161.1:2000SEP08
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1948
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200
LI:332161.1:2000SEP08
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200
LI:332161.1:2000SEP08
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200
LI:332161.1:2000SEP08
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1
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200
LI:332161.1:2000SEP08
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200
LI:332161.1:2000SEP08
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1656
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200
LI:332161.1:2000SEP08
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200
LI:332161.1:2000SEP08
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200
LI:332161.1:2000SEP08
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200
LI:332161.1:2000SEP08
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200
LI:332161.1:2000SEP08
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1619
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200
LI:332161.1:2000SEP08
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1656
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200
LI:332161.1:2000SEP08
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200
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200
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200
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200
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200
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200
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129
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200
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200
LI:332161.1:2000SEP08
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200
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200
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200
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200
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200
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200
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200
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200
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200
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200
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200
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200
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200
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200
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200
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200
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200
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200
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200
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200
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200
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200
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200
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200
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200
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200
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2320
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200
LI:332161.1:2000SEP08
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200
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200
LI:332161.1:2000SEP08
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200
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200
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200
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201
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201
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201
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342
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201
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201
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201
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201
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201
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201
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386
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201
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417
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201
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201
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201
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201
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201
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201
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202
LI:229932.4:2000SEP08
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202
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202
LI:229932.4:2000SEP08
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202
LI:229932.4:2000SEP08
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1
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202
LI:229932.4:2000SEP08
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11
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202
LI:229932.4:2000SEP08
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202
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202
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202
LI:229932.4:2000SEP08
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202
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202
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202
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202
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202
LI:229932.4:2000SEP08
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202
LI:229932.4:2000SEP08
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218
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218
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657
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230
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231
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1803
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231
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2552
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231
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2539
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512
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231
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231
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304
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231
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1132
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2085
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231
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2088
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1835
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231
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1854
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231
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2017
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231
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231
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231
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231
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976
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231
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231
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231
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1786
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231
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231
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231
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231
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231
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1552
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231
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1589
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231
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1639
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231
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1648
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231
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1674
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231
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1992
2359


231
LI:2050313.1:2000SEP08
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1992
2629


231
LI:2050313.1:2000SEP08
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1994
2665


231
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231
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2435
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231
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1946
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231
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1946
2241


231
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1958
2269


231
LI:2050313.1:2000SEP08
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1958
2280


231
LI:2050313.1:2000SEP08
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2979
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231
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231
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231
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231
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231
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231
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2473
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231
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2481
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231
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2454
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231
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2458
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231
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231
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231
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2435
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231
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292
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231
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231
LI:2050313.1:2000SEP08
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231
LI:2050313.1:2000SEP08
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1982
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231
LI:2050313.1:2000SEP08
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1983
2430


231
LI:2050313.1:2000SEP08
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1986
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231
LI:2050313.1:2000SEP08
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2614
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231
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1132
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231
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231
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231
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231
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231
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1122
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231
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231
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231
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231
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231
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231
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2017
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231
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231
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231
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1923
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231
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1931
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231
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1935
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231
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1937
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231
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1976
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231
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1986
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1968
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1971
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231
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1985
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231
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2001
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231
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1982
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231
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231
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231
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231
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231
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231
LI:2050313.1:2000SEP08
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1980
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231
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1962
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231
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231
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2346
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232
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236
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2266


250
LI:1144409.1:2000SEP08
955100T2
2090
2570


250
LI:1144409.1:2000SEP08
955100R1
2090
2453


250
LI:1144409.1:2000SEP08
955100H1
2090
2358


250
LI:1144409.1:2000SEP08
3814175T6
2095
2570


251
LI:246290.10:2000SEP08
7160791H1
485
997


251
LI:246290.10:2000SEP08
1320454H1
499
734


251
LI:246290.10:2000SEP08
7644139J1
512
1059


251
LI:246290.10:2000SEP08
6723259H1
516
916


251
LI:246290.10:2000SEP08
747973R6
330
859


251
LI:246290.10:2000SEP08
747973H1
330
572


251
LI:246290.10:2000SEP08
7170570H1
383
910


251
LI:246290.10:2000SEP08
5080008H1
88
328


251
LI:246290.10:2000SEP08
5957953H1
89
545


251
LI:246290.10:2000SEP08
6937991H1
99
200


251
LI:246290.10:2000SEP08
7168155H1
137
243


251
LI:246290.10:2000SEP08
4831526F8
229
767


251
LI:246290.10:2000SEP08
4831526H1
230
359


251
LI:246290.10:2000SEP08
4831526F9
229
744


251
LI:246290.10:2000SEP08
7387420H1
285
504


251
LI:246290.10:2000SEP08
5761576H1
540
807


251
LI:246290.10:2000SEP08
4930979H1
612
891


251
LI:246290.10:2000SEP08
806868H1
728
958


251
LI:246290.10:2000SEP08
6866060H1
68
403


251
LI:246290.10:2000SEP08
3506257H1
73
350


251
LI:246290.10:2000SEP08
3550395H1
1
288


251
LI:246290.10:2000SEP08
7988114H1
2
511


251
LI:246290.10:2000SEP08
3316757H1
18
304


251
LI:246290.10:2000SEP08
8122994H1
19
612


251
LI:246290.10:2000SEP08
5457648H1
23
233


251
LI:246290.10:2000SEP08
3508411H1
23
303


251
LI:246290.10:2000SEP08
3577541H1
23
287


251
LI:246290.10:2000SEP08
5460535H1
23
271


251
LI:246290.10:2000SEP08
7002420H1
39
596


251
LI:246290.10:2000SEP08
4328953H1
42
304


251
LI:246290.10:2000SEP08
3973335H1
57
325


251
LI:246290.10:2000SEP08
7470753H1
67
633


251
LI:246290.10:2000SEP08
2966230H1
1
297


251
LI:246290.10:2000SEP08
2966230F6
1
377


252
LI:280034.1:2000SEP08
8045415H1
1
646


252
LI:280034.1:2000SEP08
8045415J1
482
1096


252
LI:280034.1:2000SEP08
681866T6
584
802


252
LI:280034.1:2000SEP08
681866H1
584
845


252
LI:280034.1:2000SEP08
681866R6
584
841


252
LI:280034.1:2000SEP08
4936924H1
781
1020










[0305]

7







TABLE 6








SEQ ID NO:
Template ID
Tissue Distribution

















1
LG:150318.1:2000SEP08
Nervous System - 100%


2
LG:022529.1:2000SEP08
Musculoskeletal System - 25%, Unclassified/Mixed - 22%, Cardiovascular




System - 14%


3
LG:352559.1:2000SEP08
Unclassified/Mixed - 67%, Digestive System - 33%


4
LG:175223.1:2000SEP08
Embryonic Structures - 82%, Nervous System - 18%


5
LG:476989.1:2000SEP08
Exocrine Glands - 62%, Urinary Tract - 31%


6
LG:253268.7:2000SEP08
Germ Cells - 56%, Nervous System - 23%


7
LG:401322.1:2000SEP08
Sense Organs - 50%, Liver - 17%, Skin - 13%


8
LG:1328436.1:2000SEP08
Respiratory System - 38%, Endocrine System - 35%, Connective Tissue -




27%


9
LG:475404.1:2000SEP08
Skin - 81%


10
LG:1384132.1:2000SEP08
Respiratory System - 50%, Digestive System - 33%, Nervous System - 17%


11
LG:410804.18:2000SEP08
Nervous System - 100%


12
LG:1082306.1:2000SEP08
Cardiovascular System - 28%, Digestive System - 21%, Exocrine Glands -




14%, Endocrine System - 14%


13
LG:233814.4:2000SEP08
Endocrine System - 36%, Pancreas - 36%, Exocrine Glands - 16%


14
LG:977478.5:2000SEP08
Cardiovascular System - 34%, Musculoskeletal System - 19%, Female




Genitalia - 16%


15
LG:025931.1:2000SEP08
Female Genitalia - 29%, Urinary Tract - 24%, Endocrine System - 24%


16
LG:885368.1:2000SEP08
Nervous System - 67%, Female Genitalia - 33%


17
LG:1054900.1:2000SEP08
Digestive System - 50%, Female Genitalia - 25%, Male Genitalia - 25%


18
LG:995186.2:2000SEP08
Digestive System - 67%, Nervous System - 33%


19
LG:435048.23:2000SEP08
Urinary Tract - 80%, Nervous System - 20%


20
LG:954859.1:2000SEP08
Embryonic Structures - 56%, Hemic and Immune System - 19%, Female




Genitalia - 13%, Nervous System - 13%


21
LG:364370.1:2000SEP08
Liver - 90%, Male Genitalia - 10%


22
LG:1098789.1:2000SEP08
Urinary Tract - 100%


23
LG:201540.2:2000SEP08
Unclassified/Mixed - 15%, Female Genitalia - 13%, Connective Tissue -




13%, Male Genitalia - 13%


24
LG:1077357.1:2000SEP08
Nervous System - 43%, Male Genitalia - 29%, Female Genitalia - 29%


25
LG:1048846.4:2000SEP08
Female Genitalia - 25%, Digestive System - 25%, Male Genitalia - 25%


26
LG:336685.1:2000SEP08
Hemic and Immune System - 35%, Urinary Tract - 24%, Male Genitalia -




24%


27
LG:1076253.1:2000SEP08
Liver - 50%, Urinary Tract - 11%, Endocrine System - 11%


28
LG:1400601.2:2000SEP08
Skin - 100%


29
LG:1079092.3:2000SEP08
Musculoskeletal System - 100%


30
LG:1086064.1:2000SEP08
Skin - 69%


31
LG:1400608.1:2000SEP08
Female Genitalia - 26%, Urinary Tract - 21%, Respiratory System - 16%


32
LG:399275.5:2000SEP08
Respiratory System - 50%, Male Genitalia - 33%, Hemic and Immune




System - 17%


33
LG:293943.1:2000SEP08
Exocrine Glands - 50%, Digestive System - 25%, Hemic and Immune




System - 13%, Nervous System - 13%


34
LG:345884.1:2000SEP08
Respiratory System - 63%, Hemic and Immune System - 38%


35
LG:400967.1:2000SEP08
Embryonic Structures - 36%, Urinary Tract - 28%, Cardiovascular System -




16%


36
LG:024556.6:2000SEP08
Nervous System - 89%, Male Genitalia - 11%


37
LG:081189.3:2000SEP08
Germ Cells - 88%


38
LG:018258.1:2000SEP08
Digestive System - 44%, Endocrine System - 44%, Hemic and Immune




System - 11%


39
LG:450399.3:2000SEP08
Nervous System - 100%


40
LG:451122.1:2000SEP08
Nervous System - 100%


41
LG:451682.1:2000SEP08
Nervous System - 100%


42
LG:238631.4:2000SEP08
Liver - 17%, Endocrine System - 14%, Respiratory System - 11%, Male




Genitalia - 11%


43
LG:236654.1:2000SEP08
Unclassified/Mixed - 38%, Respiratory System - 15%


44
LG:332655.1:2000SEP08
Pancreas - 26%, Digestive System - 17%, Female Genitalia - 13%


45
LG:217396.2:2000SEP08
Skin - 24%, Embryonic Structures - 15%, Pancreas - 15%


46
LG:090574.1:2000SEP08
Respiratory System - 100%


47
LG:202943.1:2000SEP08
Embryonic Structures - 44%, Female Genitalia - 19%, Liver - 14%


48
LG:236928.1:2000SEP08
Unclassified/Mixed - 15%, Hemic and Immune System - 14%, Nervous




System - 12%


49
LG:215169.2:2000SEP08
Endocrine System - 22%, Unclassified/Mixed - 20%, Nervous System - 20%


50
LG:410726.1:2000SEP08
Embryonic Structures - 38%, Pancreas - 24%, Endocrine System - 18%


51
LG:234372.2:2000SEP08
Stomatognathic System - 17%, Germ Cells - 12%, Musculoskeletal System -




11%


52
LG:022629.1:2000SEP08
Unclassified/Mixed - 36%, Germ Cells - 28%


53
LG:068682.1:2000SEP08
Unclassified/Mixed - 61%, Male Genitalia - 20%


54
LG:222335.1:2000SEP08
Musculoskeletal System - 27%, Exocrine Glands - 17%, Male Genitalia -




13%


55
LG:331342.1:2000SEP08
Male Genitalia - 35%, Digestive System - 22%, Endocrine System - 20%


56
LG:021770.1:2000SEP08
Pancreas - 18%, Exocrine Glands - 14%, Nervous System - 12%, Urinary




Tract - 12%, Male Genitalia - 12%


57
LG:181607.9:2000SEP08
Musculoskeletal System - 25%, Cardiovascular System - 22%, Embryonic




Structures - 18%


58
LG:1042768.1:2000SEP08
Liver - 100%


59
LG:282729.1:2000SEP08
Skin - 74%, Unclassified/Mixed - 21%


60
LG:998305.3:2000SEP08
Urinary Tract - 50%, Cardiovascular System - 29%, Nervous System - 21%


61
LG:1135213.1:2000SEP08
Embryonic Structures - 26%, Cardiovascular System - 20%, Digestive




System - 11%, Unclassified/Mixed - 11%


62
LG:267762.1:2000SEP08
Cardiovascular System - 16%, Urinary Tract - 14%, Connective Tissue -




14%


63
LG:120744.1:2000SEP08
Skin - 35%, Embryonic Structures - 23%, Digestive System - 20%


64
LG:403409.1:2000SEP08
Stomatognathic System - 45%, Respiratory System - 12%


65
LG:226874.3:2000SEP08
Respiratory System - 38%, Male Genitalia - 35%, Female Genitalia - 19%


66
LG:1045521.4:2000SEP08
Germ Cells - 16%


67
LG:275876.1:2000SEP08
Unclassified/Mixed - 53%, Endocrine System - 27%, Nervous System - 20%


68
LG:475127.7:2000SEP08
Hemic and Immune System - 75%, Nervous System - 25%


69
LG:157263.1:2000SEP08
Embryonic Structures - 39%, Urinary Tract - 30%


70
LG:247382.7:2000SEP08
Urinary Tract - 19%, Hemic and Immune System - 13%, Embryonic




Structures - 13%, Endocrine System - 13%


71
LG:197367.5:2000SEP08
Endocrine System - 100%


72
LG:218090.5:2000SEP08
Unclassified/Mixed - 42%, Urinary Tract - 21%, Exocrine Glands - 21%


73
LG:216612.4:2000SEP08
Nervous System - 45%, Digestive System - 30%, Endocrine System - 20%


74
LG:197614.1:2000SEP08
Germ Cells - 17%, Unclassified/Mixed - 16%


75
LG:378428.1:2000SEP08
Liver - 30%, Endocrine System - 15%, Embryonic Structures - 15%


76
LG:286639.1:2000SEP08
Germ Cells - 72%


77
LG:389870.1:2000SEP08
Liver - 41%, Nervous System - 23%, Cardiovascular System - 18%,




Endocrine System - 18%


78
LG:1387485.6:2000SEP08
Female Genitalia - 16%, Digestive System - 14%, Urinary Tract - 13%


79
LG:230151.1:2000SEP08
Exocrine Glands - 16%, Urinary Tract - 14%, Liver - 12%, Pancreas - 12%


80
LG:215158.5:2000SEP08
Liver - 13%, Nervous System - 12%, Unclassified/Mixed - 11%


81
LG:235840.1:2000SEP08
Connective Tissue - 13%, Nervous System - 12%, Hemic and Immune




System - 11%, Liver - 11%


82
LG:350272.1:2000SEP08
Germ Cells - 17%, Musculoskeletal System - 15%


83
LG:232190.1:2000SEP08
Liver - 24%, Unclassified/Mixed - 23%, Skin - 19%


84
LG:1068127.1:2000SEP08
Hemic and Immune System - 43%, Male Genitalia - 29%, Nervous System -




29%


85
LG:408751.3:2000SEP08
Nervous System - 43%, Sense Organs - 31%


86
LG:1078933.1:2000SEP08
Liver - 23%, Unclassified/Mixed - 20%, Nervous System - 13%


87
LG:958731.1:2000SEP08
Nervous System - 100%


88
LG:024125.5:2000SEP08
Connective Tissue - 17%, Embryonic Structures - 16%


89
LG:373637.3:2000SEP08
Unclassified/Mixed - 73%, Male Genitalia - 23%


90
LG:1053229.1:2000SEP08
Cardiovascular System - 50%, Embryonic Structures - 41%


91
LG:248364.1:2000SEP08
Sense Organs - 48%, Female Genitalia - 17%


92
LG:477130.1:2000SEP08
Nervous System - 100%


93
LG:113786.17:2000SEP08
Hemic and Immune System - 100%


94
LG:347635.1:2000SEP08
Musculoskeletal System - 45%, Female Genitalia - 17%, Urinary Tract -




14%


95
LG:242966.4:2000SEP08
Germ Cells - 23%, Stomatognathic System - 23%


96
LG:217814.1:2000SEP08
Skin - 25%, Liver - 16%, Unclassified/Mixed - 15%


97
LG:476452.1:2000SEP08
Nervous System - 100%


98
LG:1100657.1:2000SEP08
Liver - 100%


99
LG:1132418.2:2000SEP08
Cardiovascular System - 100%


100
LG:1098570.1:2000SEP08
Liver - 100%


101
LG:1097987.1:2000SEP08
Embryonic Structures - 41%, Musculoskeletal System - 27%, Female




Genitalia - 23%


102
LG:337818.2:2000SEP08
Digestive System - 35%, Liver - 13%, Female Genitalia - 10%


103
LG:1040582.1:2000SEP08
Liver - 38%, Pancreas - 38%, Cardiovascular System - 17%


104
LG:1099122.1:2000SEP08
Liver - 96%


105
LG:1327449.1:2000SEP08
Endocrine System - 40%, Respiratory System - 30%, Digestive System -




20%


106
LG:227933.5:2000SEP08
Male Genitalia - 33%, Nervous System - 21%, Female Genitalia - 15%


107
LG:1043709.2:2000SEP08
Liver - 100%


108
LG:1099871.1:2000SEP08
Liver - 90%, Nervous System - 10%


109
LG:1399139.4:2000SEP08
Unclassified/Mixed - 30%, Male Genitalia - 26%, Musculoskeletal System -




22%


110
LG:236386.1:2000SEP08
Skin - 16%, Connective Tissue - 13%, Pancreas - 10%


111
LG:1015157.1:2000SEP08
Liver - 100%


112
LG:1065433.1:2000SEP08
Female Genitalia - 50%, Endocrine System - 40%, Nervous System - 10%


113
LG:236992.4:2000SEP08
Connective Tissue - 64%, Urinary Tract - 12%, Cardiovascular System -




12%


114
LG:1071124.1:2000SEP08
Unclassified/Mixed - 22%, Cardiovascular System - 22%, Urinary Tract -




19%


115
LG:206425.2:2000SEP08
Sense Organs - 39%, Female Genitalia - 10%


116
LG:885747.2:2000SEP08
Female Genitalia - 100%


117
LG:1140501.1:2000SEP08
Sense Organs - 20%, Nervous System - 15%


118
LG:001239.1:2000SEP08
Hemic and Immune System - 35%, Liver - 17%, Male Genitalia - 13%


119
LG:018980.1:2000SEP08
Unclassified/Mixed - 52%, Urinary Tract - 12%, Nervous System - 12%


120
LG:1083120.3:2000SEP08
Digestive System - 50%, Hemic and Immune System - 25%, Nervous




System - 25%


121
LG:233258.3:2000SEP08
Germ Cells - 25%, Female Genitalia - 12%


122
LG:999062.1:2000SEP08
Nervous System - 100%


123
LG:887776.1:2000SEP08
Cardiovascular System - 35%, Skin - 33%, Hemic and Immune System -




14%


124
LG:1400301.2:2000SEP08
Exocrine Glands - 50%, Connective Tissue - 44%


125
LG:1329362.1:2000SEP08
Unclassified/Mixed - 44%, Urinary Tract - 22%, Exocrine Glands - 22%


126
LG:1096498.1:2000SEP08
Liver - 100%


127
LG:1096337.1:2000SEP08
Urinary Tract - 40%, Exocrine Glands - 40%, Nervous System - 20%


128
LG:1400579.1:2000SEP08
Liver - 53%, Musculoskeletal System - 25%


129
LG:1080091.1:2000SEP08
Connective Tissue - 21%, Musculoskeletal System - 18%, Female




Genitalia - 15%


130
LG:1082203.1:2000SEP08
Embryonic Structures - 23%, Endocrine System - 11%, Male Genitalia -




11%


131
LG:1084051.1:2000SEP08
Germ Cells - 33%, Pancreas - 11%, Male Genitalia - 11%


132
LG:1082393.1:2000SEP08
Male Genitalia - 20%, Urinary Tract - 13%, Unclassified/Mixed - 13%


133
LG:1086183.1:2000SEP08
Liver - 25%, Skin - 20%, Hemic and Immune System - 14%


134
LG:1090268.1:2000SEP08
Sense Organs - 40%, Unclassified/Mixed - 17%


135
LG:1400597.5:2000SEP08
Unclassified/Mixed - 53%, Connective Tissue - 47%


136
LG:1080307.2:2000SEP08
Digestive System - 100%


137
LG:1400603.2:2000SEP08
Germ Cells - 40%, Nervous System - 18%, Unclassified/Mixed - 12%


138
LG:1052984.1:2000SEP08
Skin - 31%, Musculoskeletal System - 15%, Endocrine System - 10%,




Pancreas - 10%


139
LG:1091259.1:2000SEP08
Connective Tissue - 66%, Respiratory System - 25%


140
LG:1082263.2:2000SEP08
Embryonic Structures - 32%, Endocrine System - 15%, Nervous System -




10%


141
LG:1048604.2:2000SEP08
Exocrine Glands - 50%, Embryonic Structures - 38%


142
LG:1085254.3:2000SEP08
Embryonic Structures - 61%, Respiratory System - 32%


143
LG:1400606.2:2000SEP08
Embryonic Structures - 34%, Unclassified/Mixed - 14%, Nervous System -




13%, Connective Tissue - 13%


144
LG:1090358.2:2000SEP08
Urinary Tract - 36%, Male Genitalia - 23%, Hemic and Immune System -




15%, Musculoskeletal System - 15%


145
LG:1079064.2:2000SEP08
Nervous System - 21%, Female Genitalia - 16%, Liver - 12%


146
LG:1076866.1:2000SEP08
Germ Cells - 28%, Embryonic Structures - 20%, Cardiovascular System -




12%


147
LG:969359.1:2000SEP08
Liver - 79%, Pancreas - 19%


148
LG:366783.1:2000SEP08
Sense Organs - 95%


149
LG:332176.3:2000SEP08
Pancreas - 28%, Connective Tissue - 22%, Urinary Tract - 22%


150
LG:994938.1:2000SEP08
Exocrine Glands - 50%, Respiratory System - 21%, Urinary Tract - 17%


151
LG:982800.1:2000SEP08
Urinary Tract - 22%, Skin - 21%, Germ Cells - 13%


152
LG:977850.7:2000SEP08
Exocrine Glands - 100%


153
LG:234748.2:2000SEP08
Sense Organs - 27%, Urinary Tract - 15%, Unclassified/Mixed - 11%


154
LG:306284.1:2000SEP08
Nervous System - 60%, Male Genitalia - 40%


155
LI:333170.3:2000SEP08
Germ Cells - 82%, Unclassified/Mixed - 13%


156
LI:336685.2:2000SEP08
Hemic and Immune System - 35%, Male Genitalia - 25%, Urinary Tract -




20%


157
LI:279013.5:2000SEP08
Female Genitalia - 100%


158
LI:1037075.1:2000SEP08
Musculoskeletal System - 94%


159
LI:1073403.1:2000SEP08
Liver - 100%


160
LI:1075296.1:2000SEP08
Liver - 100%


161
LI:1085501.1:2000SEP08
Connective Tissue - 100%


162
LI:1086181.1:2000SEP08
Liver - 100%


163
LI:1164493.1:2000SEP08
Urinary Tract - 52%, Female Genitalia - 20%, Digestive System - 12%, Male




Genitalia - 12%


164
LI:1175097.1:2000SEP08
Unclassified/Mixed - 57%, Digestive System - 21%, Nervous System - 21%


165
LI:1092948.1:2000SEP08
Embryonic Structures - 26%, Connective Tissue - 19%, Musculoskeletal




System - 17%


166
LI:380378.2:2000SEP08
Nervous System - 100%


167
LI:1029674.1:2000SEP08
Digestive System - 42%, Nervous System - 36%, Unclassified/Mixed - 22%


169
LI:1186208.1:2000SEP08
Stomatognathic System - 51%, Sense Organs - 38%


170
LI:1170753.1:2000SEP08
Endocrine System - 95%


171
LI:1180908.1:2000SEP08
Skin - 21%, Embryonic Structures - 14%, Male Genitalia - 13%


172
LI:1182900.2:2000SEP08
Digestive System - 47%, Pancreas - 34%, Respiratory System - 19%


173
LI:1169548.2:2000SEP08
Nervous System - 100%


174
LI:1039974.1:2000SEP08
Female Genitalia - 31%, Urinary Tract - 29%, Nervous System - 16%


175
LI:1175765.2:2000SEP08
Nervous System - 100%


176
LI:313948.1:2000SEP08
Unclassified/Mixed - 31%, Endocrine System - 23%, Cardiovascular




System - 19%


177
LI:335923.2:2000SEP08
Germ Cells - 74%, Male Genitalia - 26%


178
LI:345884.1:2000SEP08
Respiratory System - 75%, Hemic and Immune System - 25%


179
LI:417127.1:2000SEP08
Connective Tissue - 100%


180
LI:451710.1:2000SEP08
Connective Tissue - 90%, Nervous System - 10%


181
LI:406882.2:2000SEP08
Sense Organs - 34%, Unclassified/Mixed - 15%, Nervous System - 15%


182
LI:728223.1:2000SEP08
Nervous System - 100%


183
LI:289783.19:2000SEP08
Digestive System - 38%, Unclassified/Mixed - 15%, Respiratory System -




12%


184
LI:235255.8:2000SEP08
Exocrine Glands - 23%, Connective Tissue - 12%, Female Genitalia - 11%


185
LI:237693.5:2000SEP08
Urinary Tract - 32%, Hemic and Immune System - 25%, Endocrine System -




21%


186
LI:433670.3:2000SEP08
Nervous System - 50%, Male Genitalia - 25%, Digestive System - 25%


187
LI:202943.4:2000SEP08
Embryonic Structures - 42%, Liver - 19%, Unclassified/Mixed - 16%


188
LI:068682.1:2000SEP08
Unclassified/Mixed - 47%, Digestive System - 21%, Male Genitalia - 19%


189
LI:203301.3:2000SEP08
Germ Cells - 19%, Male Genitalia - 14%, Respiratory System - 12%


190
LI:020726.3:2000SEP08
Sense Organs - 79%


191
LI:027209.1:2000SEP08
Musculoskeletal System - 53%, Female Genitalia - 27%, Exocrine Glands -




17%


192
LI:108819.1:2000SEP08
Urinary Tract - 45%, Digestive System - 28%, Skin - 15%


193
LI:021759.1:2000SEP08
Hemic and Immune System - 40%, Nervous System - 22%, Liver - 11%


194
LI:1165967.1:2000SEP08
Liver - 50%, Stomatognathic System - 50%


195
LI:1166315.1:2000SEP08
Cardiovascular System - 33%, Urinary Tract - 27%, Female Genitalia -




20%, Hemic and Immune System - 20%


196
LI:204626.1:2000SEP08
Digestive System - 58%, Nervous System - 15%, Exocrine Glands - 13%


197
LI:801140.1:2000SEP08
Embryonic Structures - 50%, Cardiovascular System - 38%


198
LI:286639.1:2000SEP08
Germ Cells - 64%


199
LI:288905.4:2000SEP08
Unclassified/Mixed - 76%, Nervous System - 24%


200
LI:332161.1:2000SEP08
Cardiovascular System - 47%, Nervous System - 14%, Connective Tissue -




10%


201
LI:184867.1:2000SEP08
Unclassified/Mixed - 33%, Embryonic Structures - 24%, Male Genitalia -




16%


202
LI:229932.4:2000SEP08
Musculoskeletal System - 40%, Cardiovascular System - 21%


203
LI:1189932.1:2000SEP08
Embryonic Structures - 37%, Germ Cells - 18%, Sense Organs - 13%


204
LI:1076689.1:2000SEP08
Liver - 99%


205
LI:415181.2:2000SEP08
Nervous System - 100%


206
LI:296358.1:2000SEP08
Hemic and Immune System - 83%


207
LI:205186.3:2000SEP08
Cardiovascular System - 59%, Male Genitalia - 20%, Unclassified/Mixed -




16%


208
LI:220537.2:2000SEP08
Stomatognathic System - 52%, Male Genitalia - 32%


209
LI:248364.2:2000SEP08
Cardiovascular System - 30%, Female Genitalia - 23%, Sense Organs -




22%


210
LI:2048338.1:2000SEP08
Connective Tissue - 90%, Nervous System - 10%


211
LI:1185203.8:2000SEP08
Nervous System - 75%, Female Genitalia - 25%


212
LI:021770.3:2000SEP08
Pancreas - 77%


213
LI:1185841.1:2000SEP08
Hemic and Immune System - 30%, Respiratory System - 26%


214
LI:1181710.1:2000SEP08
Male Genitalia - 38%, Nervous System - 38%, Hemic and Immune System -




25%


215
LI:2048959.1:2000SEP08
Musculoskeletal System - 73%, Endocrine System - 27%


216
LI:798494.1:2000SEP08
Germ Cells - 88%


217
LI:2049223.1:2000SEP08
Male Genitalia - 60%, Hemic and Immune System - 40%


218
LI:1177833.1:2000SEP08
Liver - 55%, Embryonic Structures - 10%


219
LI:2049267.1:2000SEP08
Cardiovascular System - 36%, Urinary Tract - 29%, Digestive System - 21%


220
LI:1165939.1:2000SEP08
Sense Organs - 62%, Endocrine System - 20%


221
LI:1170958.1:2000SEP08
Exocrine Glands - 53%, Cardiovascular System - 26%, Male Genitalia -




16%


222
LI:1089827.1:2000SEP08
Endocrine System - 16%, Male Genitalia - 13%, Musculoskeletal System -




12%


223
LI:792112.1:2000SEP08
Liver - 83%


224
LI:282219.2:2000SEP08
Embryonic Structures - 55%, Exocrine Glands - 23%, Male Genitalia - 14%


225
LI:1088010.2:2000SEP08
Exocrine Glands - 31%, Musculoskeletal System - 23%, Respiratory System -




13%


226
LI:1165276.1:2000SEP08
Nervous System - 18%, Male Genitalia - 16%, Pancreas - 16%


227
LI:1169524.2:2000SEP08
Endocrine System - 41%, Urinary Tract - 16%, Musculoskeletal System -




14%, Male Genitalia - 14%


228
LI:1180255.1:2000SEP08
Female Genitalia - 66%, Liver - 11%, Embryonic Structures - 11%


229
LI:1091903.1:2000SEP08
Germ Cells - 93%


230
LI:1169219.1:2000SEP08
Sense Organs - 34%, Skin - 22%


231
LI:2050313,1:2000SEP08
Skin - 15%, Respiratory System - 14%, Male Genitalia - 14%


232
LI:209351.3:2000SEP08
Cardiovascular System - 41%


233
LI:119900.1:2000SEP08
Stomatognathic System - 77%


234
LI:2052274.1:2000SEP08
Urinary Tract - 31%, Female Genitalia - 19%, Liver - 12%


235
LI:1075502.1:2000SEP08
Liver - 100%


236
LI:813697.1:2000SEP08
Endocrine System - 36%, Unclassified/Mixed - 25%, Exocrine Glands - 15%


237
LI:814261.1:2000SEP08
Exocrine Glands - 50%, Respiratory System - 20%, Urinary Tract - 13%


238
LI:775334.1:2000SEP08
Cardiovascular System - 26%, Embryonic Structures - 23%,




Unclassified/Mixed - 15%


239
LI:1180325.1:2000SEP08
Skin - 38%, Pancreas - 23%, Female Genitalia - 23%


240
LI:1183147.3:2000SEP08
Female Genitalia - 42%, Respiratory System - 17%, Nervous System - 13%


241
LI:1175373.3:2000SEP08
Nervous System - 50%, Male Genitalia - 25%, Digestive System - 25%


242
LI:813757.1:2000SEP08
Female Genitalia - 50%, Nervous System - 50%


243
LI:1182979.2:2000SEP08
Respiratory System - 67%, Pancreas - 19%


244
LI:1177823.2:2000SEP08
Embryonic Structures - 48%, Cardiovascular System - 20%, Exocrine




Glands - 20%


245
LI:1174279.1:2000SEP08
Endocrine System - 36%, Nervous System - 19%, Liver - 18%


246
LI:1178411.1:2000SEP08
Nervous System - 21%, Liver- 18%, Exocrine Glands - 15%


247
LI:1182739.1:2000SEP08
Unclassified/Mixed - 34%, Skin - 18%, Nervous System - 12%


248
LI:234937.4:2000SEP08
Endocrine System - 33%, Nervous System - 24%, Digestive System - 21%


249
LI:1170660.1:2000SEP08
Musculoskeletal System - 21%, Nervous System - 18%, Cardiovascular




System - 13%, Male Genitalia - 13%


250
LI:1144409.1:2000SEP08
Sense Organs - 53%


251
LI:246290.10:2000SEP08
Cardiovascular System - 29%, Female Genitalia - 29%


252
LI:280034.1:2000SEP08
Female Genitalia - 100%










[0306]

8


















SEQ ID NO:
Frame
Length
Start
Stop
GI Number
Probability
Score Annotation






















253
2
114
2
343
g11643582
2.00E−68
PR-domain containing protein 14


253
2
114
2
343
g10434076
2.00E−68
unnamed protein product


253
2
114
2
343
g7020503
4.00E−27
unnamed protein product


255
2
211
2
634
g7243243
2.00E−43
KIAA1431 protein


255
2
211
2
634
g4567178
2.00E−41
R31665_2 (AA 1-673)


255
2
211
2
634
g3445181
2.00E−41
R31665_2


256
3
151
54
506
g10433955
5.00E−40
unnamed protein product


256
3
151
54
506
g7295442
4.00E−14
CG17334 gene product


256
3
151
54
506
g2073111
3.00E−11
Y box protein 2


257
2
138
17
430
g12407395
4.00E−54
tripartite motif protein TRIM7


257
2
138
17
430
g12407397
2.00E−42
tripartite motif protein TRIM7


257
2
138
17
430
g12407379
8.00E−16
tripartite motif protein TRIM4 isoform beta


258
1
317
1
951
g9246977
1.00E−137
RNA-binding protein BRUNOL4


258
1
317
1
951
g12746394
1.00E−136
CUG-BP and ETR-3 like factor 4


258
1
317
1
951
g13278792
1.00E−106
Bruno (Drosophila)-like 4, RNA binding protein


260
2
114
14
355
g4589588
2.00E−34
KIAA0972 protein


260
2
114
14
355
g7576272
2.00E−30
bA393J16.1 (zinc finger protein 33a (KOX 31))


260
2
114
14
355
g498152
2.00E−30
ha0946 protein is Kruppel-related.


261
2
127
140
520
g10434195
2.00E−64
unnamed protein product


261
2
127
140
520
g13529188
4.00E−42
Unknown (protein for MGC: 12466)


261
2
127
140
520
g6467206
3.00E−36
gonadotropin inducible transcription repressor-4


262
1
151
1
453
g14042293
4.00E−47
unnamed protein product


262
1
151
1
453
g12052983
1.00E−46
hypothetical protein


262
1
151
1
453
g487785
7.00E−46
zinc finger protein ZNF136


263
1
79
16
252
g349075
4.00E−16
calmodulin-binding protein


263
1
79
16
252
g13543326
4.00E−16
hypothetical protein MGC8407


263
1
79
16
252
g12804937
4.00E−16
Unknown (protein for MGC: 3732)


264
1
183
112
660
g13325337
3.00E−83
Unknown (protein for MGC: 10520)


264
1
183
112
660
g8439407
3.00E−22
zinc finger protein


264
1
183
112
660
g7020166
3.00E−22
unnamed protein product


266
3
260
3
782
g12698001
1.00E−147
KIAA1728 protein


266
3
260
3
782
g8052233
1.00E−94
putative ankyrin-repeat containing protein


266
3
260
3
782
g7294632
2.00E−61
CG5679 gene product


267
2
196
2
589
g6249687
1.00E−108
P31155_1


267
2
196
2
589
g10436360
1.00E−53
unnamed protein product


267
2
196
2
589
g14042803
6.00E−50
unnamed protein product


268
1
113
130
468
g14596085
7.00E−55
(AY042830) Putative 40S ribosomal protein S15A


268
1
113
130
468
g9757906
7.00E−55
40S ribosomal protein S15A


268
1
113
130
468
g8439890
7.00E−55
Strong similarity to 40S ribosomal protein S15A









from Arabidopsis thallana gb|L27461. EST









gb|R30315 comes from this gene.


269
3
165
3
497
g12052983
2.00E−73
hypothetical protein


269
3
165
3
497
g5262560
1.00E−47
hypothetical protein


269
3
165
3
497
g10434856
1.00E−47
unnamed protein product


270
3
168
165
668
g12052983
4.00E−70
hypothetical protein


270
3
168
165
668
g5262560
4.00E−35
hypothetical protein


270
3
168
165
668
g10434856
5.00E−34
unnamed protein product


271
2
122
2
367
g12044553
8.00E−48
bA261P9.2 (putative novel protein similar to fly









CG7340 and human putative aminopeptidase









ZK353.6 in chromosome 3 (EC 3.4.11.-))


271
2
122
2
367
g10432867
5.00E−47
unnamed protein product


271
2
122
2
367
g7299691
5.00E−42
BcDNA: LD41548 gene product (alt 1)


272
2
91
212
484
g872315
3.00E−35
40S ribosomal protein S12


272
2
91
212
484
g12842004
3.00E−35
putative


272
2
91
212
484
g12833134
3.00E−35
putative


273
3
225
3
677
g510552
1.00E−100
ribosomal protein L13


273
3
225
3
677
g12833027
1.00E−99
putative


273
3
225
3
677
g3869148
4.00E−98
robosomal protein L13


274
3
153
3
461
g825539
2.00E−84
MLC2


274
3
153
3
461
g1675396
2.00E−84
myosin light chain 2


274
3
153
3
461
g1637
2.00E−84
myosin light chain 2 type 2


275
2
296
176
1063
g12407387
1.00E−147
tripartite motif protein TRIM5 isoform delta


275
2
296
176
1063
g12407385
1.00E−47
tripartite motif protein TRIM5 isoform gamma


275
2
296
176
1063
g12407383
1.00E−147
tripartite motif protein TRIM5 isoform beta


276
1
175
22
546
g13752754
1.00E−26
zinc finger 1111


276
1
175
22
546
g14348588
5.00E−25
KRAB zinc finger protein


276
1
175
22
546
g12654015
4.00E−24
Similar to hypothetical protein FLJ10891


277
3
76
141
368
g9714522
5.00E−13
bA162G10.3 (zinc finger protein)


277
3
76
141
368
g5730194
5.00E−13
KRAB protein domain


277
3
76
141
368
g4589588
8.00E−13
KIAA0972 protein


278
3
146
624
1061
g12697318
5.00E−14
PBX4 protein


278
3
146
624
1061
g7160798
9.00E−13
pbxy homeodomain protein


278
3
146
624
1061
g634053
9.00E−13
PBX2


279
3
391
3
1175
g10439850
1.00E−116
unnamed protein product


279
3
391
3
1175
g9968290
1.00E−112
zinc finger protein 304


279
3
391
3
1175
g14249844
1.00E−111
Similar to hypothetical protein FLJ23233


280
3
80
156
395
g12052983
7.00E−15
hypothetical protein


280
3
80
156
395
g13277768
1.00E−11
zinc finger protein 93


280
3
80
156
395
g1184371
1.00E−11
zinc finger protein; Method: conceptual









translation supplied by author


281
2
162
74
559
g6467206
8.00E−37
gonadotropin inducible transcription repressor-4


281
2
162
74
559
g9187356
2.00E−36
hypothetical protein, similar to (AB021644)









GONADOTROPIN INDUCIBLE









TRANSCRIPTION REPRESSOR-4


281
2
162
74
559
g220637
2.00E−36
zinc finger protein


282
2
164
50
541
g13752754
1.00E−28
zinc finger 1111


282
2
164
50
541
g14348588
5.00E−28
KRAB zinc finger protein


282
2
164
50
541
g12654015
3.00E−27
Similar to hypothetical protein FLJ10891


283
3
105
75
389
g12052732
2.00E−38
hypothetical protein


283
3
105
75
389
g3329372
9.00E−37
DNA-binding protein


283
3
105
75
389
g7959207
3.00E−34
KIAA1473 protein


284
1
123
289
657
g14042035
9.00E−64
unnamed protein product


284
1
123
289
657
g6224922
1.00E−41
BTB/POZ domain zinc finger factor HOF-S


284
1
123
289
657
g6063139
1.00E−41
BTB/POZ domain zinc finger factor HOF-L


285
1
174
199
720
g7022603
2.00E−20
unnamed protein product


285
1
174
199
720
g7022652
3.00E−10
unnamed protein product


285
1
174
199
720
g3283350
3.00E−08
calmodulin-binding protein SHA1


286
2
181
71
613
g13591714
4.00E−97
(AF343664) immunoglobulin superfamily









receptor translocation associated









protein 2c


286
2
181
71
613
g13591712
4.00E−97
(AF343663) immunoglobulin superfamily receptor









translocation









associated protein 2b


286
2
181
71
613
g13591710
4.00E−97
(AF343662) immunoglobulin superfamily receptor








translocation









associated protein 2a


287
1
91
64
336
g10047183
8.00E−48
KIAA1559 protein


287
1
91
64
336
g5080758
8.00E−25
BC331191_1


287
1
91
64
336
g456269
1.00E−21
zinc finger protein 30


288
1
188
226
789
g11999277
4.00E−45
solute carrier


288
1
188
226
789
g12845461
8.00E−34
putative


288
1
188
226
789
g10434874
2.00E−33
unnamed protein product


289
2
290
2
871
g14017771
1.00E−157
fibrillin3


289
2
290
2
871
g762831
1.00E−113
fibrillin 2


289
2
290
2
871
g4959652
1.00E−113
flbrillin-2


290
3
199
3
599
g3757719
1.00E−83
dJ422F24.1 (PUTATIVE novel protein









similar to C. elegans C0202.5)


290
3
199
3
599
g12832288
5.00E−83
putative


290
3
199
3
599
g7294769
2.00E−38
CG6279 gene product


291
3
148
3
446
g13489168
5.00E−77
60S ribosomal protein L17


291
3
148
3
446
g13430182
3.00E−76
ribosomal protein L17


291
3
148
3
446
g14596111
2.00E−75
(AY042843) 60S ribosomal protein L17


292
1
92
37
312
g6002102
5.00E−39
Acyl-CoA binding protein (ACBP)


292
1
92
37
312
g1938236
3.00E−38
acyl-CoA-binding protein


292
1
92
37
312
g6002104
2.00E−37
Acyl-CoA binding protein (ACBP)


293
3
256
3
770
g5091520
1.00E−127
ESTs AU058081(E30812), AU058365(E50679),









AU030138(E50679) correspond









to a region of the predicted gene.;









Similar to Spinacia oleracea mRNA for









proteasome 37 kD subunit, (X96974)


293
3
256
3
770
g8671496
1.00E−127
alpha 3 subunit of 20S proteasome


293
3
256
3
770
g8096329
1.00E−127
ESTs AU058081(E3082), AU075427









(E30384) correspond to a region of the









predicted gene, ˜Similar to Spinacia











oleracea
proteasome 27 kD subunit (P52427)



295
3
318
132
1085
g11602755
1.00E−37
zinc finger protein


295
3
318
132
1085
g12843135
6.00E−33
putative


295
3
318
132
1085
g13094151
3.00E−25
zinc finger protein hRit1 alpha


296
1
194
304
885
g12856559
1.00E−85
putative


296
1
194
304
885
g12856631
3.00E−85
putative


296
1
194
304
885
g12849896
3.00E−85
putative


297
1
469
1
1407
g9927838
0
unnamed protein product


297
1
469
1
1407
g10045028
0
unnamed protein product


297
1
469
1
1407
g10047295
1.00E−169
KIAA1610 protein


298
3
81
3
245
g13249093
5.00E−37
carbonic anhydrase XIII


298
3
81
3
245
g12845416
5.00E−37
putative


298
3
81
3
245
g65332
4.00E−22
carbonic anhydrase


299
1
452
1
1356
g11177164
0
polydom protein


299
1
452
1
1356
g12060830
1.00E−142
serologically defined breast cancer antigen









NY-BR-38


299
1
452
1
1356
g7292728
1.00E−52
fw gene product


300
1
362
97
1182
g14594722
0
(AY037298) elongation of very long chain fatty









acids protein


300
1
362
97
1182
g12044051
0
ELOVL4


300
1
362
97
1182
g12044043
0
ELOVL4


301
2
354
2
1063
g14272764
1.00E−146
unnamed protein product


301
2
354
2
1063
g561853
5.00E−28
megalin


301
2
354
2
1063
g1809240
7.00E−27
gp330 precursor


302
1
305
220
1134
g12483902
1.00E−83
zinc finger protein HIT-10


302
1
305
220
1134
g6002480
4.00E−49
BWSCR2 associated zinc-finger protein BAZ2


302
1
305
220
1134
g9963806
4.00E−47
zinc finger protein ZNF287


303
2
659
164
2140
g14587851
0
(AB050785) Graf2


303
2
659
164
2140
g13310137
0
PSGAP-m


303
2
659
164
2140
g13310135
0
PSGAP-s


304
3
390
102
1271
g13879442
1.00E−170
Similar to RIKEN cDNA 2310035M22 gene


304
3
390
102
1271
g12855490
1.00E−165
putative


304
3
390
102
1271
g12848905
1.00E−102
putative


305
2
294
2
883
g13898617
1.00E−142
serine/threonine protein kinase SSTK


305
2
294
2
883
g13540326
1.00E−142
serine/threonine kinase FKSG82


305
2
294
2
883
g13898619
1.00E−140
serine/threonine protein kinase SSTK


306
1
269
1
807
g14250138
1.00E−139
Similar to RIKEN cDNA 5730421E18 gene


306
1
269
1
807
g12856916
1.00E−120
putative


306
1
269
1
807
g12840367
1.00E−120
putative


307
3
270
393
1202
g10434082
1.00E−103
unnamed protein product


307
3
270
393
1202
g12052816
1.00E−102
hypothetical protein


307
3
270
393
1202
g297157
1.00E−74
rab17


308
3
358
150
1223
g12861800
1.00E−170
putative


308
3
358
150
1223
g3878713
5.00E−73
(Z46935) weak similarity with quinone









oxidoreductase, contains similarity to









Pfam domain: PF00107 (Zinc-binding









dehydrogenases), Score = −80.6, E-









value = 6.2e−06, N = 1˜cDNA









EST yk164b4.5 comes from this gene˜









cDNA EST yk164b4.3 comes from this









gene˜cDNA EST yk264f3.5 comes from









this


308
3
358
150
1223
g2633069
2.00E−52
similar to quinone oxidoreductase


309
2
232
2
697
g12834244
1.00E−71
putative


309
2
232
2
697
g12833174
1.00E−71
putative


309
2
232
2
697
g13905260
1.00E−36
RIKEN cDNA 1300006C06 gene


310
3
184
3
554
g2335037
9.00E−67
Tim17


310
3
184
3
554
g4378524
2.00E−65
mitochondrial inner membrane translocase









component Tlm17a


310
3
184
3
554
g12833600
2.00E−65
putative


311
1
206
46
663
g12314268
4.00E−82
dJ14N1.2 (novel S-100/ICaBP type calcium









binding domain protein, similar









to trichohyalin)


311
1
206
46
663
g553621
3.00E−14
profilaggrin


311
1
206
46
663
g12314267
3.00E−14
dJ14N1.1.1 (profilaggrin 5′ end)


312
2
301
59
961
g12314195
1.00E−171
bA255A11.3 (novel protein similar to KIAA1074)


312
2
301
59
961
g12314164
1.00E−134
bA526D8.2 (novel protein similar to KIAA1074)


312
2
301
59
961
g12053099
4.00E−95
hypothetical protein


313
1
156
70
537
g6692607
2.00E−65
MGA protein


313
1
156
70
537
g5931585
1.00E−44
T-box family member; T-box domain


313
1
156
70
537
g4049463
4.00E−16
transcription factor TBX6


314
1
279
340
1176
g12854977
1.00E−123
putative


314
1
279
340
1176
g7267246
1.00E−41
putative adenosine deaminase


314
1
279
340
1176
g7299138
2.00E−39
CG11994 gene product


315
1
329
181
1167
g4582324
0
dJ708F5.1 (PUTATIVE novel Collagen alpha 1









LIKE protein)


315
1
329
181
1167
g12052774
0
hypothetical protein


315
1
329
181
1167
g2326442
1.00E−38
collagen type XII alpha 1 chain


316
3
757
3
2273
g8896164
0
kinesin-like protein GAKIN


316
3
757
3
2273
g10697238
0
KIF13A


316
3
757
3
2273
g12054032
0
KINESIN-13A2


317
1
329
1
987
g14595658
8.00E−97
(AF387815) LIM protein prickle


317
1
329
1
987
g9229890
3.00E−84
prickle 2


317
1
329
1
987
g9229888
3.00E−83
prickle 1


318
1
494
1
1482
g1763096
0
glutamate pyruvate transaminase


318
1
494
1
1482
g467528
0
alanine aminotransferase


318
1
494
1
1482
g1507680
0
alanine aminotransferase


319
1
156
400
867
g5912051
2.00E−30
hypothetical protein


319
1
156
400
867
g14278937
2.00E−30
calmin


319
1
156
400
867
g10437695
2.00E−30
unnamed protein product


320
1
128
118
501
g7294107
4.00E−44
CG4638 gene product


320
1
128
118
501
g3169065
3.00E−40
elongation factor 2-like protein


320
1
128
118
501
g1302132
4.00E−38
ORF YNL163c


321
1
197
151
741
g13185203
2.00E−21
unnamed protein product


321
1
197
151
741
g2463632
3.00E−14
monocarboxylate transporter homologue MCT6


321
1
197
151
741
g6103363
3.00E−13
monocarboxylate transporter MCT3


322
1
560
1
1680
g4240293
1.00E−141
KIAA0902 protein


322
1
560
1
1680
g4151807
1.00E−141
membrane-associated guanylate kinase-









interacting protein 2 Maguin-2


322
1
560
1
1680
g4151805
1.00E−141
membrane-associated guanylate kinase-









interacting protein 1 Maguin-1


323
2
163
2
490
g10172680
3.00E−06
stage V sporulation protein C









(peptidyl-tRNA hydrolase)


323
2
163
2
490
g1001232
4.00E−06
(D64003) peptidyl-tRNA hydrolase


323
2
163
2
490
g2983032
1.00E−05
peptidyl-tRNA hydrolase


324
2
197
2
592
g9295345
2.00E−67
HSKM-B


324
2
197
2
592
g12834773
5.00E−19
putative


324
2
197
2
592
g5870834
3.00E−17
skm-BOP2


325
3
520
3
1562
g8655678
1.00E−139
hypothetical protein


325
3
520
3
1562
g12382779
1.00E−59
zinc transporter 1


325
3
520
3
1562
g577843
2.00E−59
ZnT-1


326
1
772
640
2955
g13358642
0
hypothetical protein


326
1
772
640
2955
g10435064
0
unnamed protein product


326
1
772
640
2955
g10434826
0
unnamed protein product


327
3
702
153
2258
g7264026
0
dJ876B10.2 (novel protein (ortholog of rat









EXO84))


327
3
702
153
2258
g2827164
0
exo84


327
3
702
153
2258
g7301432
2.00E−38
CG6095 gene product


328
3
255
609
1373
g13383265
1.00E−106
actin related protein


328
3
255
609
1373
g13938319
1.00E−105
Unknown (protein for MGC: 15664)


328
3
255
609
1373
g12840619
9.00E−72
putative


330
2
178
203
736
g10435210
2.00E−76
unnamed protein product


330
2
178
203
736
g14598968
3.00E−58
(AX179297) 21615 ADH


330
2
178
203
736
g8895083
3.00E−58
oxidoreductase UCPA


331
1
217
1624
2274
g8655648
1.00E−108
hypothetical protein


331
1
217
1624
2274
g12803319
1.00E−108
Unknown (protein for MGC: 3090)


331
1
217
1624
2274
g10047337
1.00E−108
KIAA1630 protein


332
1
191
823
1395
g9651711
4.00E−72
arsenite inducible RNA associated protein


332
1
191
823
1395
g12835478
3.00E−53
putative


332
1
191
823
1395
g7295806
6.00E−45
CG12795 gene product


333
2
252
1223
1978
g12856598
6.00E−93
putative


333
2
252
1223
1978
g14042913
2.00E−19
unnamed protein product


333
2
252
1223
1978
g14424618
9.00E−19
hypothetical protein MGC2628


334
2
502
305
1810
g12845866
1.00E−131
putative


334
2
502
305
1810
g13477235
4.00E−80
Similar to RIKEN cDNA 0610037N03 gene


334
2
502
305
1810
g12833017
6.00E−22
putative


335
2
369
2
1108
g12856270
1.00E−165
putative


335
2
369
2
1108
g6682873
1.00E−119
reduced expression in cancer


335
2
369
2
1108
g7230612
1.00E−116
small rec


337
2
332
2
997
g8886025
1.00E−166
collapsin response mediator protein-5


337
2
332
2
997
g8671168
1.00E−166
hypothetical protein


337
2
332
2
997
g13259169
1.00E−166
phosphoprotein ULIP6


338
1
215
73
717
g12652727
1.00E−125
Unknown (protein for IMAGE: 3352566)


338
1
215
73
717
g488555
2.00E−67
zinc finger protein ZNF135


338
1
215
73
717
g8050899
6.00E−65
ZNF180


339
3
364
3
1094
g9758769
1.00E−64
11-beta-hydroxysteroid dehydrogenase-like


339
3
364
3
1094
g8777393
1.00E−64
11-beta-hydroxysteroid dehydrogenase-like


339
3
364
3
1094
g8777400
1.00E−54
contains similarity to oxidoreductase˜









gene_id: MFB16.17


340
3
229
21
707
g12052959
1.00E−130
hypothetical protein


340
3
229
21
707
g14336767
1.00E−128
similar to









homoprotocatechuate catabolism bifunctional









isomerase/decarboxylase


340
3
229
21
707
g7670464
1.00E−115
unnamed protein product


341
1
164
235
726
g2286123
8.00E−47
testis specific DNAj-homolog


341
1
164
235
726
g12838392
8.00E−47
putative


341
1
164
235
726
g12838396
4.00E−46
putative


342
1
131
199
591
g12804323
5.00E−60
Unknown (protein for MGC: 4054)


342
1
131
199
591
g3264773
5.00E−32
zinc-finger protein-37; ZFP-37


342
1
131
199
591
g10440398
5.00E−32
FLJ00032 protein


343
2
406
701
1918
g12697482
1.00E−121
dJ583P15.7.2 (novel zinc finger









protein similar to rat RIN ZF)


343
2
406
701
1918
g12855580
1.00E−81
putative


343
2
406
701
1918
g12847599
7.00E−78
putative


344
3
219
3
659
g6091722
3.00E−51
putative ribosomal protein L13


344
3
219
3
659
g6650751
2.00E−49
ribosomal protein I


344
3
219
3
659
g2984157
4.00E−28
ribosomal protein L13


345
2
134
95
496
g14042747
4.00E−63
unnamed protein product


345
2
134
95
496
g10440516
4.00E−63
FLJ00106 protein


345
2
134
95
496
g10445215
7.00E−62
PDZ-LIM protein mystique


346
3
174
3
524
g11527997
1.00E−112
NOTCH2 protein


346
3
174
3
524
g11275978
1.00E−112
NOTCH 2


346
3
174
3
524
g287990
1.00E−112
Motch B


347
1
306
202
1119
g14024759
4.00E−32
aldehyde dehydrogenase


347
1
306
202
1119
g13162101
3.00E−28
putative aldehyde dehydrogenase


347
1
306
202
1119
g14025513
1.00E−23
succinate-semialdehyde dehydrogenase


348
3
283
819
1667
g10438978
1.00E−156
unnamed protein product


348
3
283
819
1667
g13358630
1.00E−155
hypothetical protein


348
3
283
819
1667
g9280094
1.00E−36
unnamed protein product


349
3
188
123
686
g4126809
5.00E−88
glyoxalase I


349
3
188
123
686
g1808684
3.00E−84
hypothetical protein


349
3
188
123
686
g2213425
8.00E−81
hypothetical protein


350
1
176
1
528
g57469
2.00E−98
vasopressin


350
1
176
1
528
g4469315
2.00E−98
vasopressin precursor


350
1
176
1
528
g207674
3.00E−96
vasopressin/neurophysin precursor


351
1
52
253
408
g3790135
3.00E−18
dJ191N21.3 (proteasome subunit HC5)


351
1
52
253
408
g220026
3.00E−18
proteasome subunit C5


351
1
52
253
408
g1698584
3.00E−18
proteasome beta-subunit C5


352
3
190
3
572
g205662
5.00E−86
nucleoside diphosphate kinase


352
3
190
3
572
g206580
4.00E−85
RBL-NDP kinase 18 kDa subunit (p18)


352
3
190
3
572
g53354
5.00E−85
nucleoside diphosphate kinase B


353
3
135
546
950
g9368839
1.00E−37
hypothetical protein


353
3
135
546
950
g57690
9.00E−29
ribosomal protein L23a


353
3
135
546
950
g404015
9.00E−29
ribosomal protein L23a


354
1
517
1
1551
g13161184
0
cytochrome P450 2S1


354
1
517
1
1551
g14042396
0
unnamed protein product


354
1
517
1
1551
g12836063
0
putative


355
2
135
203
607
g7677318
5.00E−55
aldehyde reductase


355
2
135
203
607
g12848322
5.00E−55
putative


355
2
135
203
607
g12848318
5.00E−55
putative


356
3
77
42
272
g3851089
1.00E−24
guanine nucleotide binding protein gamma 5


356
3
77
42
272
g3329380
1.00E−24
G protein gamma 5 subunit


356
3
77
42
272
g204241
1.00E−24
G protein gamma-5 subunit


357
3
110
96
425
g7340072
4.00E−15
40S ribosomal protein S15A


357
3
110
96
425
g495273
4.00E−15
ribosomal protein S15a


357
3
110
96
425
g12859337
4.00E−15
putative


358
1
485
1
1455
g10436300
0
unnamed protein product


358
1
485
1
1455
g10433852
0
unnamed protein product


358
1
485
1
1455
g9280029
0
unnamed protein product


360
1
143
1
429
g63466
2.00E−56
histone H2A


360
1
143
1
429
g6094631
2.00E−56
histone H2A.F


360
1
143
1
429
g3420799
2.00E−56
histone H2A.F/Z variant


361
3
81
159
401
g10437078
4.00E−34
unnamed protein product


361
3
81
159
401
g12859774
600E−33
putative


361
3
81
159
401
g12857408
6.00E−33
putative


362
3
543
834
2462
g12849316
4.00E−87
putative


362
3
543
834
2462
g6164628
3.00E−86
SH3 and PX domain-containing protein SH3PX1


362
3
543
834
2462
g5410249
3.00E−86
SDP1 protein


363
1
185
1
555
g12836716
1.00E−103
putative


363
1
185
1
555
g12834312
1.00E−103
putative


363
1
185
1
555
g12832330
1.00E−103
putative


364
3
156
177
644
g14456629
1.00E−31
dJ54B20.2 (novel KRAB box containing









C2H2 type zinc finger protein)


364
3
156
177
644
g4589588
9.00E−27
KIAA0972 protein


364
3
156
177
644
g3970712
3.00E−23
zinc finger protein 10


365
1
183
235
783
g12248382
7.00E−31
SEMB


365
1
183
235
783
g854326
7.00E−29
semaphorin B


365
1
183
235
783
g1110599
1.00E−14
semaphorin homolog = M-Sema F









(mice, neonatal brain, Peptide, 834 aa)


366
1
416
1
1248
g13543419
1.00E−161
Similar to zinc finger protein 304


366
1
416
1
1248
g7020745
5.00E−53
unnamed protein product


366
1
416
1
1248
g12652759
5.00E−53
hypothetical protein FLJ20557


367
2
258
455
1228
g1174187
2.00E−94
purine nucleotide binding protein


367
2
258
455
1228
g193444
8.00E−88
guanylate binding protein


367
2
258
455
1228
g829177
1.00E−68
guanylate binding protein isoform II


368
3
68
270
473
g14586963
7.00E−10
(AF362574) M75


368
3
68
270
473
g57115
7.00E−10
ribosomal protein L31 (AA 1-125)


368
3
68
270
473
g36130
7.00E−10
ribosomal protein L31 (AA 1-125)


371
1
122
568
933
g10435150
2.00E−39
unnamed protein product


371
1
122
568
933
g4982195
2.00E−16
lepA protein


371
1
122
568
933
g2984041
6.00E−16
G-protein LepA


372
3
111
3
335
g13752754
3.00E−15
zinc finger 1111


372
3
111
3
335
g7023216
2.00E−14
unnamed protein product


372
3
111
3
335
g14348588
2.00E−14
KRAB zinc finger protein


373
3
1281
36
3878
g157409
2.00E−95
fat protein


373
3
1281
36
3878
g7295732
3.00E−94
ft gene product


373
3
1281
36
3878
g10727403
2.00E−93
ds gene product


374
3
164
3
494
g9759463
2.00E−60
40S ribosomal protein S19


374
3
164
3
494
g6513924
4.00E−60
putative 40S ribosomal protein S19


374
3
164
3
494
g13878029
4.00E−60
putative 40S ribosomal protein S19


375
3
365
750
1844
g55628
0
reading frame (preproalbumin)


375
3
365
750
1844
g3647327
0
serum albumin


375
3
365
750
1844
g12845183
0
putative


376
1
96
184
471
g12853416
5.00E−25
putative


376
1
96
184
471
g13529497
8.00E−23
Unknown (protein for MGC: 6652)


376
1
96
184
471
g4589588
5.00E−22
KIAA0972 protein


377
2
106
125
442
g14042293
3.00E−37
unnamed protein product


377
2
106
125
442
g12052983
3.00E−37
hypothetical protein


377
2
106
125
442
g14043841
7.00E−34
Unknown (protein for MGC: 14429)


378
2
119
2
358
g57710
2.00E−31
ribosomal phosphoprotein P1 (AA 1-114)


378
2
119
2
358
g190234
2.00E−31
acidic ribosomal phosphoprotein (P1)


378
2
119
2
358
g14043204
2.00E−31
ribosomal protein, large, P1


380
2
282
2
847
g10440398
8.00E−93
FLJ00032 protein


380
2
282
2
847
g10047297
8.00E−93
KIAA1611 protein


380
2
282
2
847
g10436789
6.00E−92
unnamed protein product


381
2
47
287
427
g7290056
2.00E−10
EG: 118B3.2 gene product (alt 2)


381
2
47
287
427
g5901822
2.00E−10
EG: 118B3.2


381
2
47
287
427
g3645991
2.00E−10
/prediction = (method: ““genefinder””,









version: ““084””,









score: ““128.32””)˜/









prediction = (method: ““genscan””,









version: ““1.0””)˜/









match = (desc: ““KIAA0376 PROTEIN









(FRAGMENT)””, species: ““HOMO











SAPIENS
(HUMAN)””,










ranges: (query:15779 . . . 16030,









target: SPTREMBL::O15081:314 . . . 231,









score: ““229.00””),









(query:14786 . . . 15736,









target: SPTREMBL::O15081: 650 . . . 334,









score: ““319.00””),









(query: 13868 . . . 13960,









target: SPTREMBL::O15081: 884 . . . 854,









score:““156.00””)),









method: ““blastx””,









version: ““1.4.9””)˜/









match = (desc: ““SPECTRIN









BETA CHAIN, ERYTHROCYTE””,









species: ““HOMO SAPIENS (HUMAN)









””, ranges: (query: 13748 . . . 13954,









target: SWISS-PROT::P11277: 242 . . . 174,









score: ““201.00””)),









method:““blastx””,









version: ““1.4.9””)˜/









match = (desc: ““









GH04661.5prime GH Drosophila









melanogaster head pOT2 Drosophila









melanogaster cDNA clone GH046615









prime, mRNA sequence””,









species: ““Drosophila melanogaster (fruit fly)””,









ranges: (query: 22139 . . . 22499,









target: EMBL::AI064293: 361 . . . 1,









score: ““1796.00””)),









method: ““blastn””,









version: ““1.4.9””)˜/









match = (desc: ““GH05563.5prime









GH Drosophila









melanogaster head pOT2 Drosophila









melanogaster cDNA clone GH05563


383
1
280
16
855
g14456629
9.00E−90
dJ54B20.2









(novel KRAB box containing









C2H2 type zinc finger protein)


383
1
280
16
855
g3378094
3.00E−72
KRAB domain zinc finger protein


383
1
280
16
855
g1020145
1.00E−71
DNA binding protein


384
3
264
3
794
g6807587
1.00E−124
hypothetical protein


384
3
264
3
794
g5931821
1.00E−124
dJ228H13.3 (zinc finger protein)


384
3
264
3
794
g488555
1.00E−96
zinc finger protein ZNF135


385
3
561
135
1817
g10954044
0
KRAB zinc finger protein ZFQR


385
3
561
135
1817
g10442700
0
zinc-finger protein ZBRK1


385
3
561
135
1817
g10435411
0
unnamed protein product


386
2
288
206
1069
g10439850
4.00E−70
unnamed protein product


386
2
288
206
1069
g4894364
6.00E−64
zinc finger protein 3


386
2
288
206
1069
g12655165
6.00E−64
zinc finger protein 256


387
3
476
171
1598
g14042538
0
unnamed protein product


387
3
476
171
1598
g10438630
0
unnamed protein product


387
3
476
171
1598
g13096919
0
Similar to zinc finger protein 135 (clone pHZ-17)


389
3
60
78
257
g5262560
5.00E−07
hypothetical protein


389
3
60
78
257
g10434856
5.00E−07
unnamed protein product


389
3
60
78
257
g13623354
6.00E−07
Similar to zinc finger protein 136 (clone pHZ-20)


390
2
355
254
1318
g10047183
1.00E−94
KIAA1559 protein


390
2
355
254
1318
g13676461
6.00E−81
hypothetical protein


390
2
355
254
1318
g4589566
1.00E−80
KIAA0961 protein


391
1
101
112
414
g13937999
3.00E−48
Similar to DNA-binding protein


391
1
101
112
414
g3329372
1.00E−34
DNA-binding protein


391
1
101
112
414
g12052732
3.00E−34
hypothetical protein


392
3
326
3
980
g14017921
0
KIAA1852 protein


392
3
326
3
980
g8050899
1.00E−133
ZNF180


392
3
326
3
980
g6409345
1.00E−133
zinc finger protein ZNF180


393
3
263
792
1580
g5441615
1.00E−96
zinc finger protein


393
3
263
792
1580
g498721
1.00E−94
zinc finger protein


393
3
263
792
1580
g8099348
2.00E−93
zinc finger protein


394
3
121
372
734
g10439850
3.00E−18
unnamed protein product


394
3
121
372
734
g14249844
7.00E−18
Similar to hypothetical protein FLJ23233


394
3
121
372
734
g2689441
4.00E−13
F18547_1


395
2
298
2
895
g10437560
0
unnamed protein product


395
2
298
2
895
g10047305
0
KIAA1615 protein


395
2
298
2
895
g498721
4.00E−86
zinc finger protein


396
1
287
220
1080
g14042550
3.00E−94
unnamed protein product


396
1
287
220
1080
g13937909
3.00E−94
Similar to KIAA0961 protein


396
1
287
220
1080
g10047183
5.00E−78
KIAA1559 protein


397
1
281
277
1119
g3540177
1.00E−123
F23269_2


397
1
281
277
1119
g5080758
1.00E−120
BC331191_1


397
1
281
277
1119
g12855931
5.00E−73
putative


398
1
263
1
789
g10434650
4.00E−88
unnamed protein product


398
1
263
1
789
g13623217
2.00E−40
Similar to hypothetical protein FLJ12895


398
1
263
1
789
g7020855
6.00E−27
unnamed protein product


399
2
646
200
2137
g14042373
0
unnamed protein product


399
2
646
200
2137
g498152
0
ha0946 protein is Kruppel-related.


399
2
646
200
2137
g7243633
0
RB-associated KRAB repressor


400
2
199
140
736
g204123
5.00E−89
ferritin light chain


400
2
199
140
736
g204133
6.00E−89
ferritin light chain


400
2
199
140
736
g193275
6.00E−89
ferritin light chain


401
1
210
25
654
g9651704
4.00E−79
carboxypeptidase B precursor


401
1
210
25
654
g6013463
8.00E−61
carboxypeptidase homolog


401
1
210
25
654
g203295
8.00E−61
carboxypeptidase B


402
2
390
2
1171
g13365901
0
hypothetical protein


402
2
390
2
1171
g2104689
1.00E−126
alpha glucosidase II, alpha subunit


402
2
390
2
1171
g1890664
1.00E−126
glucosidase II


403
3
43
348
476
g12052884
3.00E−06
hypothetical protein


403
3
43
348
476
g7023332
4.00E−06
unnamed protein product


403
3
43
348
476
g183002
6.00E−05
guanylate binding protein isoform I


404
1
406
1
1218
g12053281
0
hypothetical protein


404
1
406
1
1218
g12836135
1.00E−167
putative


404
1
406
1
1218
g3043598
2.00E−64
KIAA0537 protein


405
1
90
1
270
g7981261
4.00E−33
dJ50O24.4 (novel protein with DHHC









zinc finger domain)


405
1
90
1
270
g14035816
4.00E−33
unnamed protein product


405
1
90
1
270
g12224992
4.00E−33
hypothetical protein


407
2
192
44
619
g7297667
1.00E−30
CG5022 gene product


407
2
192
44
619
g2224617
4.00E−30
KIAA0338


407
2
192
44
619
g13277297
4.00E−30
bA234K24.1.2 (Erythrocyte membrane









protein band 4.1-like 1 protein









(KIAA0338) Isoform 2)


408
1
183
28
576
g12314083
9.00E−94
dJ1007G16.5 (novel high-mobility









group (nonhistone chromosomal)









protein 2 (HMG2) like protein)


408
1
183
28
576
g12838247
4.00E−67
putative


408
1
183
28
576
g1304193
9.00E−35
HMG2


409
3
163
3
491
g12697320
8.00E−51
Pbx4 protein


409
3
163
3
491
g7160800
3.00E−50
Pbx4/Lazarus homeodomain protein


409
3
163
3
491
g5679283
3.00E−50
Pbx4 homeodomain protein


410
3
186
198
755
g12840673
2.00E−48
putative


410
3
186
198
755
g607003
4.00E−18
beta transducin-like protein


410
3
186
198
755
g3878300
1.00E−14
predicted using Genefinder˜Similarity









to C.elegans Guanine nucleotide









binding protein (WP: C14B1.4),









contains similarity to Pfam domain: PF00400









(WD domain, G-beta repeat), Score = 196.1,









E-value = 1.8e−55, N = 7˜cDNA









EST yk567g12.3 comes from this









gene˜cDNA EST yk567g12.5 comes from









this gene


411
1
134
286
687
g11342541
2.00E−67
putative white family ATP-binding









cassette transporter


411
1
134
286
687
g9665220
3.00E−50
ATP-binding cassette transporter,









sub-family G member 1


411
1
134
286
687
g7768742
3.00E−50
white protein homolog (ATP-binding









cassette transporter 8)


412
2
97
35
325
g57175
1.00E−37
S-100 protein


412
2
97
35
325
g206825
1.00E−37
S100 protein


412
2
97
35
325
g404769
2.00E−37
S100 beta protein


413
1
181
1
543
g13543071
9.00E−64
RIKEN cDNA 1500031N16 gene


413
1
181
1
543
g12837801
9.00E−64
putative


413
1
181
1
543
g12832973
5.00E−60
putative


414
3
258
3
776
g12856949
4.00E−98
putative


414
3
258
3
776
g12653785
3.00E−97
Unknown (protein for IMAGE: 3349601)


414
3
258
3
776
g12845723
4.00E−94
putative


415
2
169
2
508
g7259240
1.00E-79
unnamed protein product


415
2
169
2
508
g12845457
1.00E−79
putative


415
2
169
2
508
g12834293
1.00E−79
putative


416
1
177
310
840
g9502403
5.00E−06
Hypothetical zinc finger-like protein


417
1
81
451
693
g14042550
6.00E−27
unnamed protein product


417
1
81
451
693
g13937909
6.00E−27
Similar to KIAA0961 protein


417
1
81
451
693
g487787
3.00E−23
zinc finger protein ZNF140


418
2
94
329
610
g13752754
7.00E−18
zinc finger 1111


418
2
94
329
610
g14348588
1.00E−16
KRAB zinc finger protein


418
2
94
329
610
g12654015
1.00E−16
Similar to hypothetical protein FLJ10891


419
3
165
3
497
g12856090
2.00E−51
putative


419
3
165
3
497
g12854104
2.00E-51
putative


419
3
165
3
497
g4678718
4.00E−43
dJ2013.1 (brain mitochondrial carrier









protein-1 (BMCP1))


420
3
352
111
1166
g13444976
4.00E−36
unnamed protein product


420
3
352
111
1166
g12309630
4.00E−36
bA438B23.1 (neuronal leucine-rich









repeat protein)


420
3
352
111
1166
g9651089
8.00E−34
hypothetical protein


421
2
113
2
340
g14164613
3.00E−27
sialic acid binding immunoglobulin-like









lectin 10


421
2
113
2
340
g13991167
6.00E−16
sialic acid-binding immunoglobulin-like









lectin-like long splice variant


421
2
113
2
340
g13991166
6.00E−16
sialic acid-binding immunoglobulin-like









lectin-like short splice variant


422
2
100
101
400
g12052732
1.00E−38
hypothetical protein


422
2
100
101
400
g3329372
8.00E−37
DNA-binding protein


422
2
100
101
400
g7959207
2.00E−34
KIAA1473 protein


423
1
117
1
351
g7959207
800E−39
KIAA1473 protein


423
1
117
1
351
g3342002
2.00E−36
hematopoietic cell derived zinc finger protein


423
1
117
1
351
g186774
5.00E−35
zinc finger protein


424
2
250
2
751
g14042850
2.00E−50
unnamed protein product


424
2
250
2
751
g12052983
8.00E−37
hypothetical protein


424
2
250
2
751
g14042293
1.00E−36
unnamed protein product


425
1
199
1
597
g10437560
1.00E−105
unnamed protein product


425
1
199
1
597
g10047305
1.00E−105
KIAA1615 protein


425
1
199
1
597
g13436440
2.00E−77
Unknown (protein for MGC: 4400)


426
3
166
3
500
g14017833
3.00E−86
KIAA1808 protein


426
3
166
3
500
g4240175
6.00E−24
KIAA0843 protein


426
3
166
3
500
g505094
5.00E−21
similar to an actin bundling protein, dematn.


427
1
157
1168
1638
g14042421
4.00E−11
unnamed protein product


427
1
157
1168
1638
g14017937
4.00E−11
KIAA1860 protein


427
1
157
1168
1638
g13366084
4.00E−11
MAP/microtubule affinity-regulating kinase like 1


429
3
200
3
602
g9651099
1.00E−118
hypothetical protein


429
3
200
3
602
g881564
1.00E−55
ZNF157


429
3
200
3
602
g453466
5.00E−55
zinc finger protein


430
2
173
2
520
g11990770
2.00E−67
bA534G20.1.1 (novel protein similar to









Lysozyme C-1 (1,4-beta-N-









acylmuramidase C, EC 3.2.1.17) (isoform 1))


430
2
173
2
520
g11990771
1.00E−56
bA534G20.1.2 (novel protein similar to









Lysozyme C-1 (1,4-beta-N-









acylmuramidase C, EC 3.2.1.17) (isoform 2))


430
2
173
2
520
g12839824
3.00E−49
putative


431
1
181
76
618
g13591714
4.00E−97
(AF343664) immunoglobulin









superfamily receptor translocation









associated protein 2c


431
1
181
76
618
g13591712
4.00E−97
(AF343663) immunoglobulin









superfamily receptor translocation









associated protein 2b


431
1
181
76
618
g13591710
4.00E−97
(AF343662) immunoglobulin









superfamily receptor translocation









associated protein 2a


433
1
157
22
492
g7268562
7.00E−54
ribosomal protein L32-like protein


433
1
157
22
492
g5816996
7.00E−54
ribosomal protein L32-like protein


433
1
157
22
492
g13899057
2.00E−53
ribosomal protein L32


434
1
182
157
702
g12855141
5.00E−89
putative


434
1
182
157
702
g12852338
5.00E−89
putative


434
1
182
157
702
g12849745
5.00E−89
putative


435
2
134
2
403
g2624328
2.00E−44
OsGRP2


435
2
134
2
403
g2366750
2.00E−34
RNA binding protein


435
2
134
2
403
g7268089
8.00E−34
glycine-rich RNA-binding protein AtGRP2-like


436
2
148
731
1174
g13397122
1.00E−58
unnamed protein product


436
2
148
731
1174
g12654715
1.00E−58
Similar to glucose regulated protein, 58 kDa


436
2
148
731
1174
g10728195
3.00E−15
CG1837 gene product


437
2
296
2
889
g12597312
1.00E−149
tRNA-guanine transglycosylase


437
2
296
2
889
g12597314
1.00E−137
tRNA-guanine transglycosylase


437
2
296
2
889
g7415812
1.00E−135
tRNA-guanine transglycosylase


438
3
169
9
515
g12406772
4.00E−52
unnamed protein product


438
3
169
9
515
g12406688
4.00E−52
unnamed protein product


438
3
169
9
515
g7299372
4.00E−29
CG6567 gene product


439
2
170
200
709
g14133251
3.00E−93
KIAA1479 protein


439
2
170
200
709
g2623162
7.00E−39
semaphorin VIa


439
2
170
200
709
g11093909
7.00E−39
axon guidance signal SEMA6A1


440
2
841
2
2524
g11177164
0
polydom protein


440
2
841
2
2524
g12060830
1.00E−155
serologically defined breast









cancer antigen NY-BR-38


440
2
841
2
2524
g14198157
4.00E−83
polydomain protein


441
1
271
70
882
g13898617
1.00E−142
serine/threonine protein kinase SSTK


441
1
271
70
882
g13540326
1.00E−142
serine/threonine kinase FKSG82


441
1
271
70
882
g13898619
1.00E−140
serine/threonine protein kinase SSTK


442
2
311
743
1675
g8979743
1.00E−160
Band4.1-like5 protein


442
2
311
743
1675
g13278193
1.00E−153
Similar to EHM2 gene


442
2
311
743
1675
g10434740
1.00E−140
unnamed protein product


443
2
529
416
2002
g12834087
1.00E−155
putative


443
2
529
416
2002
g2463628
6.00E−46
putative monocarboxylate transporter


443
2
529
416
2002
g7328162
1.00E−40
hypothetical protein


444
1
335
4
1008
g13159480
1.00E−128
Translation may initiate at the ATG









codon at nucleotides 40-42 or the ATG









at nucleotides 43-45


444
1
335
4
1008
g9229906
5.00E−35
fibrinogen-like protein


444
1
335
4
1008
g387156
8.00E−33
fibrinogen-like protein


445
1
329
196
1182
g4582324
0
dJ708F5.1 (PUTATIVE novel Collagen









alpha 1 LIKE protein)


445
1
329
196
1182
g12052774
0
hypothetical protein


445
1
329
196
1182
g2326442
1.00E−38
collagen type XII alpha 1 chain


446
2
395
110
1294
g12642596
0
nuclear receptor co-repressor/









HDAC3 complex subunit TBLR1


446
2
395
110
1294
g10434648
0
unnamed protein product


446
2
395
110
1294
g12006104
0
IRA1


447
1
163
1
489
g12858551
7.00E−67
putative


447
1
163
1
489
g12805285
7.00E−67
Similar to ribosomal protein S27a


447
1
163
1
489
g1050756
7.00E−67
fusion protein: ubiquitin (bases 43_513);









ribosomal protein S27a (bases









217_532)


448
3
78
330
563
g8699209
5.00E−06
cyclophilin A


448
3
78
330
563
g50621
5.00E−06
cyclophilin (AA 1-164)


448
3
78
330
563
g49496
5.00E−06
cyclophilin (AA 1-164)


449
1
314
277
1218
g12844770
1.00E−130
putative


449
1
314
277
1218
g12861366
1.00E−127
putative


449
1
314
277
1218
g12857383
7.00E−50
putative


450
1
130
181
570
g2843171
4.00E−06
zinc finger protein


450
1
130
181
570
g5817149
5.00E−06
hypothetical protein


450
1
130
181
570
g10434142
5.00E−06
unnamed protein product


451
1
176
697
1224
g13383265
1.00E−63
actin related protein


451
1
176
697
1224
g13938319
3.00E−62
Unknown (protein for MGC: 15664)


451
1
176
697
1224
g12840619
2.00E−51
putative


452
3
671
3
2015
g12698057
1.00E−168
KIAA1756 protein


452
3
671
3
2015
g1177322
1.00E−124
CPG2 protein


452
3
671
3
2015
g10728577
1.00E−82
Msp-300 gene product


453
3
293
3
881
g4235148
8.00E−85
BC41195_1


453
3
293
3
881
g14165525
7.00E−71
Similar to CG8500 gene product


453
3
293
3
881
g14388336
2.00E−70
hypothetical protein


455
1
253
478
1236
g14424576
1.00E−118
hypothetical protein FLJ21963


455
1
253
478
1236
g10438188
1.00E−118
unnamed protein product


455
1
253
478
1236
g14025162
3.00E−57
acetyl-coa synthetase


457
1
125
529
903
g12859335
1.00E−26
putative


457
1
125
529
903
g12858578
1.00E−26
putative


457
1
125
529
903
g12843085
6.00E−21
putative


458
1
394
577
1758
g14533376
1.00E−148
(AX151207) unnamed protein product


458
1
394
577
1758
g11762100
1.00E−144
myo-inositol 1-phosphate synthase


458
1
394
577
1758
g3108053
1.00E−144
myo-inositol 1-phosphate synthase; INO1


459
3
149
1137
1583
g12053149
2.00E−39
hypothetical protein


460
2
323
122
1090
g7297059
3.00E−06
CG9117 gene product


461
3
200
387
986
g13365897
1.00E−82
hypothetical protein


461
3
200
387
986
g2636109
2.00E−24
similar to metabolite transport









protein


461
3
200
387
986
g1894771
2.00E−24
product highly similar to









metabolite transport proteins


462
2
406
701
1918
g12697482
1.00E−121
dJ583P15.7.2 (novel zinc finger protein









similar to rat RIN ZF)


462
2
406
701
1918
g12855580
1.00E−81
putative


462
2
406
701
1918
g12847599
7.00E−78
putative


463
3
181
102
644
g13879442
2.00E−78
Similar to RIKEN cDNA 2310035M22 gene


463
3
181
102
644
g12848905
2.00E−78
putative


463
3
181
102
644
g12855490
1.00E−73
putative


464
3
137
69
479
g11231085
7.00E−29
hypothetical protein


464
3
137
69
479
g10998425
6.00E−09
NORPEG-like protein


464
3
137
69
479
g10937641
6.00E−09
ankycorbin


465
2
278
218
1051
g12861800
1.00E−111
putative


465
2
278
218
1051
g3878713
2.00E−38
(Z46935) weak similarity with quinone









oxidoreductase, contains similarity









to Pfam domain: PF00107









(Zinc-binding dehydrogenases),









Score = −80.6, E-









value = 6.2e−06, N = 1˜cDNA









EST yk164b4.5 comes from this









gene˜cDNA EST









yk164b4.3 comes from this gene˜









cDNA EST yk264f3.5 comes from this


465
2
278
218
1051
g9948219
4.00E−36
conserved hypothetical protein


467
1
142
118
543
g4559318
4.00E−17
BC273239_1


467
1
142
118
543
g186774
9.00E−17
zinc finger protein


467
1
142
118
543
g1017722
9.00E−17
repressor transcriptional factor


468
3
126
78
455
g9963804
5.00E−47
zinc finger protein ZNF286


468
3
126
78
455
g14017965
5.00E−47
KIAA1874 protein


468
3
126
78
455
g5640017
2.00E−46
zinc finger protein ZFP113


469
3
246
228
965
g13676461
1.00E−45
hypothetical protein


469
3
246
228
965
g4589566
1.00E−45
KIAA0961 protein


469
3
246
228
965
g487787
2.00E−37
zinc finger protein ZNF140


470
1
107
40
360
g14348591
2.00E−28
KRAB zinc finger protein


470
1
107
40
360
g7959207
1.00E−27
KIAA1473 protein


470
1
107
40
360
g186774
4.00E−27
zinc finger protein


471
3
357
3
1073
g12052983
1.00E−167
hypothetical protein


471
3
357
3
1073
g14042293
1.00E−135
unnamed protein product


471
3
357
3
1073
g5262560
1.00E−113
hypothetical protein


472
3
90
3
272
g13752754
2.00E−16
zinc flnger 1111


472
3
90
3
272
g14348588
9.00E−15
KRAB zinc finger protein


472
3
90
3
272
g12654015
9.00E−15
Similar to hypothetical protein FLJ10891


473
1
295
1
885
g14495650
1.00E−75
(BC009433) zinc finger protein 331;









zinc finger protein 463


473
1
295
1
885
g8575775
1.00E−75
KRAB zinc finger protein


473
1
295
1
885
g13939858
1.00E−75
RITA


474
1
195
1
585
g7020503
9.00E−68
unnamed protein product


474
1
195
1
585
g8453103
1.00E−67
zinc finger protein


474
1
195
1
585
g8099348
3.00E−67
zinc finger protein


475
2
232
257
952
g14042293
4.00E−53
unnamed protein product


475
2
232
257
952
g14042850
3.00E−47
unnamed protein product


475
2
232
257
952
g12052983
6.00E−38
hypothetical protein


476
2
282
2
847
g10440398
1.00E−93
FLJ00032 protein


476
2
282
2
847
g10047297
1.00E−93
KIAA1611 protein


476
2
282
2
847
g10436789
8.00E−93
unnamed protein product


477
3
149
3
449
g12656631
7.00E−20
Kruppel-like zinc finger protein GLIS2


477
3
149
3
449
g13507039
2.00E−19
Gli-Kruppel zinc-finger protein NKL


477
3
149
3
449
g13507037
2.00E−19
Gli-Kruppel zinc-finger protein NKL


478
3
283
3
851
g13623633
1.00E−174
Unknown (protein for MGC: 13105)


478
3
283
3
851
g488555
3.00E−98
zinc finger protein ZNF135


478
3
283
3
851
g10437767
9.00E−97
unnamed protein product


479
3
264
3
794
g6807587
1.00E−124
hypothetical protein


479
3
264
3
794
g5931821
1.00E−124
dJ228H13.3 (zinc finger protein)


479
3
264
3
794
g488555
1.00E−96
zinc finger protein ZNF135


480
1
201
430
1032
g3540177
1.00E−117
F23269_2


480
1
201
430
1032
g5080758
6.00E−92
BC331191_1


480
1
201
430
1032
g12855931
1.00E−55
putative


481
1
283
880
1728
g14017871
1.00E−143
KIAA1827 protein


481
1
283
880
1728
g10436789
2.00E−97
unnamed protein product


481
1
283
880
1728
g13752754
1.00E−95
zinc finger 1111


482
2
101
131
433
g14042373
1.00E−24
unnamed protein product


482
2
101
131
433
g1389741
7.00E−24
KRAB/zinc finger suppressor protein 1


482
2
101
131
433
g9800824
2.00E−20
bA179N14.1 (novel zinc finger protein)


483
1
101
112
414
g13937999
3.00E−48
Similar to DNA-binding protein


483
1
101
112
414
g3329372
1.00E−34
DNA-binding protein


483
1
101
112
414
g12052732
3.00E−34
hypothetical protein


484
2
297
215
1105
g12862320
2.00E−51
WDC146


486
3
108
462
785
g12856025
1.00E−51
putative


486
3
108
462
785
g12846941
4.00E−37
putative


486
3
108
462
785
g13938537
2.00E−36
Similar to RIKEN cDNA 4933430F16 gene


487
2
122
122
487
g4235144
4.00E−47
BC39498_1


487
2
122
122
487
g4235143
7.00E−34
BC39498_3


487
2
122
122
487
g8163824
4.00E−30
krueppel-like zinc finger protein HZF2


488
1
182
148
693
g12854977
1.00E−41
putative


488
1
182
148
693
g7267246
1.00E−21
putative adenosine deaminase


488
1
182
148
693
g7299138
1.00E−16
CG11994 gene product


489
2
114
293
634
g5262523
3.00E−19
hypothetical protein


489
2
114
293
634
g340170
3.00E−19
orotidine 5′-monophosphate









decarboxylase (EC4.1.1.23)


489
2
114
293
634
g340168
3.00E−19
UMP synthase


490
3
415
3
1247
g2689442
0
R28830_1


490
3
415
3
1247
g1572600
1.00E−172
Zik1


490
3
415
3
1247
g12652759
1.00E−141
hypothetical protein FLJ20557


491
3
43
348
476
g12052884
3.00E−06
hypothetical protein


491
3
43
348
476
g7023332
4.00E−06
unnamed protein product


491
3
43
348
476
g183002
6.00E−05
guanylate binding protein isoform I


492
1
134
49
450
g220637
4.00E−52
zinc finger protein


492
1
134
49
450
g5730196
2.00E−51
Kruppel-type zinc finger


492
1
134
49
450
g14456631
8.00E−51
dJ54B20.4 (novel KRAB box containing









C2H2 type zinc finger protein)


493
3
239
3
719
g14042330
2.00E−96
unnamed protein product


493
3
239
3
719
g10954044
8.00E−92
KRAB zinc finger protein ZFQR


493
3
239
3
719
g10442700
8.00E−92
zinc-finger protein ZBRK1


495
2
185
134
688
g13560888
2.00E−38
EZFIT-related protein 1


495
2
185
134
688
g7243243
2.00E−37
KIAA1431 protein


495
2
185
134
688
g4567178
5.00E−35
R31665_2 (AA 1-673)


496
1
277
178
1008
g4589588
4.00E−67
KIAA0972 protein


496
1
277
178
1008
g498152
4.00E−51
ha0946 protein is Kruppel-related.


496
1
277
178
1008
g6467204
3.00E−38
gonadotropin inducible transcription









repressor-3


497
3
241
3
725
g14043841
3.00E−41
Unknown (protein for MGC: 14429)


497
3
241
3
725
g14042293
6.00E−41
unnamed protein product


497
3
241
3
725
g12052983
2.00E−40
hypothetical protein


498
2
251
1139
1891
g12052983
1.00E−114
hypothetical protein


498
2
251
1139
1891
g5262560
4.00E−68
hypothetical protein


498
2
251
1139
1891
g10434856
1.00E−61
unnamed protein product


499
3
282
54
899
g5080758
1.00E−103
BC331191_1


499
3
282
54
899
g3540177
1.00E−103
F23269_2


499
3
282
54
899
g12855931
1.00E−58
putative


500
1
442
28
1353
g12652727
0
Unknown (protein for IMAGE: 3352566)


500
1
442
28
1353
g488555
1.00E−97
zinc finger protein ZNF135


500
1
442
28
1353
g3378094
1.00E−95
KRAB domain zinc finger protein


501
3
292
3
878
g488551
1.00E−97
zinc finger protein ZNF132


501
3
292
3
878
g13543419
2.00E−97
Similar to zinc finger protein 304


501
3
292
3
878
g1199604
3.00E−97
zinc finger protein C2H2-25


502
1
166
1
498
g12804419
2.00E−65
Unknown (protein for MGC: 1136)


502
1
166
1
498
g12844790
5.00E−64
putative


502
1
166
1
498
g13111895
3.00E−33
Unknown (protein for MGC: 2627)


504
1
406
1
1218
g12053281
0
hypothetical protein


504
1
406
1
1218
g12836135
1.00E−167
putative


504
1
406
1
1218
g3043598
2.00E−64
KIAA0537 protein


505
1
332
1
996
g10438696
1.00E−140
unnamed protein product


505
1
332
1
996
g12847740
7.00E−11
putative


505
1
332
1
996
g7022551
1.00E−09
unnamed protein product


506
2
183
2
550
g4105619
1.00E−94
SPAF


506
2
183
2
550
g12847023
1.00E−94
putative


506
2
183
2
550
g7297973
5.00E−67
CG5776 gene product










[0307]

9








TABLE 8











Parameter


Program
Description
Reference
Threshold







ABIFACTURA
A program that removes vector sequences and
Applied Biosystems, Foster City, CA.




masks ambiguous bases in nucleic acid sequences.


ABI/
A Fast Data Finder useful in comparing and
Applied Biosystems, Foster City, CA;
Mismatch


PARACEL
annotating amino acid or nucleic acid sequences.
Paracel Inc., Pasadena, CA.
<50%


FDF


ABI
A program that assembles nucleic acid sequences.
Applied Biosystems, Foster City, CA.


AutoAssembler


BLAST
A Basic Local Alignment Search Tool useful in
Altschul, S. F. et al. (1990) J. Mol. Biol.
ESTs:



sequence similarity search for amino acid and
215: 403-410; Altschul, S. F. et al. (1997)
Probability



nucleic acid sequences. BLAST includes five
Nucleic Acids Res. 25: 3389-3402.
value = 1.0E−8



functions: blastp, blastn, blastx, tblastn, and tblastx.

or less Full





Length





sequences:





Probability





value =





1.0E−10 or less


FASTA
A Pearson and Lipman algorithm that searches for
Pearson, W. R. and D. J. Lipman (1988) Proc.
ESTs: fasta E



similarity between a query sequence and a group of
Natl. Acad Sci. USA 85: 2444-2448; Pearson,
value =



sequences of the same type. FASTA comprises as
W. R. (1990) Methods Enzymol. 183: 63-98;
1.06E−6



least five functions: fasta, tfasta, fastx, tfastx, and
and Smith, T. F. and M. S. Waterman (1981)
Assembled



ssearch.
Adv. Appl. Math. 2: 482-489.
ESTs: fasta





Identity = 95%





or greater and





Match length =





200 bases or





greater; fastx E





value = 1.0E−8





or less Full





Length





sequences:





fastx score =





100 or greater


BLIMPS
A BLocks IMProved Searcher that matches a
Henikoff, S. and J. G. Henikoff (1991) Nucleic
Probability



sequence against those in BLOCKS, PRINTS,
Acids Res. 19: 6565-6572; Henikoff, J. G. and
value = 1.0E−3



DOMO, PRODOM, and PFAM databases to search
S. Henikoff (1996) Methods Enzymol.
or less



for gene families, sequence homology, and structural
266: 88-105; and Attwood, T. K. et al. (1997) J.



fingerprint regions.
Chem. Inf. Comput. Sci. 37: 417-424.


HMMER
An algorithm for searching a query sequence against
Krogh, A. et al. (1994) J. Mol. Biol.
PEAM hits:



hidden Markov model (HMM)-based databases of
235: 1501-1531; Sonnhammer, E. L. L. et al.
Probability



protein family consensus sequences, such as PFAM.
(1988) Nucleic Acids Res. 26: 320-322;
value = 1.0E−3




Durbin, R. et al. (1998) Our World View, in a
or less




Nutshell, Cambridge Univ. Press, pp. 1-350.
Signal peptide





hits: Score = 0





or greater


ProfileScan
An algorithm that searches for structural and sequence
Gribskov, M. et al. (1988) CABIOS 4: 61-66;
Normalized



motifs in protein sequences that match sequence patterns
Gribskov, M. et al. (1989) Methods Enzymol.
quality score ≧



defined in Prosite.
183: 146-159; Bairoch, A. et al. (1997)
GCG-specified




Nucleic Acids Res. 25: 217-221.
“HIGH” value





for that





particular





Prosite motif.





Generally,





score =





1.4-2.1.


Phred
A base-calling algorithm that examines automated
Ewing, B. et al. (1998) Genome Res.



sequencer traces with high sensitivity and probability.
8: 175-185; Ewing, B. and P. Green




(1998) Genome Res. 8: 186-194.


Phrap
A Phils Revised Assembly Program including SWAT and
Smith, T. F. and M. S. Waterman (1981) Adv.
Score = 120 or



CrossMatch, programs based on efficient implementation
Appl. Math. 2: 482-489; Smith, T.F. and M.S.
greater;



of the Smith-Waterman algorithm, useful in searching
Waterman (1981) J. Mol. Biol. 147: 195-197;
Match length =



sequence homology and assembling DNA sequences.
and Green, P., University of Washington,
56 or greater




Seattle, WA.


Consed
A graphical tool for viewing and editing Phrap assemblies.
Gordon, D. et al. (1998) Genome Res. 8: 195-202.


SPScan
A weight matrix analysis program that scans protein
Nielson, H. et al. (1997) Protein Engineering
Score = 3.5 or



sequences for the presence of secretory signal peptides.
10: 1-6; Claverie, J.M. and S. Audic (1997)
greater




CABIOS 12: 431-439.


TMAP
A program that uses weight matrices to delineate
Persson, B. and P. Argos (1994) J. Mol. Biol.



transmembrane segments on protein sequences and
237: 182-192; Persson, B. and P. Argos (1996)



determine orientation.
Protein Sci. 5: 363-371.


TMHMMER
A program that uses a hidden Markov model (HMM) to
Sonnhammer, E. L. et al. (1998) Proc. Sixth Intl.



delineate transmembrane segments on protein sequences
Conf. on Intelligent Systems for Mol. Biol.,



and determine orientation.
Glasgow et al., eds., The Am. Assoc. for Artificial




Intelligence(AAAI) Press, Menlo Park, CA, and




MIT Press, Cambridge, MA, pp. 175-182.


Motifs
A program that searches amino acid sequences for patterns
Bairoch, A. et al. (1997) Nucleic Acids



that matched those defined in Prosite.
Res. 25: 217-221; Wisconsin Package




Program Manual, version 9, page M51-59, Genetics




Computer Group, Madison, WI.










Claims
  • 1. An isolated polynucleotide selected from the group consisting of: a) a polynucleotide comprising a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-252, b) a polynucleotide comprising a naturally occurring polynucleotide sequence at least 90% identical to a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-252, c) a polynucleotide complementary to the polynucleotide of a), d) a polynucleotide complementary to the polynucleotide of b), and e) an RNA equivalent of a)-d).
  • 2. An isolated polynucleotide of claim 1, selected from the group consisting of SEQ ID NO:1-252.
  • 3. An isolated polynucleotide comprising at least 30 contiguous nucleotides of a polynucleotide of claim 1.
  • 4. An isolated polynucleotide comprising at least 60 contiguous nucleotides of a polynucleotide of claim 1.
  • 5. A composition for the detection of expression of disease detection and treatment polynucleotides comprising at least one of the polynucleotides of claim 1 and a detectable label.
  • 6. A method for detecting a target polynucleotide in a sample, said target polynucleotide having a sequence of a polynucleotide of claim 1, the method comprising: a) amplifying said target polynucleotide or fragment thereof using polymerase chain reaction amplification, and b) detecting the presence or absence of said amplified target polynucleotide or fragment thereof, and, optionally, if present, the amount thereof.
  • 7. A method for detecting a target polynucleotide in a sample, said target polynucleotide having a sequence of a polynucleotide of claim 1, the method comprising: a) hybridize sample with a probe comprising at least contiguous nucleotides comprising a sequence complementary to said target polynucleotide in the sample, and which probe specifically hybridizes to said target polynucleotide, under conditions whereby a hybridization complex is formed between said probe and said target polynucleotide or fragments thereof, and b) detecting the presence or absence of said hybridization complex, and, optionally, if present, the amount thereof.
  • 8. A method of claim 7, wherein the probe comprises at least 30 contiguous nucleotides.
  • 9. A method of claim 7, wherein the probe comprises at least 60 contiguous nucleotides.
  • 10. A recombinant polynucleotide comprising a promoter sequence operably linked to a polynucleotide of claim 1.
  • 11. A cell transformed with a recombinant polynucleotide of claim 10.
  • 12. A transgenic organism comprising a recombinant polynucleotide of claim 10.
  • 13. A method for producing a disease detection and treatment polypeptide encoded by a polynucleotide of claim 1, the method comprising: a) culturing a cell under conditions suitable for expression of the disease detection and treatment polypeptide, wherein said cell is transformed with a recombinant polynucleotide comprising a promoter sequence operably linked to a polynucleotide of claim 1, and b) recovering the disease detection and treatment polypeptide so expressed.
  • 14. A method of claim 13, wherein the polypeptide has an amino acid sequence selected from the group consisting of SEQ ID NO:253-506.
  • 15. An isolated disease detection and treatment polypeptide (MDDT) encoded by at least one of the polynucleotides of claim 2.
  • 16. A method of screening for a test compound that specifically binds to the polypeptide of claim 15, the method comprising: a) combining the polypeptide of claim 15 with at least one compound under suitable conditions, and b) detecting binding of the polypeptide of claim 15 to the test compound, thereby identifying a compound that specifically binds to the polypeptide of claim 15.
  • 17. A microarray wherein at least one element of the microarray is a polynucleotide of claim 3.
  • 18. A method for generating a transcript image of a sample which contains polynucleotides, the method comprising: a) labeling the polynucleotides of the sample, b contacting the elements of the microarray of claim 17 with the labeled polynucleotides of the sample under conditions suitable for the formation of a hybridization complex, and c) quantifying the expression of the polynucleotides in the sample.
  • 19. A method for screening a compound for effectiveness in altering expression of a target polynucleotide, wherein said target polynucleotide comprises a polynucleotide sequence of a polynucleotide of claim 1, the method comprising: a) exposing a sample comprising the target polynucleotide to a compound, under conditions suitable for the expression of the target polynucleotide, b) detecting altered expression of the target polynucleotide, and c) comparing the expression of the target polynucleotide in the presence of varying amounts of the compound and in the absence of the compound.
  • 20. A method for assessing toxicity of a test compound, said method comprising: a) treating a biological sample containing nucleic acids with the test compound, b) hybridizing the nucleic acids of the treated biological sample with a probe comprising at least 20 contiguous nucleotides of a polynucleotide of claim 1 under conditions whereby a specific hybridization complex is formed between said probe and a target polynucleotide in the biological sample, said target polynucleotide comprising a polynucleotide sequence of a polynucleotide of claim 1 or fragment thereof, c) quantifying the amount of hybridization complex, and d) comparing the amount of hybridization complex in the treated biological sample with the amount of hybridization complex in an untreated biological sample, wherein a difference in the amount of hybridization complex in the untreated biological sample is indicative of toxicity of the test compound.
  • 21. An array comprising different nucleotide molecules affixed in distinct physical locations on a solid substrate, wherein at least one of said nucleotide molecules comprises a first oligonucleotide or polynucleotide sequence specifically hybridizable with at least 30 contiguous nucleotides of a target polynucleotide, and wherein said target polynucleotide is a polynucleotide of claim 1.
  • 22. An array of claim 21, wherein said first oligonucleotide or polynucleotide sequence is completely complementary to at least 30 contiguous nucleotides of said target polynucleotide.
  • 23. An array of claim 21, wherein said first oligonucleotide or polynucleotide sequence is completely complementary to at least 60 contiguous nucleotides of said target polynucleotide
  • 24. An array of claim 21, wherein said first oligonucleotide or polynucleotide sequence is completely complementary to said target polynucleotide.
  • 25. An array of claim 21, which is a microarray.
  • 26. An array of claim 21, further comprising said target polynucleotide hybridized to a nucleotide molecule comprising said first oligonucleotide or polynucleotide sequence.
  • 27. An array of claim 21, wherein a linker joins at least one of said nucleotide molecules to said solid substrate.
  • 28. An array of claim 21, wherein each distinct physical location on the substrate contains multiple nucleotide molecules, and the multiple nucleotide molecules at any single distinct physical location have the same sequence, and each distinct physical location on the substrate contains nucleotide molecules having a sequence which differs from the sequence of nucleotide molecules at another distinct physical location on the substrate.
  • 29. An isolated polypeptide selected from the group consisting of: a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:253-506, b) a polypeptide comprising a naturally occurring amino acid sequence at least 90% identical amino acid sequence selected from the g consisting of SEQ ID NO:253-506, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506.
  • 30. An isolated polypeptide of claim 29, having a sequence selected from the group consisting of SEQ ID NO:253-506.
  • 31. An isolated polynucleotide encoding a polypeptide of claim 29.
  • 32. An isolated polynucleotide encoding a polypeptide of claim 30.
  • 33. An isolated polynucleotide of claim 32, having a sequence selected from the group consisting of SEQ ID NO:1-252.
  • 34. An isolated antibody which specifically binds to a disease detection and treatment polypeptide of claim 29.
  • 35. A diagnostic test for a condition or disease associated with the expression of MDDT in a biological sample, the method comprising: a) combining the biological sample with an antibody of claim 34, under conditions suitable for the antibody to bind the polypeptide and form an antibody:polypeptide complex, and b) detecting the complex, wherein the presence of the complex correlates with the presence of the polypeptide in the biological sample.
  • 36. The antibody of claim 34, wherein the antibody is: a) a chimeric antibody, b) a single chain antibody, c) a Fab fragment, d) a F(ab′)2 fragment, or e) a humanized antibody.
  • 37. A composition comprising an antibody of claim 34 and anptable excipient.
  • 38. A method of diagnosing a condition or disease associated with the expression of MDDT in a subject, comprising administering to said subject an effective amount of the composition of claim 37.
  • 39. A composition of claim 37, wherein the antibody is labeled.
  • 40. A method of diagnosing a condition or disease associated with the expression of MDDT in a subject, comprising administering to said subject an effective amount of the composition of claim 39.
  • 41. A method of preparing a polyclonal antibody with the specificity of the antibody of claim 34, the method comprising: a) immunizing an animal with a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506, or an immunogenic fragment thereof, under conditions to elicit an antibody response, b) isolating antibodies from said animal, and c) screening the isolated antibodies with the polypeptide, thereby identifying a polyclonal antibody which binds specifically to a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506.
  • 42. An antibody produced by a method of claim 41.
  • 43. A composition comprising the antibody of claim 42 and a suitable carrier.
  • 44. A method of making a monoclonal antibody with the specificity of the antibody of claim 34, the method comprising: a) immunizing an animal with a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506, or an immunogenic fragment thereof, under conditions to elicit an antibody response, b) isolating antibody producing cells from the animal, c) fusing the antibody producing cells with immortalized cells to form monoclonal antibody-producing hybridoma cells, d) culturing hybridoma cells, and e) isolating from the culture monoclonal antibody which binds specifically to a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506.
  • 45. A monoclonal antibody produced by a method of claim 44.
  • 46. A composition comprising the antibody of claim 45 and a suitable carrier.
  • 47. The antibody of claim 34, wherein the antibody is produced by screening a Fab expression library.
  • 48. The antibody of claim 34, wherein the antibody is produced by screening a recombinant immunoglobulin library.
  • 49. A method of detecting a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506 in a sample, the method comprising: a) incubating the antibody of claim 34 with a sample under conditions to allow specific binding of the antibody and the polypeptide, and b) detecting specific binding, wherein specific binding indicates the presence of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506 in the sample.
  • 50. A method of purifying a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506 from a sample, the method comprising: a) incubating the antibody of claim 34 with a sample under conditions to allow specific binding of the antibody and the polypeptide, and b) separating the antibody from the sample and obtaining the purified polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:253-506.
  • 51. A composition comprising a polypeptide of claim 29 and a pharmaceutically acceptable excipient.
  • 52. A composition of claim 51, wherein the polypeptide has an amino acid sequence of SEQ ID NO:253-506.
  • 53. A method for treating a disease or condition associated with increased expression of functional MDDT, comprising administering to a patient in need of such treatment the composition of claim 51.
  • 54. A method for screening a compound for effectiveness as an agonist of a polypeptide of claim 29, the method comprising: a) exposing a sample comprising a polypeptide of claim 29 to a compound, and b) detecting agonist activity in the sample.
  • 55. A composition comprising an agonist compound identified by a method of claim 54 and a pharmaceutically acceptable excipient.
  • 56. A method for treating a disease or condition associated with decreased expression of functional MDDT, comprising administering to a patient in need of such treatment a composition of claim 55.
  • 57. A method for screening a compound for effectiveness as an antagonist of a polypeptide of claim 29, the method comprising: a) exposing a sample comprising a polypeptide of claim 29 to a compound, and b) detecting antagonist activity in the sample.
  • 58. A composition comprising an antagonist compound identified by a method of claim 57 and a pharmaceutically acceptable excipient.
  • 59. A method for treating a disease or condition associated with overexpression of functional MDDT, comprising administering to a patient in need of such treatment a composition of claim 58.
  • 60. A method of screening for a compound that modulates the activity of the polypeptide of claim 29, said method comprising: a) combining the polypeptide of claim 29 with at least one test compound under conditions permissive for the activity of the polypeptide of claim 29, b) assessing the activity of the polypeptide of claim 29 in the presence of the test compound, and c) comparing the activity of the polypeptide of claim 29 in the presence of the test compound with the activity of the polypeptide of claim 29 in the absence of the test compound wherein a change in the activity of the polypeptide of claim 29 in the presence of the test compound is indicative of a compound that modulates the activity of the polypeptide of claim 29.
PCT Information
Filing Document Filing Date Country Kind
PCT/US01/27628 9/5/2001 WO