Secretory molecules

TECHNICAL FIELD

[0001] The present invention relates to secretory molecules 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 secretory molecules.

BACKGROUND OF THE INVENTION

[0002] Protein transport and secretion are essential for cellular function. Protein transport is mediated by a signal peptide located at the amino terminus of the protein to be transported or secreted. The signal peptide is comprised of about ten to twenty hydrophobic amino acids which target the nascent protein from the ribosome to a particular membrane bound compartment such as the endoplasmic reticulum (ER). Proteins targeted to the ER may either proceed through the secretory pathway or remain in any of the secretory organelles such as the ER, Golgi apparatus, or lysosomes. Proteins that transit through the secretory pathway are either secreted into the extracellular space or retained in the plasma membrane. Proteins that are retained in the plasma membrane contain one or more transmembrane domains, each comprised of about 20 hydrophobic amino acid residues. Proteins that are secreted from the cell are generally synthesized as inactive precursors that are activated by post-translational processing events during transit through the secretory pathway. Such events include glycosylation, proteolysis, and removal of the signal peptide by a signal peptidase. Other events that may occur during protein transport include chaperone-dependent unfolding and folding of the nascent protein and interaction of the protein with a receptor or pore complex. Examples of secretory proteins with amino terminal signal peptides are discussed below and include proteins with important roles in cell-to-cell signaling. Such proteins include transmembrane receptors and cell surface markers, extracellular matrix molecules, cytokines, hormones, growth and differentiation factors, neuropeptides, vasomediators, ion channels, transporters/pumps, and proteases. (Reviewed in Alberts, B. et al. (1994) Molecular Biology of The Cell, Garland Publishing, New York N.Y., pp. 557-560, 582-592.)

[0003] G-protein coupled receptors (GPCRs) comprise a superfamily of integral membrane proteins which transduce extracellular signals. Not all GPCRs contain N-terminal signal peptides. GPCRs include receptors for biogenic amines such as dopamine, epinephrine, histamine, glutamate (metabotropic-type), acetylcholine (muscarinic-type), and serotonin; for lipid mediators of inflammation such as prostaglandins, platelet activating factor, and leukotrienes; for peptide hormones such as calcitonin, C5a anaphylatoxin, follicle stimulating hormone, gonadotropin releasing hormone, neurokinin, oxytocin, and thrombin; and for sensory signal mediators such as retinal photopigments and olfactory stimulatory molecules. The structure of these highly conserved receptors consists of seven hydrophobic transmembrane regions, cysteine disulfide bridges between the second and third extracellular loops, an extracellular N-terminus, and a cytoplasmic C-terminus. The N-terminus interacts with ligands, the disulfide bridges interact with agonists and antagonists, and the large third intracellular loop interacts with G proteins to activate second messengers such as cyclic AMP, phospholipase C, inositol triphosphate, or ion channels. (Reviewed in Watson, S. and Arlinstall, S. (1994) The G-protein Linked Receptor Facts Book, Academic Press, San Diego Calif., pp. 2-6; and Bolander, F. F. (1994) Molecular Endocrinology, Academic Press, San Diego Calif., pp. 162-176.)

[0004] Other types of receptors include cell surface antigens identified on leukocytic cells of the immune system. These antigens have been identified using systematic, monoclonal antibody (mAb)-based “shot gun” techniques. These techniques have resulted in the production of hundreds of mAbs directed against unknown cell surface leukocytic antigens. These antigens have been grouped into “clusters of differentiation” based on common immunocytochemical localization patterns in various differentiated and undifferentiated leukocytic cell types. Antigens in a given cluster are presumed to identify a single cell surface protein and are assigned a “cluster of differentiation” or “CD” designation. Some of the genes encoding proteins identified by CD antigens have been cloned and verified by standard molecular biology techniques. CD antigens have been characterized as both transmembrane proteins and cell surface proteins anchored to the plasma membrane via covalent attachment to fatty acid-containing glycolipids such as glycosylphosphatidylinositol (GPI). (Reviewed in Barclay, A. N. et al. (1995) The Leucocyte Antigen Facts Book, Academic Press, San Diego Calif., pp. 17-20.)

[0005] Matrix proteins (MPs) are transmembrane and extracellular proteins which function in formation, growth, remodeling, and maintenance of tissues and as important mediators and regulators of the inflammatory response. The expression and balance of MPs may be perturbed by biochemical changes that result from congenital, epigenetic, or infectious diseases. In addition, MPs affect leukocyte migration, proliferation, differentiation, and activation in the immune response. MPs are frequently characterized by the presence of one or more domains which may include collagen-like domains, EGF-like domains, immunoglobulin-like domains, and fibronectin-like domains. In addition, MPs may be heavily glycosylated and may contain an Arginine-Glycine-Aspartate (RGD) tripeptide motif which may play a role in adhesive interactions. MPs include extracellular proteins such as fibronectin, collagen, galectin, vitronectin and its proteolytic derivative somatomedin B; and cell adhesion receptors such as cell adhesion molecules (CAMs), cadherins, and integrins. (Reviewed in Ayad, S. et al. (1994) The Extracellular Matrix Facts Book, Academic Press, San Diego Calif., pp. 2-16; Ruoslahti, E. (1997) Kidney Int. 51:1413-1417; Sjaastad, M. D. and Nelson, W. J. (1997) BioEssays 19:47-55.)

[0006] Cytokines are secreted by hematopoietic cells in response to injury or infection. Interleukins, neurotrophins, growth factors, interferons, and chemokines all define cytokine families that work in conjunction with cellular receptors to regulate cell proliferation and differentiation. In addition, cytokines effect activities such as leukocyte migration and function, hematopoietic cell proliferation, temperature regulation, acute response to infection, tissue remodeling, and apoptosis.

[0007] Chemokines, in particular, are small chemoattractant cytokines involved in inflammation, leukocyte proliferation and migration, angiogenesis and angiostasis, regulation of hematopoiesis, HIV infectivity, and stimulation of cytokine secretion. Chemokines generally contain 70-100 amino acids and are subdivided into four subfamilies based on the presence of conserved cysteine-based motifs. (Callard, R. and Gearing, A. (1994) The Cytokine Facts Book, Academic Press, New York N.Y., pp. 181-190, 210-213, 223-227.)

[0008] Growth and differentiation factors are secreted proteins which function in intercellular communication. Some factors require oligomerization or association with MPs for activity. Complex interactions among these factors and their receptors trigger intracellular signal transduction pathways that stimulate or inhibit cell division, cell differentiation, cell signaling, and cell motility. Most growth and differentiation factors act on cells in their local environment (paracrine signaling). There are three broad classes of growth and differentiation factors. The first class includes the large polypeptide growth factors such as epidermal growth factor, fibroblast growth factor, transforming growth factor, insulin-like growth factor, and platelet-derived growth factor. The second class includes the hematopoietic growth factors such as the colony stimulating factors (CSFs). Hematopoietic growth factors stimulate the proliferation and differentiation of blood cells such as B-lymphocytes, T-lymphocytes, erythrocytes, platelets, eosinophils, basophils, neutrophils, macrophages, and their stem cell precursors. The third class includes small peptide factors such as bombesin, vasopressin, oxytocin, endothelin, transferrin, angiotensin II, vasoactive intestinal peptide, and bradykinin which function as hormones to regulate cellular functions other than proliferation.

[0009] Growth and differentiation factors play critical roles in neoplastic transformation of cells in vitro and in tumor progression in vivo. Inappropriate expression of growth factors by tumor cells may contribute to vascularization and metastasis of tumors. During hematopoiesis, growth factor misregulation can result in anemias, leukemias, and lymphomas. Certain growth factors such as interferon are cytotoxic to tumor cells both in vivo and in vitro. Moreover, some growth factors and growth factor receptors are related both structurally and functionally to oncoproteins. In addition, growth factors affect transcriptional regulation of both proto-oncogenes and oncosuppressor genes. (Reviewed in Pimentel, E. (1994) Handbook of Growth Factors, CRC Press, Ann Arbor Mich., pp. 1-9.)

[0010] Proteolytic enzymes or proteases either activate or deactivate proteins by hydrolyzing peptide bonds. Proteases are found in the cytosol, in membrane-bound compartments, and in the extracellular space. The major families are the zinc, serine, cysteine, thiol, and carboxyl proteases.

[0011] Ion channels, ion pumps, and transport proteins mediate the transport of molecules across cellular membranes. Transport can occur by a passive, concentration-dependent mechanism or can be linked to an energy source such as ATP hydrolysis. Symporters and antiporters transport ions and small molecules such as amino acids, glucose, and drugs. Symporters transport molecules and ions unidirectionally, and antiporters transport molecules and ions bidirectionally. Transporter superfamilies include facilitative transporters and active ATP-binding cassette transporters which are involved in multipledrug resistance and the targeting of antigenic peptides to MHC Class I molecules. These transporters bind to a specific ion or other molecule and undergo a conformational change in order to transfer the ion or molecule across the membrane. (Reviewed in Alberts, B. et al. (1994) Molecular Biology of The Cell, Garland Publishing, New York N.Y., pp. 523-546.)

[0012] Ion channels are formed by transmembrane proteins which create a lined passageway across the membrane through which water and ions, such as Na+, K+, Ca2+, and Cl−, enter and exit the cell. For example, chloride channels are involved in the regulation of the membrane electric potential as well as absorption and secretion of ions across the membrane. Chloride channels also regulate the internal pH of membrane-bound organelles.

[0013] Ion pumps are ATPases which actively maintain membrane gradients. Ion pumps are classified as P, V, or F according to their structure and function. All have one or more binding sites for ATP in their cytosolic domains. The P-class ion pumps include Ca2+ ATPase and Na+/K+ ATPase and function in transporting H+, Na+, K+, and Ca2+ ions. P-class pumps consist of two a and two β transmembrane subunits. The V- and F-class ion pumps have similar structures but transport only H+. F class H+ pumps mediate transport across the membranes of mitochondria and chloroplasts, while V-class H+ pumps regulate acidity inside lysosomes, endosomes, and plant vacuoles.

[0014] A family of structurally related intrinsic membrane proteins known as facilitative glucose transporters catalyze the movement of glucose and other selected sugars across the plasma membrane. The proteins in this family contain a highly conserved, large transmembrane domain comprised of 12 α-helices, and several weakly conserved, cytoplasmic and exoplasmic domains. (Pessin, J. E. and Bell, G. I. (1992) Annu. Rev. Physiol. 54:911-930.)

[0015] Amino acid transport is mediated by Na+ dependent amino acid transporters. These transporters are involved in gastrointestinal and renal uptake of dietary and cellular amino acids and in neuronal reuptake of neurotransmitters. Transport of cationic amino acids is mediated by the system y+ family and the cationic amino acid transporter (CAT) family. Members of the CAT family share a high degree of sequence homology, and each contains 12-14 putative transmembrane domains. (Ito, K. and Groudine, M. (1997) J. Biol. Chem. 272:26780-26786.)

[0016] Hormones are secreted molecules that travel through the circulation and bind to specific receptors on the surface of, or within, target cells. Although they have diverse biochemical compositions and mechanisms of action, hormones can be grouped into two categories. One category includes small lipophilic hormones that diffuse through the plasma membrane of target cells, bind to cytosolic or nuclear receptors, and form a complex that alters gene expression. Examples of these molecules include retinoic acid, thyroxine, and the cholesterol-derived steroid hormones such as progesterone, estrogen, testosterone, cortisol, and aldosterone. The second category includes hydrophilic hormones that function by binding to cell surface receptors that transduce signals across the plasma membrane. Examples of such hormones include amino acid derivatives such as catecholamines and peptide hormones such as glucagon, insulin, gastrin, secretin, cholecystokinin, adrenocorticotropic hormone, follicle stimulating hormone, luteinizing hormone, thyroid stimulating hormone, and vasopressin. (See, for example, Lodish et al. (1995) Molecular Cell Biology, Scientific American Books Inc., New York N.Y., pp. 856-864.)

[0017] Neuropeptides and vasomediators (NP/VM) comprise a large family of endogenous signaling molecules. Included in this family are neuropeptides and neuropeptide hormones such as bombesin, neuropeptide Y, neurotensin, neuromedin N, melanocortins, opioids, galanin, somatostatin, tachykinins, urotensin II and related peptides involved in smooth muscle stimulation, vasopressin, vasoactive intestinal peptide, and circulatory system-borne signaling molecules such as angiotensin, complement, calcitonin, endothelins, formyl-methionyl peptides, glucagon, cholecystoknin and gastrin. NP/VMs can transduce signals directly, modulate the activity or release of other neurotransmitters and hormones, and act as catalytic enzymes in cascades. The effects of NP/VMs range from extremely brief to long-lasting. (Reviewed in Martin, C. R. et al. (1985) Endocrine Physiology, Oxford University Press, New York, N.Y., pp. 57-62.)

[0018] The discovery of new secretory molecules 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, cell signaling and the expression of secretory molecules.

SUMMARY OF THE INVENTION

[0019] The present invention relates to nucleic acid sequences comprising human polynucleotides encoding secretory polypeptides that contain signal peptides and/or transmembrane domains. These human polynucleotides (sptm) as presented in the Sequence Listing uniquely identify partial or full length genes encoding structural, functional, and regulatory polypeptides involved in cell signaling.

[0020] 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:1-75; 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:1-75; 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:1-75. 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:1-75; 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:1-75; 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 ED NO:1-75; 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:1-75; 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 secretory 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:1-75; 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:1-75; 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.

[0021] 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:1-75; 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:1-75; 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.

[0022] 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 selected from the group consisting of SEQ ID NO:1-75; 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:1-75; 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 20 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, 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.

[0023] 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:1-75; 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:1-75; 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.

[0024] The invention also provides a method for producing a secretory polypeptide, the method comprising a) culturing a cell under conditions suitable for expression of the secretory 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:1-75; 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:1-75; 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 secretory 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:76-152.

[0025] The invention also provides an isolated secretory polypeptide (SPTM) encoded by at least one polynucleotide comprising a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-75. 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:76-152. The method comprises a) combining the polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:76-152 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:76-152 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:76-152.

[0026] 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:1-75; 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:1-75; 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.

[0027] 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:1-75; 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:1-75; 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.

[0028] 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:1-75; 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:1-75; 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:1-75; 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:1-75; 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.

[0029] 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:76-152, 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:76-152, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:76-152, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:76-152. In one alternative, the invention provides an isolated polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:76-152.

[0030] 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:76-152, 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:76-152, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:76-152, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ D NO:76-152. In one alternative, the polynucleotide encodes a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:76-152. In another alternative, the polynucleotide comprises a polynucleotide sequence selected from the group consisting of SEQ ID NO:1-75.

[0031] 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:76-152, 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:76-152, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:76-152, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:76-152.

[0032] 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:76-152, 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:76-152, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:76-152, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:76-152, 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:76-152. The invention additionally provides a method of treating a disease or condition associated with decreased expression of functional SPTM, comprising administering to a patient in need of such treatment the composition.

[0033] 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:76-152, 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:76-152, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:76-152, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:76-152. 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 SPTM, comprising administering to a patient in need of such treatment the composition.

[0034] 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:76-152, 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:76-152, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:76-152, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:76-152. 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 SPTM, comprising administering to a patient in need of such treatment the composition.

[0035] 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:76-152, 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:76-152, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:76-152, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:76-152. 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

[0036] 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.

[0037] 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 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. For TM domains, the membrane topology of the encoded polypeptide sequence is indicated as being transmembrane or on the cytosolic or non-cytosolic side of the cell membrane or organelle.

[0038] 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 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.

[0039] Table 4 shows the tissue distribution profiles for the templates of the invention.

[0040] Table 5 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.

[0041] Table 6 summarizes the bioinformatics tools which are useful for analysis of the polynucleotides of the present invention. The first column of Table 6 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

[0042] 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 machines, methods, and materials set forth are not intended to limit the scope of the invention which is limited only by the appended claims.

[0043] 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.

[0044] Definitions

[0045] As used herein, the lower case “sptm” refers to a nucleic acid sequence, while the upper case “SPTM” refers to an amino acid sequence encoded by sptm A “full-length” sptm refers to a nucleic acid sequence containing the entire coding region of a gene endogenously expressed in human tissue.

[0046] “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.

[0047] “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 sptm.

[0048] An “allelic variant” is an alternative form of the gene encoding SPTM. Allelic variants may result from at least one mutation in the nucleic acid sequence and may result in altered mRNAs or in polypeptides whose structure or function may or may not be altered. A gene may have none, one, or many allelic variants of its naturally occurring form Common mutational changes which give rise to allelic variants are generally ascribed to natural deletions, additions, or substitutions of nucleotides. Each of these types of changes may occur alone, or in combination with the others, one or more times in a given sequence.

[0049] “Altered” nucleic acid sequences encoding SPTM include those sequences with deletions, insertions, or substitutions of different nucleotides, resulting in a polypeptide the same as SPTM or a polypeptide with at least one functional characteristic of SPTM. Included within this definition are polymorphisms which may or may not be readily detectable using a particular oligonucleotide probe of the polynucleotide encoding SPTM, and improper or unexpected hybridization to allelic variants, with a locus other than the normal chromosomal locus for the polynucleotide sequence encoding SPTM. The encoded protein may also be “altered,” and may contain deletions, insertions, or substitutions of amino acid residues which produce a silent change and result in a functionally equivalent SPTM. Deliberate amino acid substitutions may be made on the basis of similarity in polarity, charge, solubility, hydrophobicity, hydrophilicity, and/or the amphipathic nature of the residues, as long as the biological or immunological activity of SPTM is retained. For example, negatively charged amino acids may include aspartic acid and glutamic acid, and positively charged amino acids may include lysine and arginine. Amino acids with uncharged polar side chains having similar hydrophilicity values may include: asparagine and glutamine; and serine and threonine. Amino acids with uncharged side chains having similar hydrophilicity values may include: leucine, isoleucine, and valine; glycine and alanine; and phenylalanine and tyrosine.

[0050] “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.

[0051] “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.

[0052] “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 SPTM 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 carriers 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.

[0053] The term “aptamer” refers to a nucleic acid or oligonucleotide molecule that binds to a specific molecular target. Aptamers are derived from an in vitro evolutionary process (e.g., SELEX (Systematic Evolution of Ligands by EXponential Enrichment), described in U.S. Pat. No. 5,270,163), which selects for target-specific aptamer sequences from large combinatorial libraries. Aptamer compositions may be double-stranded or single-stranded, and may include deoxyribonucleotides, ribonucleotides, nucleotide derivatives, or other nucleotide-like molecules. The nucleotide components of an aptamer may have modified sugar groups (e.g., the 2′-OH group of a ribonucleotide may be replaced by 2′-F or 2′-NH2), which may improve a desired property, e.g., resistance to nucleases or longer lifetime in blood. Aptamers may be conjugated to other molecules, e.g., a high molecular weight carrier to slow clearance of the aptamer from the circulatory system. Aptamers may be specifically cross-linked to their cognate ligands, e.g., by photo-activation of a cross-linker. (See, e.g., Brody, E. N. and L. Gold (2000) J. Biotechnol. 74:5-13.)

[0054] The term “intramer” refers to an aptamer which is expressed in vivo. For example, a vaccinia virus-based RNA expression system has been used to express specific RNA aptamers at high levels in the cytoplasm of leukocytes (Blind, M. et al. (1999) Proc. Natl. Acad. Sci. USA 96:3606-3610).

[0055] The term “spiegelmer” refers to an aptamer which includes L-DNA, L-RNA, or other left-handed nucleotide derivatives or nucleotide-like molecules. Aptamers containing left-handed nucleotides are resistant to degradation by naturally occurring enzymes, which normally act on substrates containing right-handed nucleotides.

[0056] “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 base.

[0057] “Antisense technology” refers to any technology which relies on the specific hybridization of an antisense sequence to a target sequence.

[0058] 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.

[0059] “Biologically active” refers to an amino acid sequence having a structural, regulatory, or biochemical function of a naturally occurring amino acid sequence.

[0060] “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.

[0061] “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′).

[0062] 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.

[0063] 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).

[0064] “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

[0065] 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.

[0066] “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.

[0067] “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.

[0068] “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.

[0069] The terms “element” and “array element” refer to a polynucleotide, polypeptide, or other chemical compound having a unique and defined position on a microarray.

[0070] The term “modulate” refers to a change in the activity of SPTM. For example, modulation may cause an increase or a decrease in protein activity, binding characteristics, or any other biological, functional, or immunological properties of SPTM.

[0071] “E-value” refers to the statistical probability that a match between two sequences occurred by chance.

[0072] “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.

[0073] A “fragment” is a unique portion of sptm or SPTM which is identical in sequence to but shorter in length than the parent sequence. A fragment may comprise up to 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.

[0074] A fragment of sptm comprises a region of unique polynucleotide sequence that specifically identifies sptm, for example, as distinct from any other sequence in the same genome. A fragment of sptm is useful, for example, in hybridization and amplification technologies and in analogous methods that distinguish sptm from related polynucleotide sequences. The precise length of a fragment of sptm and the region of sptm to which the fragment corresponds are routinely determinable by one of ordinary skill in the art based on the intended purpose for the fragment.

[0075] A fragment of SPTM is encoded by a fragment of sptm. A fragment of SPTM comprises a region of unique amino acid sequence that specifically identifies SPTM. For example, a fragment of SPTM is useful as an immunogenic peptide for the development of antibodies that specifically recognize SPTM. The precise length of a fragment of SPTM and the region of SPTM to which the fragment corresponds are routinely determinable by one of ordinary skill in the art based on the intended purpose for the fragment.

[0076] 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.

[0077] “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.

[0078] “Homology” refers to sequence similarity either between a reference nucleic acid sequence and at least a fragment of an sptm or between a reference amino acid sequence and a fragment of an SPTM.

[0079] “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.

[0080] 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.

[0081] 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.

[0082] 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.

[0083] “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.

[0084] “Immune response” can refer to conditions associated with inflammation, trauma, immune disorders, or infectious or genetic disease, etc. These conditions can be characterized by expression of various factors, e.g., cytokines, chemokines, and other signaling molecules, which may affect cellular and systemic defense systems.

[0085] An “immunogenic fragment” is a polypeptide or oligopeptide fragment of SPTM which is capable of eliciting an immune response when introduced into a living organism, for example, a mammal. The term “immunogenic fragment” also includes any polypeptide or oligopeptide fragment of SPTM which is useful in any of the antibody production methods disclosed herein or known in the art.

[0086] “Insertion” or “addition” refers to a change in either a nucleic or amino acid sequence in which at least one nucleotide or residue, respectively, is added to the sequence.

[0087] “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.

[0088] “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.

[0089] “Linkers” are short stretches of nucleotide sequence which may be added to a vector or an sptm 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).

[0090] “Naturally occurring” refers to an endogenous polynucleotide or polypeptide that may be isolated from viruses or prokaryotic or eukaryotic cells.

[0091] “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.

[0092] “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.

[0093] “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.

[0094] “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.

[0095] 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.

[0096] 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.

[0097] 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. 215:403410), 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.nlm.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:

[0098] Matrix: BLOSUM62

[0099] Reward for match: 1

[0100] Penalty for mismatch: −2

[0101] Open Gap: 5 and Extension Gap: 2 penalties

[0102] Gap×drop-off 50

[0103] Expect: 10

[0104] Word Size: 11

[0105] Filter: on

[0106] 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.

[0107] 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.

[0108] 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.

[0109] 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.

[0110] 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:

[0111] Matrix: BLOSUM62

[0112] Open Gap: 11 and Extension Gap: 1 penalty

[0113] Gap×drop-off: 50

[0114] Expect: 10

[0115] Word Size: 3

[0116] Filter: on

[0117] 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.

[0118] “Post-translational modification” of an SPTM 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 SPTM.

[0119] “Probe” refers to sptm 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).

[0120] 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.

[0121] 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.).

[0122] 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/MIT 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.

[0123] “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.

[0124] 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.

[0125] 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.

[0126] “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.

[0127] “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.

[0128] 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.

[0129] “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).

[0130] “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.

[0131] “Substitution” refers to the replacement of at least one nucleotide or amino acid by a different nucleotide or amino acid.

[0132] “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.

[0133] 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.

[0134] “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.

[0135] “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.

[0136] 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 introduction 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.

[0137] 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.

[0138] 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 SPTM, 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-mediated 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.

[0139] 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.

[0140] The Invention

[0141] 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. Segments of the template sequences are defined by the “start” and “stop” nucleotide positions listed in columns 3 and 4. These segments, when translated in the reading frames indicated in column 5, have similarity to signal peptide (SP) or transmembrane (TM) domain consensus sequences, as indicated in column 6.

[0142] 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 cell signaling. 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.

[0143] Derivation of Nucleic Acid Sequences

[0144] 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.

[0145] 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 lipopolysaccbaride in the case of leukocytic cell lines, or, in the case of endothelial cell lines, subjected to shear stress.

[0146] Sequencing of the cDNAs

[0147] 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.

[0148] 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.)

[0149] Assembly of cDNA Sequences

[0150] 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.

[0151] 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.

[0152] 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.

[0153] 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.

[0154] Analysis of the cDNA Sequences

[0155] 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 6.) 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.

[0156] 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. 215:403410). 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 sptm or SPTM of the present invention.

[0157] 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. Pat. No. 5,953,727; 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.

[0158] 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. Pat. No. 6,023,659, incorporated herein by reference.

[0159] Human Secretory Sequences

[0160] The sptm of the present invention may be used for a variety of diagnostic and therapeutic purposes. For example, an sptm may be used to diagnose a particular condition, disease, or disorder associated with cell signaling. 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; an immune system disorder such as such as inflammation, 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; and a neurological disorder such as epilepsy, ischemic cerebrovascular disease, stroke, cerebral neoplasms, Alzheimer's disease, Pick's disease, Huntington's disease, dementia, Parkinson's disease and other extrapyramidal disorders, amyotrophic lateral sclerosis and other motor neuron disorders, progressive neural muscular atrophy, retinitis pigmentosa, hereditary ataxias, multiple sclerosis and other demyelinating diseases, bacterial and viral meningitis, brain abscess, subdural empyema, epidural abscess, suppurative intracranial thrombophlebitis, myelitis and radiculitis, viral central nervous system disease, prion diseases including kuru, Creutzfeldt-Jakob disease, and Gerstmann-Straussler-Scheinker syndrome, fatal familial insomnia, nutritional and metabolic diseases of the nervous system, neurofibromatosis, tuberous sclerosis, cerebelloretinal hemangioblastomatosis, encephalotrigeminal syndrome, mental retardation and other developmental disorder of the central nervous system, cerebral palsy, a neuroskeletal disorder, an autonomic nervous system disorder, a cranial nerve disorder, a spinal cord disease, muscular dystrophy and other neuromuscular disorder, a peripheral nervous system disorder, dermatomyositis and polymyositis, inherited, metabolic, endocrine, and toxic myopathy, myasthenia gravis, periodic paralysis, a mental disorder including mood, anxiety, and schizophrenic disorder, seasonal affective disorder (SAD), akathesia, amnesia, catatonia, diabetic neuropathy, tardive dyskinesia, dystonias, paranoid psychoses, postherpetic neuralgia, and Tourette's disorder. The sptm can be used to detect the presence of, or to quantify the amount of, an sptm-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 sptm can inhibit or inactivate a therapeutically relevant gene related to the sptm.

[0161] Analysis of sptm Expression Patterns

[0162] The expression of sptm may be routinely assessed by hybridization-based methods to determine, for example, the tissue-specificity, disease-specificity, or developmental stage-specificity of sptm expression. For example, the level of expression of sptm may be compared 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 sptm expression in fully or partially differentiated cells or tissues, to determine if changes in sptm 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 sptm 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.

[0163] Hybridization and Genetic Analysis

[0164] The sptm, 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 sptm 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 sptm allows for the detection of nucleic acid sequences, including genomic sequences, which are identical or related to the sptm 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:1-75 and tested for their ability to identify or amplify the target nucleic acid sequence using standard protocols.

[0165] Polynucleotide sequences that are capable of hybridizing, in particular, to those shown in SEQ ID NO:1-75 and fragments thereof, can be identified using various conditions of stringency. (See, e.g., Wahl, G. M. and S. L. Berger (1987) Methods Enzymol. 152:399407; Kimmel, A. R. (1987) Methods Enzymol. 152:507-511.) Hybridization conditions are discussed in “Definitions.”

[0166] A probe for use in Southern or northern hybridization may be derived from a fragment of an sptm 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 sptm. 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 sptm and may be produced by hand or by using available devices, materials, and machines.

[0167] Microarrays may be prepared, used, and analyzed using methods known 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.)

[0168] 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, sptm 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).

[0169] Additionally the polynucleotides of SEQ ID NO:1-75 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 sptm in order to analyze, e.g., regulatory elements.

[0170] Genetic Mapping

[0171] 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.

[0172] 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, Lander, E. 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.

[0173] In another embodiment of the invention, sptm sequences may be used to generate hybridization probes useful in chromosomal mapping of naturally occurring genomic sequences. Either coding or noncoding sequences of sptm may be used, and in some instances, noncoding sequences may be preferable over coding sequences. For example, conservation of an sptm 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.)

[0174] 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 sptm 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 sptm sequences may also be used to detect polymorphisms that are genetically linked to the inheritance of a particular condition, disease, or disorder.

[0175] 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.

[0176] Once a disease-associated gene is mapped to a chromosomal region, the gene must be cloned in order to identify mutations or other alterations (e.g., translocations or inversions) 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.

[0177] Diagnostic Uses

[0178] The sptm 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 sptm expression. Labeled probes developed from sptm sequences are added to a sample under hybridizing conditions of desired stringency. In some instances, sptm, or fragments or oligonucleotides derived from sptm, 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 sptm 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.

[0179] The probes described above may also be used to monitor the progress of conditions, disorders, or diseases associated with abnormal levels of sptm expression, or to evaluate the efficacy of a particular therapeutic treatment. The candidate probe may be identified from the sptm 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.

[0180] 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.

[0181] In a particular aspect, oligonucleotide primers derived from the sptm 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 sptm 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.).

[0182] 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.

[0183] 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 contamination.

[0184] 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.

[0185] Disease Model Systems Using sptm

[0186] The polynucleotides encoding SPTM 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 (Marti, 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.

[0187] The polynucleotides encoding SPTM 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).

[0188] The polynucleotides encoding SPTM 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 sptm 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 sptm, resulting, e.g., in the secretion of SPTM in its milk, may also serve as a convenient source of that protein (Janne, J. et al. (1998) Biotechnol. Annu. Rev. 4:55-74).

[0189] Screening Assays

[0190] SPTM 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.

[0191] 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.

[0192] 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.

[0193] 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.

[0194] 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.

[0195] 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.

[0196] Transcript Imaging and Toxicological Testing

[0197] Another embodiment relates to the use of sptm 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 cell signaling.

[0198] Transcript images which profile sptm expression may be generated using transcripts isolated from tissues, cell lines, biopsies, or other biological samples. The transcript image may thus reflect sptm expression in vivo, as in the case of a tissue or biopsy sample, or in vitro, as in the case of a cell line.

[0199] Transcript images which profile sptm 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.

[0200] In one embodiment, the toxicity of a test compound is assessed by 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.

[0201] Another particular embodiment relates to the use of SPTM 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.

[0202] A proteomic profile may also be generated using antibodies specific for SPTM to quantify the levels of SPTM 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 (Lueling, 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.

[0203] 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.

[0204] 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 SPTM encoded by polynucleotides of the present invention.

[0205] 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 SPTM 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.

[0206] Transcript images may be used to profile sptm expression in distinct tissue types. This process can be used to determine cell signaling 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 sptm 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 cell signaling activity.

[0207] Transcript images of cell lines can be used to assess cell signaling 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 cell signaling activity. Candidate pharmaceutical agents may be evaluated by comparing their associated transcript images with those of pharmaceutical agents of known effectiveness.

[0208] Antisense Molecules

[0209] 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.

[0210] The polynucleotides of the present invention and fragments thereof can be used as antisense sequences to modify the expression of the polypeptide encoded by sptm. 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.)

[0211] 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, J. J. (1995) Br. Med. Bull. 51(1):217-225; Boado, R. 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.)

[0212] Expression

[0213] In order to express a biologically active SPTM, the nucleotide sequences encoding SPTM 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 SPTM 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.)

[0214] A variety of expression vector/host systems may be utilized to contain and express sequences encoding SPTM. 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.

[0215] For long term production of recombinant proteins in mammalian systems, stable expression of SPTM in cell lines is preferred. For example, sequences encoding SPTM can be transformed into cell lines using expression vectors which may contain viral origins of replication 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.)

[0216] Therapeutic Uses of sptm

[0217] The polynucleotides encoding SPTM 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 270:475480; Bordignon, C. et al. (1995) Science 270:470475), 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 sptm expression or regulation causes disease, the expression of sptm from an appropriate population of transduced cells may alleviate the clinical manifestations caused by the genetic deficiency.

[0218] In a further embodiment of the invention, diseases or disorders caused by deficiencies in sptm are treated by constructing mammalian expression vectors comprising sptm and introducing these vectors by mechanical means into sptm-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).

[0219] Expression vectors that may be effective for the expression of sptm 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 sptm 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. 9:451456), 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 SPTM from a normal individual.

[0220] 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.

[0221] In another embodiment of the invention, diseases or disorders caused by genetic defects with respect to sptm expression are treated by constructing a retrovirus vector consisting of (i) sptm 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 cells 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).

[0222] In the alternative, an adenovirus-based gene therapy delivery system is used to deliver sptm to cells which have one or more genetic abnormalities with respect to the expression of sptm. 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.

[0223] In another alternative, a herpes-based, gene therapy delivery system is used to deliver sptm to target cells which have one or more genetic abnormalities with respect to the expression of sptm. The use of herpes simplex virus (HSV)-based vectors may be especially valuable for introducing sptm 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.

[0224] In another alternative, an alphavirus (positive, single-stranded RNA virus) vector is used to deliver sptm 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) Curr. Opin. 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 sptm into the alphavirus genome in place of the capsid-coding region results in the production of a large number of sptm RNAs and the synthesis of high levels of SPTM 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 sptm 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.

[0225] Antibodies

[0226] Anti-SPTM 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.

[0227] The amino acid sequence encoded by the sptm 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 limpet hemocyanin (KLH; Sigma, St. Louis Mo.) for antibody production. A peptide encompassing an antigenic region may be expressed from an sptm, synthesized as described above, or purified from human cells.

[0228] 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 a peptide. Depending on the host species, various adjuvants may be used to increase immunological response.

[0229] In one procedure, peptides about 15 residues in length may be synthesized using an ABI 431A 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-SPTM activity using protocols well known in the art, including ELISA, radioimmunoassay (RIA), and immunoblotting.

[0230] 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.

[0231] 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-SPTM activity using protocols well known in the art, including ELISA, RIA, and immunoblotting.

[0232] 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 sptm can be used to purify and characterize full-length SPTM protein and its activity, binding partners, etc.

[0233] Assays Using Antibodies

[0234] Anti-SPTM antibodies may be used in assays to quantify the amount of SPTM 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.

[0235] 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 SPTM and its specific antibody and the measurement of such complexes. These and other assays are described in Pound (supra).

[0236] 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.

[0237] 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.

[0238] The disclosures of all patents, applications, and publications mentioned above and below, including U.S. Ser. No. 60/261,865, U.S. Ser. No. 60/262,599, U.S. Ser. No. 60/263,329, U.S. Ser. No. 60/262,209, U.S. Ser. No. 60/263,131, U.S. Ser. No. 60/262,208, U.S. Ser. No. 60/262,164, U.S. Ser. No. 60/263,063, U.S. Ser. No. 60/261,864, U.S. Ser. No. 60/262,760, U.S. Ser. No. 60/261,981, U.S. Ser. No. 60/263,070, U.S. Ser. No. 60/261,979, U.S. Ser. No. 60/263,066, U.S. Ser. No. 60/263,077, U.S. Ser. No. 60/263,076, U.S. Ser. No. 60/263,074, and U.S. Ser. No. 60/263,069, are hereby expressly incorporated by reference.

EXAMPLES

[0239] I. Construction of cDNA Libraries

[0240] 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.

[0241] 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 paramagnetic particles (Promega Corporation (Promega), 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.).

[0242] 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), PCR2-TOPOTA plasmid (Invitrogen), PCMV-ICIS plasmid (Stratagene), pIGEN (Incyte Genomics, Palo Alto Calif.), pRARE (Incyte Genomics), or pINCY (Incyte Genomics), 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.

[0243] II. Isolation of cDNA Clones

[0244] Plasmids were recovered from host cells by in vivo excision using the UNZAP 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.

[0245] 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).

[0246] III. Sequencing and Analysis

[0247] 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.

[0248] IV. Assembly and Analysis of Sequences

[0249] 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 preprocessing 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.

[0250] 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 3 along with their positions along the template nucleotide sequences.

[0251] 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.

[0252] 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.

[0253] The final assembled templates were subsequently annotated using the following procedure. Template sequences were analyzed using BLASTN (v2.0, NCBI) versus gbpri (GenBank version 126). “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 126). (See Table 6). 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.

[0254] 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. Pat. No. 6,023,659; “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. Pat. No. 5,953,727; 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.

[0255] 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.). (See also World Wide Web site http://pfam.wustl.edu/ for detailed descriptions of Pfam protein domains and families.)

[0256] 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 T a program that uses a hidden Markov model (HMM) to delineate transmembrane segments on protein sequences and determine orientation (Sonnhammer, E. L. et al. (1998) Proc. Sixth Intl. Conf. On Intelligent Systems for Mol. Biol., Glasgow et al., eds., The Am. Assoc. for Artificial Intelligence (AAAI) Press, Menlo Park, Calif., and MIT Press, Cambridge, Mass., pp. 175-182.) Regions of templates which, when translated, contain similarity to signal peptide or transmembrane consensus sequences are reported in Table 2.

[0257] Template sequences are further analyzed using the bioinformatics tools listed in Table 6, 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.

[0258] The template sequences were translated to derive the corresponding longest open reading frame as presented by the polypeptide sequences as reported in Table 5. 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 126)). 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.

[0259] Table 5 shows sequences with homology to the polypeptides of the invention as identified by BLAST analysis against the 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.

[0260] V. Analysis of Polynucleotide Expression

[0261] 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.)

[0262] 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:

\frac{BLAST Score \times Percent Identity}{5 \times minimum {length (Seq . 1), length (Seq . 2)}}

[0263] 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 of 50 is produced either by 100% identity and 50% overlap at one end, or 79% identity and 100% overlap.

[0264] Alternatively, polynucleotide sequences encoding SPTM are analyzed with respect to the tissue sources from which they were derived. Polynucleotide sequences encoding SPTM were assembled, at least in part, with overlapping Incyte cDNA sequences. Each cDNA sequence is derived from a cDNA library constructed from a human tissue. Each human tissue is classified into one of the following organ/tissue 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. The number of libraries in each category for each polynucleotide sequence encoding SPTM is counted and divided by the total number of libraries across all categories for each polynucleotide sequence encoding SPTM. Similarly, each human tissue is classified into one of the following disease/condition categories: cancer, cell line, developmental, inflammation, neurological, trauma, cardiovascular, pooled, and other, and the number of libraries in each category for each polynucleotide sequence encoding SPTM is counted and divided by the total number of libraries across all categories for each polynucleotide sequence encoding SPTM. The resulting percentages reflect the tissue-specific and disease-specific expression of cDNA encoding SPTM. Percentage values of tissue-specific expression are reported in. cDNA sequences and cDNA library/tissue information are found in the LIFESEQ GOLD database (Incyte Genomics, Palo Alto Calif.).

[0265] VI. Tissue Distribution Profiling

[0266] 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 LIFESQ GOLD database (Incyte Genomics, Palo Alto Calif.).

[0267] Table 4 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.

[0268] VII. Transcript Image Analysis

[0269] 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.

[0270] VIII. Extension of Polynucleotide Sequences and Isolation of a Full-Length cDNA

[0271] Oligonucleotide primers designed using an sptm 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.

[0272] 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, 200 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.

[0273] 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.

[0274] 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.

[0275] 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).

[0276] In like manner, the sptm is used to obtain regulatory sequences (promoters, introns, and enhancers) using the procedure above, oligonucleotides designed for such extension, and an appropriate genomic library.

[0277] IX. Labeling of Probes and Southern Hybridization Analyses

[0278] Hybridization probes derived from the sptm 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-All 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.

[0279] 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.

[0280] X. Chromosome Mapping of sptm

[0281] The cDNA sequences which were used to assemble SEQ ID NO:1-75 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:1-75 are assembled into clusters of contiguous and overlapping sequences using assembly algorithms such as PHRAP (Table 6). 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:1-75 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-arm (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.

[0282] XI. Microarray Analysis

[0283] Probe Preparation from Tissue or Cell Samples

[0284] 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.

[0285] Microarray Preparation

[0286] 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).

[0287] 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.

[0288] 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.

[0289] Microarrays are V-crosslinked using a STRATALNKER 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.

[0290] Hybridization

[0291] 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.

[0292] Detection

[0293] 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.

[0294] 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.

[0295] 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.

[0296] 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.

[0297] 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).

[0298] XII. Complementary Nucleic Acids

[0299] Sequences complementary to the sptm 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 sptm 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.

[0300] XIII. Expression of SPTM

[0301] Expression and purification of SPTM is accomplished using bacterial or virus-based expression systems. For expression of SPTM in bacteria, DNA encoding SPTM 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 SPTM upon induction with isopropyl beta-D-thiogalactopyranoside (IPTG). Expression of SPTM 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 SPTM 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.)

[0302] In most expression systems, SPTM 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 SPTM 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 SPTM obtained by these methods can be used directly in the following activity assay.

[0303] XIV. Demonstration of SPTM Activity

[0304] An assay for SPTM activity measures the expression of SPTM on the cell surface. cDNA encoding SPTM is subcloned into an appropriate mammalian expression vector suitable for high levels of cDNA expression. The resulting construct is transfected into a nonhuman cell line such as NIH3T3. Cell surface proteins are labeled with biotin using methods known in the art. Immunoprecipitations are performed using SPTM-specific antibodies, and immunoprecipitated samples are analyzed using SDS-PAGE and immunoblotting techniques. The ratio of labeled immunoprecipitant to unlabeled immunoprecipitant is proportional to the amount of SPTM expressed on the cell surface.

[0305] Alternatively, an assay for SPTM activity measures the amount of SPTM in secretory, membrane-bound organelles. Transfected cells as described above are harvested and lysed. The lysate is fractionated using methods known to those of skill in the art, for example, sucrose gradient ultracentrifugation. Such methods allow the isolation of subcellular components such as the Golgi apparatus, ER, small membrane-bound vesicles, and other secretory organelles. Immunoprecipitations from fractionated and total cell lysates are performed using SPTM-specific antibodies, and immunoprecipitated samples are analyzed using SDS-PAGE and immunoblotting techniques. The concentration of SPTM in secretory organelles relative to SPTM in total cell lysate is proportional to the amount of SPTM in transit through the secretory pathway.

[0306] XV. Functional Assays

[0307] SPTM function is assessed by expressing sptm 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.

[0308] 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.

[0309] 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.

[0310] The influence of SPTM on gene expression can be assessed using highly purified populations of cells transfected with sequences encoding SPTM and either CD64 or CD64-GFP. CD64 and CD64-GFP are expressed on the surface of transfected cells and bind to conserved 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 SPTM and other genes of interest can be analyzed by northern analysis or microarray techniques.

[0311] XVI. Production of Antibodies

[0312] SPTM substantially purified using polyacrylamide gel electrophoresis (PAGE; see, e.g., Harrington, M. G. (1990) Methods Enzymol. 182:488495), or other purification techniques, is used to immunize rabbits and to produce antibodies using standard protocols.

[0313] Alternatively, the SPTM 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.)

[0314] 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 radioiodinated goat anti-rabbit IgG. Antisera with antipeptide activity are tested for anti-SPTM activity using protocols well known in the art, including ELISA, RIA, and immunoblotting.

[0315] XVII. Purification of Naturally Occurring SPTM Using Specific Antibodies

[0316] Naturally occurring or recombinant SPTM is substantially purified by immunoaffinity chromatography using antibodies specific for SPTM. An immunoaffinity column is constructed by covalently coupling anti-SPTM 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.

[0317] Media containing SPTM are passed over the immunoaffinity column, and the column is washed under conditions that allow the preferential absorbance of SPTM (e.g., high ionic strength buffers in the presence of detergent). The column is eluted under conditions that disrupt antibody/SPTM binding (e.g., a buffer of pH 2 to pH 3, or a high concentration of a chaotrope, such as urea or thiocyanate ion), and SPTM is collected.

[0318] XVIII. Identification of Molecules Which Interact with SPTM

[0319] SPTM, or biologically active fragments thereof, are labeled with 125I 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 SPTM, washed, and any wells with labeled SPTM complex are assayed. Data obtained using different concentrations of SPTM are used to calculate values for the number, affinity, and association of SPTM with the candidate molecules.

[0320] Alternatively, molecules interacting with SPTM 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).

[0321] SPTM 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).

[0322] 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 ID1LI:418914.1:2001JAN1276LI:418914.1.orf1:2001JAN122LI:246108.7:2001JAN1277LI:246108.7.orf3:2001JAN123LI:204262.2:2001JAN1278LI:204262.2.orf1:2001JAN124LI:331661.1:2001JAN1279LI:331661.1.orf1:2001JAN125LI:335074.1:2001JAN1280LI:335074.1.orf1:2001JAN126LI:154608.1:2001JAN1281LI:154608.1.orf2:2001JAN127LI:462889.1:2001JAN1282LI:462889.1.orf2:2001JAN128LI:236680.2:2001JAN1283LI:236680.2.orf2:2001JAN129LI:228186.1:2001JAN1284LI:228186.1.orf2:2001JAN1210LI:721233.1:2001JAN1285LI:721233.1.orf1:2001JAN1211LI:291759.2:2001JAN1286LI:291759.2.orf2:2001JAN1212LI:292613.17:2001JAN1287LI:292613.17.orf1:2001JAN1213LI:412959.15:2001JAN1288LI:412959.15.orf3:2001JAN1214LI:482512.3:2001JAN1289LI:482512.3.orf1:2001JAN1214LI:482512.3:2001JAN1290LI:482512.3.orf2:2001JAN1215LI:413231.6:2001JAN1291LI:413231.6.orf1:2001JAN1216LI:203383.1:2001JAN1292LI:203383.1.orf1:2001JAN1217LI:133186.4:2001JAN1293LI:133186.4.orf3:2001JAN1218LI:238576.2:2001JAN1294LI:238576.2.orf1:2001JAN1219LI:903914.3:2001JAN1295LI:903914.3.orf2:2001JAN1220LI:150817.1:2001JAN1296LI:150817.1.orf2:2001JAN1221LI:219627.1:2001JAN1297LI:219627.1.orf3:2001JAN1222LI:197812.4:2001JAN1298LI:197812.4.orf3:2001JAN1223LI:101525.1:2001JAN1299LI:101525.1.orf2:2001JAN1224LI:891123.1:2001JAN12100LI:891123.1.orf3:2001JAN1225LI:813500.1:2001JAN12101LI:813500.1.orf1:2001JAN1226LI:1037251.1:2001JAN12102LI:1037251.1.orf1:2001JAN1227LI:2032187.1:2001JAN12103LI:2032187.1.orf2:2001JAN1228LI:347572.1:2001JAN12104LI:347572.1.orf3:2001JAN1229LI:007788.1:2001JAN12105LI:007788.1.orf1:2001JAN1230LI:336872.1:2001JAN12106LI:336872.1.orf2:2001JAN1230LI:336872.1:2001JAN12107LI:336872.1.orf3:2001JAN1231LI:1143291.1:2001JAN12108LI:1143291.1.orf2:2001JAN1232LI:093477.1:2001JAN12109LI:093477.1.orf1:2001JAN1233LI:222105.1:2001JAN12110LI:222105.1.orf2:2001JAN1234LI:816737.2:2001JAN12111LI:816737.2.orf3:2001JAN1235LI:475524.1:2001JAN12112LI:475524.1.orf2:2001JAN1236LI:383639.1:2001JAN12113LI:383639.1.orf1:2001JAN1237LI:814346.1:2001JAN12114LI:814346.1.orf2:2001JAN1238LI:898195.6:2001JAN12115LI:898195.6.orf2:2001JAN1239LI:210497.2:2001JAN12116LI:210497.2.orf3:2001JAN1240LI:110297.4:2001JAN12117LI:110297.4.orf2:2001JAN1241LI:2051312.1:2001JAN12118LI:2051312.1.orfl:2001JAN1242LI:350272.2:2001JAN12119LI:350272.2.orf3:2001JAN1243LI:1085472.4:2001JAN12120LI:1085472.4.ort1:2001JAN1244LI:1190272.1:2001JAN12121LI:1190272.1.orf2:2001JAN1245LI:1086797.1:2001JAN12122LI:1086797.1.orf1:2001JAN1246LI:1144466.1:2001JAN12123LI:1144466.1.orf1:2001JAN1247LI:1147914.1:2001JAN12124LI:1147914.1.orf3:2001JAN1248LI:758086.1:2001JAN12125LI:758086.1.orf2:2001JAN1249LI:765245.5:2001JAN12126LI:765245.5.orf3:2001JAN1250LI:335608.2:2001JAN12127LI:335608.2.orf3:2001JAN1251LI:405795.1:2001JAN12128LI:405795.1.orf3:2001JAN1262LI:014872.1:2001JAN12129LI:014872.1.orf3:2001JAN1253LI:239245,3:2001JAN12130LI:239245.3,orf3:2001JAN1254LI:142384.5:2001JAN12131LI:142384.5.orf3:2001JAN1255LI:2068768.1:2001JAN12132LI:2068768.1.orf3:2001JAN1266LI:2118074.1:2001JAN12133LI:2118074.1.orf3:2001JAN1257LI:1189068.4:2001JAN12134LI:1189068.4.orf2:2001JAN1258LI:2118704.1:2001JAN12135LI:2118704.1.orfl:2001JAN1259LI:03 1700.2:2001JAN12136LI:031700.2.orf3:2001JAN1260LI:2120122.1:2001JAN12137LI:2120122.1.orf1:2001JAN1261LI:816174.1:2001JAN12138LI:816174.1.orf1:2001JAN1262LI:1189569.11:2001JAN12139LI:1189569.11.orf2:2001JAN1263LI:413584.1:2001JAN12140LI:413584.1.orf1:2001JAN1264LI:791042.1:2001JAN12141LI:791042.1.orf2:2001JAN1265LI:1167140.1:2001JAN12142LI:1167140.1.orf3:2001JAN1266LI:054831.1:2001JAN12143LI:054831.1.orf2:2001JAN1267LI:1175083.1:2001JAN12144LI:1175083.1.orf2:2001JAN1268LI:2122897.2:2001JAN12145LI:2122897.2.orf2:2001JAN1269LI:2053195.3:2001JAN12146LI:2053195.3.orf3:2001JAN1270LI:439397.6:2001JAN12147LI:439397.6.orf2:2001JAN1271LI:816379.6:2001JAN12148LI:816379.6.orf2:2001JAN1272LI:2123452.4:2001JAN12149LI:2123452.4.orf3:2001JAN1273LI:474559.8:2001JAN12150LI:474559.8.orf3:2001JAN1274LI:1089871.1:2001JAN12151LI:1089871.1.orf3:2001JAN1275LI:289608.1:2001JAN12152LI:289608.1.orf3:2001JAN12

[0323]

3

TABLE 2

SEQ ID NO:
Template ID
Start
Stop
Frame
Domain Type
Topology

1
LI:418914.1:2001JAN12
1
120
forward 1
TM
Cytosolic

1
LI:418914.1:2001JAN12
121
143
forward 1
TM
Transmembrane

1
LI:418914.1:2001JAN12
144
482
forward 1
TM
Non-cytosolic

1
LI:418914.1:2001JAN12
483
505
forward 1
TM
Transmembrane

1
LI:418914.1:2001JAN12
506
508
forward 1
TM
Cytosolic

1
LI:418914.1:2001JAN12
1
115
forward 3
TM
Cytosolic

1
LI:418914.1:2001JAN12
116
138
forward 3
TM
Transmembrane

1
LI:418914.1:2001JAN12
139
142
forward 3
TM
Non-cytosolic

1
LI:418914.1:2001JAN12
143
165
forward 3
TM
Transmembrane

1
LI:418914.1:2001JAN12
166
322
forward 3
TM
Cytosolic

1
LI:418914.1:2001JAN12
323
345
forward 3
TM
Transmembrane

1
LI:418914.1:2001JAN12
346
359
forward 3
TM
Non-cytosolic

1
LI:418914.1:2001JAN12
360
382
forward 3
TM
Transmembrane

1
LI:418914.1:2001JAN12
383
388
forward 3
TM
Cytosolic

1
LI:418914.1:2001JAN12
389
406
forward 3
TM
Transmembrane

1
LI:418914.1:2001JAN12
407
420
forward 3
TM
Non-cytosolic

1
LI:418914.1:2001JAN12
421
443
forward 3
TM
Transmembrane

1
LI:418914.1:2001JAN12
444
507
forward 3
TM
Cytosolic

2
LI:246108.7:2001JAN12
1
41
forward 1
TM
Cytosolic

2
LI:246108.7:2001JAN12
42
59
forward 1
TM
Transmembrane

2
LI:246108.7:2001JAN12
60
109
forward 1
TM
Non-cytosolic

2
LI:246108.7:2001JAN12
110
132
forward 1
TM
Transmembrane

2
LI:246108.7:2001JAN12
133
143
forward 1
TM
Cytosolic

2
LI:246108.7:2001JAN12
144
166
forward 1
TM
Transmembrane

2
LI:246108.7:2001JAN12
167
175
forward 1
TM
Non-cytosolic

2
LI:246108.7:2001JAN12
176
198
forward 1
TM
Transmembrane

2
LI:246108.7:2001JAN12
199
210
forward 1
TM
Cytosolic

2
LI:246108.7:2001JAN12
211
233
forward 1
TM
Transmembrane

2
LI:246108.7:2001JAN12
234
249
forward 1
TM
Non-cytosolic

2
LI:246108.7:2001JAN12
1
19
forward 2
TM
Cytosolic

2
LI:246108.7:2001JAN12
20
42
forward 2
TM
Transmembrane

2
LI:246108.7:2001JAN12
43
56
forward 2
TM
Non-cytosolic

2
LI:246108.7:2001JAN12
57
74
forward 2
TM
Transmembrane

2
LI:246108.7:2001JAN12
75
86
forward 2
TM
Cytosolic

2
LI:246108.7:2001JAN12
87
104
forward 2
TM
Transmembrane

2
LI:246108.7:2001JAN12
105
113
forward 2
TM
Non-cytosolic

2
LI:246108.7:2001JAN12
114
136
forward 2
TM
Transmembrane

2
LI:246108.7:2001JAN12
137
142
forward 2
TM
Cytosolic

2
LI:246108.7:2001JAN12
143
165
forward 2
TM
Transmembrane

2
LI:246108.7:2001JAN12
166
184
forward 2
TM
Non-cytosolic

2
LI:246108.7:2001JAN12
185
207
forward 2
TM
Transmembrane

2
LI:246108.7:2001JAN12
208
249
forward 2
TM
Cytosolic

2
LI:246108.7:2001JAN12
1
79
forward 3
TM
Cytosolic

2
LI:246108.7:2001JAN12
80
102
forward 3
TM
Transmembrane

2
LI:246108.7:2001JAN12
103
111
forward 3
TM
Non-cytosolic

2
LI:246108.7:2001JAN12
112
131
forward 3
TM
Transmembrane

2
LI:246108.7:2001JAN12
132
135
forward 3
TM
Cytosolic

2
LI:246108.7:2001JAN12
136
158
forward 3
TM
Transmembrane

2
LI:246108.7:2001JAN12
159
248
forward 3
TM
Non-cytosolic

3
LI:204262.2:2001JAN12
1
144
forward 1
TM
Cytosolic

3
LI:204262.2:2001JAN12
145
167
forward 1
TM
Transmembrane

3
LI:204262.2:2001JAN12
168
220
forward 1
TM
Non-cytosolic

3
LI:204262.2:2001JAN12
221
243
forward 1
TM
Transmembrane

3
LI:204262.2:2001JAN12
244
374
forward 1
TM
Cytosolic

3
LI:204262.2:2001JAN12
1
154
forward 2
TM
Cytosolic

3
LI:204262.2:2001JAN12
155
177
forward 2
TM
Transmembrane

3
LI:204262.2:2001JAN12
178
207
forward 2
TM
Non-cytosolic

3
LI:204262.2:2001JAN12
208
230
forward 2
TM
Transmembrane

3
LI:204262.2:2001JAN12
231
241
forward 2
TM
Cytosolic

3
LI:204262.2:2001JAN12
242
264
forward 2
TM
Transmembrane

3
LI:204262.2:2001JAN12
265
312
forward 2
TM
Non-cytosolic

3
LI:204262.2:2001JAN12
313
332
forward 2
TM
Transmembrane

3
LI:204262.2:2001JAN12
333
374
forward 2
TM
Cytosolic

4
LI:331661.1:2001JAN12
1
554
forward 1
TM
Non-cytosolic

4
LI:331661.1:2001JAN12
555
577
forward 1
TM
Transmembrane

4
LI:331661.1:2001JAN12
578
589
forward 1
TM
Cytosolic

5
LI:335074.1:2001JAN12
1
221
forward 1
TM
Cytosolic

6
LI:154608.1:2001JAN12
1
40
forward 2
TM
Cytosolic

6
LI:154608.1:2001JAN12
41
63
forward 2
TM
Transmembrane

6
LI:154608.1:2001JAN12
64
196
forward 2
TM
Non-cytosolic

6
LI:154608.1:2001JAN12
197
219
forward 2
TM
Transmembrane

6
LI:154608.1:2001JAN12
220
252
forward 2
TM
Cytosolic

7
LI:462889.1:2001JAN12
1
155
forward 3
TM
Cytosolic

7
LI:462889.1:2001JAN12
156
178
forward 3
TM
Transmembrane

7
LI:462889.1:2001JAN12
179
239
forward 3
TM
Non-cytosolic

8
LI:236680.2:2001JAN12
1
4
forward 1
TM
Non-cytosolic

8
LI:236680.2:2001JAN12
5
27
forward 1
TM
Transmembrane

8
LI:236680.2:2001JAN12
28
47
forward 1
TM
Cytosolic

8
LI:236680.2:2001JAN12
48
67
forward 1
TM
Transmembrane

8
LI:236680.2:2001JAN12
68
777
forward 1
TM
Non-cytosolic

8
LI:236680.2:2001JAN12
1
48
forward 2
TM
Non-cytosolic

8
LI:236680.2:2001JAN12
49
71
forward 2
TM
Transmembrane

8
LI:236680.2:2001JAN12
72
83
forward 2
TM
Cytosolic

8
LI:236680.2:2001JAN12
84
106
forward 2
TM
Transmembrane

8
LI:236680.2:2001JAN12
107
777
forward 2
TM
Non-cytosolic

8
LI:236680.2:2001JAN12
1
19
forward 3
TM
Cytosolic

8
LI:236680.2:2001JAN12
20
42
forward 3
TM
Transmembrane

8
LI:236680.2:2001JAN12
43
777
forward 3
TM
Non-cytosolic

9
LI:228186.1:2001JAN12
1
14
forward 1
TM
Non-cytosolic

9
LI:228186.1:2001JAN12
15
37
forward 1
TM
Transmembrane

9
LI:228186.1:2001JAN12
38
84
forward 1
TM
Cytosolic

9
LI:228186.1:2001JAN12
85
107
forward 1
TM
Transmembrane

9
LI:228186.1:2001JAN12
108
1670
forward 1
TM
Non-cytosolic

9
LI:228186.1:2001JAN12
1
19
forward 2
TM
Non-cytosolic

9
LI:228186.1:2001JAN12
20
39
forward 2
TM
Transmembrane

9
LI:228186.1:2001JAN12
40
51
forward 2
TM
Cytosolic

9
LI:228186.1:2001JAN12
52
74
forward 2
TM
Transmembrane

9
LI:228186.1:2001JAN12
75
387
forward 2
TM
Non-cytosolic

9
LI:228186.1:2001JAN12
388
410
forward 2
TM
Transmembrane

9
LI:228186.1:2001JAN12
411
447
forward 2
TM
Cytosolic

9
LI:228186.1:2001JAN12
448
467
forward 2
TM
Transmembrane

9
LI:228186.1:2001JAN12
468
476
forward 2
TM
Non-cytosolic

9
LI:228186.1:2001JAN12
477
499
forward 2
TM
Transmembrane

9
LI:228186.1:2001JAN12
500
511
forward 2
TM
Cytosolic

9
LI:228186.1:2001JAN12
512
534
forward 2
TM
Transmembrane

9
LI:228186.1:2001JAN12
535
1231
forward 2
TM
Non-cytosolic

9
LI:228186.1:2001JAN12
1232
1254
forward 2
TM
Transmembrane

9
LI:228186.1:2001JAN12
1255
1392
forward 2
TM
Cytosolic

9
LI:228186.1:2001JAN12
1393
1415
forward 2
TM
Transmembrane

9
LI:228186.1:2001JAN12
1416
1670
forward 2
TM
Non-cytosolic

9
LI:228186.1:2001JAN12
1
21
forward 3
TM
Cytosolic

9
LI:228186.1:2001JAN12
22
41
forward 3
TM
Transmembrane

9
LI:228186.1:2001JAN12
42
55
forward 3
TM
Non-cytosolic

9
LI:228186.1:2001JAN12
56
78
forward 3
TM
Transmembrane

9
LI:228186.1:2001JAN12
79
84
forward 3
TM
Cytosolic

9
LI:228186.1:2001JAN12
85
107
forward 3
TM
Transmembrane

9
LI:228186.1:2001JAN12
108
1181
forward 3
TM
Non-cytosolic

9
LI:228186.1:2001JAN12
1182
1204
forward 3
TM
Transmembrane

9
LI:228186.1:2001JAN12
1205
1260
forward 3
TM
Cytosolic

9
LI:228186.1:2001JAN12
1261
1283
forward 3
TM
Transmembrane

9
LI:228186.1:2001JAN12
1284
1670
forward 3
TM
Non-cytosolic

10
LI:721233.1:2001JAN12
1
175
forward 2
TM
Cytosolic

10
LI:721233.1:2001JAN12
176
198
forward 2
TM
Transmembrane

10
LI:721233.1:2001JAN12
199
217
forward 2
TM
Non-cytosolic

11
LI:291759.2:2001JAN12
1
116
forward 1
TM
Cytosolic

11
LI:291759.2:2001JAN12
117
139
forward 1
TM
Transmembrane

11
LI:291759.2:2001JAN12
140
423
forward 1
TM
Non-cytosolic

11
LI:291759.2:2001JAN12
1
192
forward 2
TM
Cytosolic

11
LI:291759.2:2001JAN12
193
215
forward 2
TM
Transmembrane

11
LI:291759.2:2001JAN12
216
423
forward 2
TM
Non-cytosolic

12
LI:292613.17:2001JAN12
1
14
forward 1
TM
Non-cytosolic

12
LI:292613.17:2001JAN12
15
33
forward 1
TM
Transmembrane

12
LI:292613.17:2001JAN12
34
121
forward 1
TM
Cytosolic

12
LI:292613.17:2001JAN12
1
56
forward 2
TM
Cytosolic

12
LI:292613.17:2001JAN12
57
79
forward 2
TM
Transmembrane

12
LI:292613.17:2001JAN12
80
120
forward 2
TM
Non-cytosolic

12
LI:292613.17:2001JAN12
1
120
forward 3
TM
Cytosolic

13
LI:412959.15:2001JAN12
1
52
forward 1
TM
Non-cytosolic

13
LI:412959.15:2001JAN12
53
75
forward 1
TM
Transmembrane

13
LI:412959.15:2001JAN12
76
95
forward 1
TM
Cytosolic

13
LI:412959.15:2001JAN12
96
118
forward 1
TM
Transmembrane

13
LI:412959.15:2001JAN12
119
137
forward 1
TM
Non-cytosolic

13
LI:412959.15:2001JAN12
138
160
forward 1
TM
Transmembrane

13
LI:412959.15:2001JAN12
161
164
forward 1
TM
Cytosolic

13
LI:412959.15:2001JAN12
165
183
forward 1
TM
Transmembrane

13
LI:412959.15:2001JAN12
184
187
forward 1
TM
Non-cytosolic

13
LI:412959.15:2001JAN12
1
33
forward 2
TM
Non-cytosolic

13
LI:412959.15:2001JAN12
34
56
forward 2
TM
Transmembrane

13
LI:412959.15:2001JAN12
57
95
forward 2
TM
Cytosolic

13
LI:412959.15:2001JAN12
96
118
forward 2
TM
Transmembrane

13
LI:412959.15:2001JAN12
119
127
forward 2
TM
Non-cytosolic

13
LI:412959.15:2001JAN12
128
145
forward 2
TM
Transmembrane

13
LI:412959.15:2001JAN12
146
149
forward 2
TM
Cytosolic

13
LI:412959.15:2001JAN12
150
169
forward 2
TM
Transmembrane

13
LI:412959.15:2001JAN12
170
187
forward 2
TM
Non-cytosolic

13
LI:412959.15:2001JAN12
1
125
forward 3
TM
Cytosolic

13
LI:412959.15:2001JAN12
126
148
forward 3
TM
Transmembrane

13
LI:412959.15:2001JAN12
149
187
forward 3
TM
Non-cytosolic

14
LI:482512.3:2001JAN12
1
767
forward 2
TM
Non-cytosolic

14
LI:482512.3:2001JAN12
768
790
forward 2
TM
Transmembrane

14
LI:482512.3:2001JAN12
791
806
forward 2
TM
Cytosolic

15
LI:413231.6:2001JAN12
1
231
forward 1
TM
Non-cytosolic

15
LI:413231.6:2001JAN12
232
254
forward 1
TM
Transmembrane

15
LI:413231.6:2001JAN12
255
274
forward 1
TM
Cytosolic

15
LI:413231.6:2001JAN12
275
297
forward 1
TM
Transmembrane

15
LI:413231.6:2001JAN12
298
332
forward 1
TM
Non-cytosolic

16
LI:203383.1:2001JAN12
1
12
forward 1
TM
Cytosolic

16
LI:203383.1:2001JAN12
13
32
forward 1
TM
Transmembrane

16
LI:203383.1:2001JAN12
33
414
forward 1
TM
Non-cytosolic

16
LI:203383.1:2001JAN12
1
12
forward 2
TM
Cytosolic

16
LI:203383.1:2001JAN12
13
35
forward 2
TM
Transmembrane

16
LI:203383.1:2001JAN12
36
413
forward 2
TM
Non-cytosolic

16
LI:203383.1:2001JAN12
1
12
forward 3
TM
Cytosolic

16
LI:203383.1:2001JAN12
13
35
forward 3
TM
Transmembrane

16
LI:203383.1:2001JAN12
36
413
forward 3
TM
Non-cytosolic

17
LI:133186.4:2001JAN12
1
25
forward 1
TM
Non-cytosolic

17
LI:133186.4:2001JAN12
26
48
forward 1
TM
Transmembrane

17
LI:133186.4:2001JAN12
49
52
forward 1
TM
Cytosolic

17
LI:133186.4:2001JAN12
53
75
forward 1
TM
Transmembrane

17
LI:133186.4:2001JAN12
76
89
forward 1
TM
Non-cytosolic

17
LI:133186.4:2001JAN12
90
107
forward 1
TM
Transmembrane

17
LI:133186.4:2001JAN12
108
119
forward 1
TM
Cytosolic

17
LI:133186.4:2001JAN12
120
142
forward 1
TM
Transmembrane

17
LI:133186.4:2001JAN12
143
192
forward 1
TM
Non-cytosolic

17
LI:133186.4:2001JAN12
1
20
forward 2
TM
Cytosolic

17
LI:133186.4:2001JAN12
21
43
forward 2
TM
Transmembrane

17
LI:133186.4:2001JAN12
44
192
forward 2
TM
Non-cytosolic

17
LI:133186.4:2001JAN12
1
61
forward 3
TM
Non-cytosolic

17
LI:133186.4:2001JAN12
62
84
forward 3
TM
Transmembrane

17
LI:133186.4:2001JAN12
85
191
forward 3
TM
Cytosolic

18
LI:238576.2:2001JAN12
1
257
forward 1
TM
Non-cytosolic

18
LI:238576.2:2001JAN12
258
280
forward 1
TM
Transmembrane

18
LI:238576.2:2001JAN12
281
449
forward 1
TM
Cytosolic

19
LI:903914.3:2001JAN12
1
607
forward 1
TM
Non-cytosolic

19
LI:903914.3:2001JAN12
608
630
forward 1
TM
Transmembrane

19
LI:903914.3:2001JAN12
631
917
forward 1
TM
Cytosolic

19
LI:903914.3:2001JAN12
918
940
forward 1
TM
Transmembrane

19
LI:903914.3:2001JAN12
941
1420
forward 1
TM
Non-cytosolic

19
LI:903914.3:2001JAN12
1421
1443
forward 1
TM
Transmembrane

19
LI:903914.3:2001JAN12
1444
1596
forward 1
TM
Cytosolic

19
LI:903914.3:2001JAN12
1597
1619
forward 1
TM
Transmembrane

19
LI:903914.3:2001JAN12
1620
1628
forward 1
TM
Non-cytosolic

19
LI:903914.3:2001JAN12
1629
1651
forward 1
TM
Transmembrane

19
LI:903914.3:2001JAN12
1652
1657
forward 1
TM
Cytosolic

19
LI:903914.3:2001JAN12
1658
1680
forward 1
TM
Transmembrane

19
LI:903914.3:2001JAN12
1681
2477
forward 1
TM
Non-cytosolic

19
LI:903914.3:2001JAN12
1
313
forward 2
TM
Non-cytosolic

19
LI:903914.3:2001JAN12
314
336
forward 2
TM
Transmembrane

19
LI:903914.3:2001JAN12
337
342
forward 2
TM
Cytosolic

19
LI:903914.3:2001JAN12
343
362
forward 2
TM
Transmembrane

19
LI:903914.3:2001JAN12
363
366
forward 2
TM
Non-cytosolic

19
LI:903914.3:2001JAN12
367
389
forward 2
TM
Transmembrane

19
LI:903914.3:2001JAN12
390
409
forward 2
TM
Cytosolic

19
LI:903914.3:2001JAN12
410
432
forward 2
TM
Transmembrane

19
LI:903914.3:2001JAN12
433
446
forward 2
TM
Non-cytosolic

19
LI:903914.3:2001JAN12
447
466
forward 2
TM
Transmembrane

19
LI:903914.3:2001JAN12
467
579
forward 2
TM
Cytosolic

19
LI:903914.3:2001JAN12
580
598
forward 2
TM
Transmembrane

19
LI:903914.3:2001JAN12
599
607
forward 2
TM
Non-cytosolic

19
LI:903914.3:2001JAN12
608
630
forward 2
TM
Transmembrane

19
LI:903914.3:2001JAN12
631
678
forward 2
TM
Cytosolic

19
LI:903914.3:2001JAN12
679
701
forward 2
TM
Transmembrane

19
LI:903914.3:2001JAN12
702
845
forward 2
TM
Non-cytosolic

19
LI:903914.3:2001JAN12
846
868
forward 2
TM
Transmembrane

19
LI:903914.3:2001JAN12
869
1071
forward 2
TM
Cytosolic

19
LI:903914.3:2001JAN12
1072
1094
forward 2
TM
Transmembrane

19
LI:903914.3:2001JAN12
1095
2476
forward 2
TM
Non-cytosolic

19
LI:903914.3:2001JAN12
1
1157
forward 3
TM
Non-cytosolic

19
LI:903914.3:2001JAN12
1158
1177
forward 3
TM
Transmembrane

19
LI:903914.3:2001JAN12
1178
1419
forward 3
TM
Cytosolic

19
LI:903914.3:2001JAN12
1420
1442
forward 3
TM
Transmembrane

19
LI:903914.3:2001JAN12
1443
1456
forward 3
TM
Non-cytosolic

19
LI:903914.3:2001JAN12
1457
1479
forward 3
TM
Transmembrane

19
LI:903914.3:2001JAN12
1480
1499
forward 3
TM
Cytosolic

19
LI:903914.3:2001JAN12
1500
1522
forward 3
TM
Transmembrane

19
LI:903914.3:2001JAN12
1523
2476
forward 3
TM
Non-cytosolic

20
LI:150817.1:2001JAN12
1
6
forward 1
TM
Cytosolic

20
LI:150817.1:2001JAN12
7
29
forward 1
TM
Transmembrane

20
LI:150817.1:2001JAN12
30
38
forward 1
TM
Non-cytosolic

20
LI:150817.1:2001JAN12
39
61
forward 1
TM
Transmembrane

20
LI:150817.1:2001JAN12
62
81
forward 1
TM
Cytosolic

20
LI:150817.1:2001JAN12
82
104
forward 1
TM
Transmembrane

20
LI:150817.1:2001JAN12
105
1471
forward 1
TM
Non-cytosolic

20
LI:150817.1:2001JAN12
1
37
forward 3
TM
Cytosolic

20
LI:150817.1:2001JAN12
38
60
forward 3
TM
Transmembrane

20
LI:150817.1:2001JAN12
61
87
forward 3
TM
Non-cytosolic

20
LI:150817.1:2001JAN12
88
110
forward 3
TM
Transmembrane

20
LI:150817.1:2001JAN12
111
336
forward 3
TM
Cytosolic

20
LI:150817.1:2001JAN12
337
359
forward 3
TM
Transmembrane

20
LI:150817.1:2001JAN12
360
798
forward 3
TM
Non-cytosolic

20
LI:150817.1:2001JAN12
799
821
forward 3
TM
Transmembrane

20
LI:150817.1:2001JAN12
822
1024
forward 3
TM
Cytosolic

20
LI:150817.1:2001JAN12
1025
1047
forward 3
TM
Transmembrane

20
LI:150817.1:2001JAN12
1048
1471
forward 3
TM
Non-cytosolic

21
LI:219627.1:2001JAN12
1
19
forward 1
TM
Cytosolic

21
LI:219627.1:2001JAN12
20
42
forward 1
TM
Transmembrane

21
LI:219627.1:2001JAN12
43
117
forward 1
TM
Non-cytosolic

21
LI:219627.1:2001JAN12
118
140
forward 1
TM
Transmembrane

21
LI:219627.1:2001JAN12
141
399
forward 1
TM
Cytosolic

21
LI:219627.1:2001JAN12
400
419
forward 1
TM
Transmembrane

21
LI:219627.1:2001JAN12
420
428
forward 1
TM
Non-cytosolic

21
LI:219627.1:2001JAN12
429
451
forward 1
TM
Transmembrane

21
LI:219627.1:2001JAN12
452
520
forward 1
TM
Cytosolic

21
LI:219627.1:2001JAN12
521
543
forward 1
TM
Transmembrane

21
LI:219627.1:2001JAN12
544
719
forward 1
TM
Non-cytosolic

21
LI:219627.1:2001JAN12
1
523
forward 2
TM
Non-cytosolic

21
LI:219627.1:2001JAN12
524
546
forward 2
TM
Transmembrane

21
LI:219627.1:2001JAN12
547
676
forward 2
TM
Cytosolic

21
LI:219627.1:2001JAN12
677
699
forward 2
TM
Transmembrane

21
LI:219627.1:2001JAN12
700
719
forward 2
TM
Non-cytosolic

21
LI:219627.1:2001JAN12
1
3
forward 3
TM
Non-cytosolic

21
LI:219627.1:2001JAN12
4
20
forward 3
TM
Transmembrane

21
LI:219627.1:2001JAN12
21
26
forward 3
TM
Cytosolic

21
LI:219627.1:2001JAN12
27
49
forward 3
TM
Transmembrane

21
LI:219627.1:2001JAN12
50
116
forward 3
TM
Non-cytosolic

21
LI:219627.1:2001JAN12
117
139
forward 3
TM
Transmembrane

21
LI:219627.1:2001JAN12
140
223
forward 3
TM
Cytosolic

21
LI:219627.1:2001JAN12
224
246
forward 3
TM
Transmembrane

21
LI:219627.1:2001JAN12
247
255
forward 3
TM
Non-cytosolic

21
LI:219627.1:2001JAN12
256
278
forward 3
TM
Transmembrane

21
LI:219627.1:2001JAN12
279
509
forward 3
TM
Cytosolic

21
LI:219627.1:2001JAN12
510
532
forward 3
TM
Transmembrane

21
LI:219627.1:2001JAN12
533
535
forward 3
TM
Non-cytosolic

21
LI:219627.1:2001JAN12
536
558
forward 3
TM
Transmembrane

21
LI:219627.1:2001JAN12
559
665
forward 3
TM
Cytosolic

21
LI:219627.1:2001JAN12
666
688
forward 3
TM
Transmembrane

21
LI:219627.1:2001JAN12
689
692
forward 3
TM
Non-cytosolic

21
LI:219627.1:2001JAN12
693
715
forward 3
TM
Transmembrane

21
LI:219627.1:2001JAN12
716
718
forward 3
TM
Cytosolic

22
LI:197812.4:2001JAN12
1
14
forward 1
TM
Non-cytosolic

22
LI:197812.4:2001JAN12
15
34
forward 1
TM
Transmembrane

22
LI:197812.4:2001JAN12
35
107
forward 1
TM
Cytosolic

22
LI:197812.4:2001JAN12
1
53
forward 2
TM
Non-cytosolic

22
LI:197812.4:2001JAN12
54
76
forward 2
TM
Transmembrane

22
LI:197812.4:2001JAN12
77
106
forward 2
TM
Cytosolic

22
LI:197812.4:2001JAN12
1
52
forward 3
TM
Cytosolic

22
LI:197812.4:2001JAN12
53
75
forward 3
TM
Transmembrane

22
LI:197812.4:2001JAN12
76
106
forward 3
TM
Non-cytosolic

23
LI:101525.1:2001JAN12
1
209
forward 2
TM
Cytosolic

23
LI:101525.1:2001JAN12
210
232
forward 2
TM
Transmembrane

23
LI:101525.1:2001JAN12
233
257
forward 2
TM
Non-cytosolic

23
LI:101525.1:2001JAN12
258
280
forward 2
TM
Transmembrane

23
LI:101525.1:2001JAN12
281
300
forward 2
TM
Cytosolic

23
LI:101525.1:2001JAN12
301
318
forward 2
TM
Transmembrane

23
LI:101525.1:2001JAN12
319
327
forward 2
TM
Non-cytosolic

23
LI:101525.1:2001JAN12
328
350
forward 2
TM
Transmembrane

23
LI:101525.1:2001JAN12
351
361
forward 2
TM
Cytosolic

23
LI:101525.1:2001JAN12
362
379
forward 2
TM
Transmembrane

23
LI:101525.1:2001JAN12
380
770
forward 2
TM
Non-cytosolic

23
LI:101525.1:2001JAN12
1
209
forward 3
TM
Cytosolic

23
LI:101525.1:2001JAN12
210
232
forward 3
TM
Transmembrane

23
LI:101525.1:2001JAN12
233
769
forward 3
TM
Non-cytosolic

24
LI:891123.1:2001JAN12
1
92
forward 1
TM
Cytosolic

24
LI:891123.1:2001JAN12
93
115
forward 1
TM
Transmembrane

24
LI:891123.1:2001JAN12
116
124
forward 1
TM
Non-cytosolic

24
LI:891123.1:2001JAN12
125
147
forward 1
TM
Transmembrane

24
LI:891123.1:2001JAN12
148
326
forward 1
TM
Cytosolic

25
LI:813500.1:2001JAN12
1
388
forward 1
TM
Non-cytosolic

25
LI:813500.1:2001JAN12
389
411
forward 1
TM
Transmembrane

25
LI:813500.1:2001JAN12
412
691
forward 1
TM
Cytosolic

25
LI:813500.1:2001JAN12
1
157
forward 3
TM
Non-cytosolic

25
LI:813500.1:2001JAN12
158
180
forward 3
TM
Transmembrane

25
LI:813500.1:2001JAN12
181
184
forward 3
TM
Cytosolic

25
LI:813500.1:2001JAN12
185
207
forward 3
TM
Transmembrane

25
LI:813500.1:2001JAN12
208
221
forward 3
TM
Non-cytosolic

25
LI:813500.1:2001JAN12
222
244
forward 3
TM
Transmembrane

25
LI:813500.1:2001JAN12
245
537
forward 3
TM
Cytosolic

25
LI:813500.1:2001JAN12
538
560
forward 3
TM
Transmembrane

25
LI:813500.1:2001JAN12
561
691
forward 3
TM
Non-cytosolic

26
LI:1037251.1:2001JAN12
1
59
forward 1
TM
Non-cytosolic

26
LI:1037251.1:2001JAN12
60
82
forward 1
TM
Transmembrane

26
LI:1037251.1:2001JAN12
83
221
forward 1
TM
Cytosolic

26
LI:1037251.1:2001JAN12
222
244
forward 1
TM
Transmembrane

26
LI:1037251.1:2001JAN12
245
263
forward 1
TM
Non-cytosolic

26
LI:1037251.1:2001JAN12
264
286
forward 1
TM
Transmembrane

26
LI:1037251.1:2001JAN12
287
428
forward 1
TM
Cytosolic

26
LI:1037251.1:2001JAN12
429
451
forward 1
TM
Transmembrane

26
LI:1037251.1:2001JAN12
452
614
forward 1
TM
Non-cytosolic

26
LI:1037251.1:2001JAN12
615
637
forward 1
TM
Transmembrane

26
LI:1037251.1:2001JAN12
638
653
forward 1
TM
Cytosolic

26
LI:1037251.1:2001JAN12
1
171
forward 2
TM
Cytosolic

26
LI:1037251.1:2001JAN12
172
191
forward 2
TM
Transmembrane

26
LI:1037251.1:2001JAN12
192
200
forward 2
TM
Non-cytosolic

26
LI:1037251.1:2001JAN12
201
223
forward 2
TM
Transmembrane

26
LI:1037251.1:2001JAN12
224
267
forward 2
TM
Cytosolic

26
LI:1037251.1:2001JAN12
268
290
forward 2
TM
Transmembrane

26
LI:1037251.1:2001JAN12
291
425
forward 2
TM
Non-cytosolic

26
LI:1037251.1:2001JAN12
426
445
forward 2
TM
Transmembrane

26
LI:1037251.1:2001JAN12
446
564
forward 2
TM
Cytosolic

26
LI:1037251.1:2001JAN12
565
584
forward 2
TM
Transmembrane

26
LI:1037251.1:2001JAN12
585
612
forward 2
TM
Non-cytosolic

26
LI:1037251.1:2001JAN12
613
635
forward 2
TM
Transmembrane

26
LI:1037251.1:2001JAN12
636
652
forward 2
TM
Cytosolic

26
LI:1037251.1:2001JAN12
1
98
forward 3
TM
Cytosolic

26
LI:1037251.1:2001JAN12
99
121
forward 3
TM
Transmembrane

26
LI:1037251.1:2001JAN12
122
262
forward 3
TM
Non-cytosolic

26
LI:1037251.1:2001JAN12
263
285
forward 3
TM
Transmembrane

26
LI:1037251.1:2001JAN12
286
428
forward 3
TM
Cytosolic

26
LI:1037251.1:2001JAN12
429
451
forward 3
TM
Transmembrane

26
LI:1037251.1:2001JAN12
452
652
forward 3
TM
Non-cytosolic

27
LI:2032187.1:2001JAN12
1
14
forward 3
TM
Non-cytosolic

27
LI:2032187.1:2001JAN12
15
36
forward 3
TM
Transmembrane

27
LI:2032187.1:2001JAN12
37
37
forward 3
TM
Cytosolic

27
LI:2032187.1:2001JAN12
38
60
forward 3
TM
Transmembrane

27
LI:2032187.1:2001JAN12
61
480
forward 3
TM
Non-cytosolic

28
LI:347572.1:2001JAN12
1
963
forward 2
TM
Non-cytosolic

28
LI:347572.1:2001JAN12
964
986
forward 2
TM
Transmembrane

28
LI:347572.1:2001JAN12
987
1221
forward 2
TM
Cytosolic

28
LI:347572.1:2001JAN12
1
905
forward 3
TM
Non-cytosolic

28
LI:347572.1:2001JAN12
906
925
forward 3
TM
Transmembrane

28
LI:347572.1:2001JAN12
926
1221
forward 3
TM
Cytosolic

29
LI:007788.1:2001JAN12
1
346
forward 1
TM
Non-cytosolic

29
LI:007788.1:2001JAN12
347
366
forward 1
TM
Transmembrane

29
LI:007788.1:2001JAN12
367
698
forward 1
TM
Cytosolic

29
LI:007788.1:2001JAN12
1
344
forward 2
TM
Cytosolic

29
LI:007788.1:2001JAN12
345
367
forward 2
TM
Transmembrane

29
LI:007788.1:2001JAN12
368
697
forward 2
TM
Non-cytosolic

29
LI:007788.1:2001JAN12
1
342
forward 3
TM
Cytosolic

29
LI:007788.1:2001JAN12
343
365
forward 3
TM
Transmembrane

29
LI:007788.1:2001JAN12
366
697
forward 3
TM
Non-cytosolic

30
LI:336872.1:2001JAN12
1
406
forward 2
TM
Non-cytosolic

30
LI:336872.1:2001JAN12
407
429
forward 2
TM
Transmembrane

30
LI:336872.1:2001JAN12
430
580
forward 2
TM
Cytosolic

31
LI:1143291.1:2001JAN12
1
554
forward 1
TM
Non-cytosolic

31
LI:1143291.1:2001JAN12
555
577
forward 1
TM
Transmembrane

31
LI:1143291.1:2001JAN12
578
623
forward 1
TM
Cytosolic

31
LI:1143291.1:2001JAN12
624
643
forward 1
TM
Transmembrane

31
LI:1143291.1:2001JAN12
644
647
forward 1
TM
Non-cytosolic

32
LI:093477.1:2001JAN12
1
194
forward 1
TM
Non-cytosolic

32
LI:093477.1:2001JAN12
195
217
forward 1
TM
Transmembrane

32
LI:093477.1:2001JAN12
218
243
forward 1
TM
Cytosolic

32
LI:093477.1:2001JAN12
244
263
forward 1
TM
Transmembrane

32
LI:093477.1:2001JAN12
264
509
forward 1
TM
Non-cytosolic

33
LI:222105.1:2001JAN12
1
759
forward 1
TM
Non-cytosolic

33
LI:222105.1:2001JAN12
760
782
forward 1
TM
Transmembrane

33
LI:222105.1:2001JAN12
783
825
forward 1
TM
Cytosolic

33
LI:222105.1:2001JAN12
826
840
forward 1
TM
Transmembrane

33
LI:222105.1:2001JAN12
841
859
forward 1
TM
Non-cytosolic

33
LI:222105.1:2001JAN12
860
882
forward 1
TM
Transmembrane

33
LI:222105.1:2001JAN12
883
905
forward 1
TM
Cytosolic

33
LI:222105.1:2001JAN12
906
928
forward 1
TM
Transmembrane

33
LI:222105.1:2001JAN12
929
947
forward 1
TM
Non-cytosolic

33
LI:222105.1:2001JAN12
948
970
forward 1
TM
Transmembrane

33
LI:222105.1:2001JAN12
971
981
forward 1
TM
Cytosolic

33
LI:222105.1:2001JAN12
1
825
forward 2
TM
Non-cytosolic

33
LI:222105.1:2001JAN12
826
840
forward 2
TM
Transmembrane

33
LI:222105.1:2001JAN12
841
860
forward 2
TM
Cytosolic

33
LI:222105.1:2001JAN12
861
883
forward 2
TM
Transmembrane

33
LI:222105.1:2001JAN12
884
904
forward 2
TM
Non-cytosolic

33
LI:222105.1:2001JAN12
905
927
forward 2
TM
Transmembrane

33
LI:222105.1:2001JAN12
928
981
forward 2
TM
Cytosolic

34
LI:816737.2:2001JAN12
1
753
forward 1
TM
Non-cytosolic

34
LI:816737.2:2001JAN12
754
776
forward 1
TM
Transmembrane

34
LI:816737.2:2001JAN12
777
796
forward 1
TM
Cytosolic

34
LI:816737.2:2001JAN12
797
819
forward 1
TM
Transmembrane

34
LI:816737.2:2001JAN12
820
906
forward 1
TM
Non-cytosolic

34
LI:816737.2:2001JAN12
907
929
forward 1
TM
Transmembrane

34
LI:816737.2:2001JAN12
930
941
forward 1
TM
Cytosolic

34
LI:816737.2:2001JAN12
942
964
forward 1
TM
Transmembrane

34
LI:816737.2:2001JAN12
965
1015
forward 1
TM
Non-cytosolic

34
LI:816737.2:2001JAN12
1016
1038
forward 1
TM
Transmembrane

34
LI:816737.2:2001JAN12
1039
1067
forward 1
TM
Cytosolic

34
LI:816737.2:2001JAN12
1068
1090
forward 1
TM
Transmembrane

34
LI:816737.2:2001JAN12
1091
1125
forward 1
TM
Non-cytosolic

34
LI:816737.2:2001JAN12
1126
1148
forward 1
TM
Transmembrane

34
LI:816737.2:2001JAN12
1149
1167
forward 1
TM
Cytosolic

34
LI:816737.2:2001JAN12
1168
1190
forward 1
TM
Transmembrane

34
LI:816737.2:2001JAN12
1191
1204
forward 1
TM
Non-cytosolic

34
LI:816737.2:2001JAN12
1205
1227
forward 1
TM
Transmembrane

34
LI:816737.2:2001JAN12
1228
1341
forward 1
TM
Cytosolic

34
LI:816737.2:2001JAN12
1
901
forward 2
TM
Non-cytosolic

34
LI:816737.2:2001JAN12
902
924
forward 2
TM
Transmembrane

34
LI:816737.2:2001JAN12
925
1026
forward 2
TM
Cytosolic

34
LI:816737.2:2001JAN12
1027
1046
forward 2
TM
Transmembrane

34
LI:816737.2:2001JAN12
1047
1079
forward 2
TM
Non-cytosolic

34
LI:816737.2:2001JAN12
1080
1102
forward 2
TM
Transmembrane

34
LI:816737.2:2001JAN12
1103
1182
forward 2
TM
Cytosolic

34
LI:816737.2:2001JAN12
1183
1205
forward 2
TM
Transmembrane

34
LI:816737.2:2001JAN12
1206
1219
forward 2
TM
Non-cytosolic

34
LI:816737.2:2001JAN12
1220
1242
forward 2
TM
Transmembrane

34
LI:816737.2:2001JAN12
1243
1341
forward 2
TM
Cytosolic

34
LI:816737.2:2001JAN12
1
302
forward 3
TM
Cytosolic

34
LI:816737.2:2001JAN12
303
325
forward 3
TM
Transmembrane

34
LI:816737.2:2001JAN12
326
364
forward 3
TM
Non-cytosolic

34
LI:816737.2:2001JAN12
365
387
forward 3
TM
Transmembrane

34
LI:816737.2:2001JAN12
388
666
forward 3
TM
Cytosolic

34
LI:816737.2:2001JAN12
667
686
forward 3
TM
Transmembrane

34
LI:816737.2:2001JAN12
687
762
forward 3
TM
Non-cytosolic

34
LI:816737.2:2001JAN12
763
785
forward 3
TM
Transmembrane

34
LI:816737.2:2001JAN12
786
899
forward 3
TM
Cytosolic

34
LI:816737.2:2001JAN12
900
922
forward 3
TM
Transmembrane

34
LI:816737.2:2001JAN12
923
941
forward 3
TM
Non-cytosolic

34
LI:816737.2:2001JAN12
942
960
forward 3
TM
Transmembrane

34
LI:816737.2:2001JAN12
961
966
forward 3
TM
Cytosolic

34
LI:816737.2:2001JAN12
967
989
forward 3
TM
Transmembrane

34
LI:816737.2:2001JAN12
990
1024
forward 3
TM
Non-cytosolic

34
LI:816737.2:2001JAN12
1025
1044
forward 3
TM
Transmembrane

34
LI:816737.2:2001JAN12
1045
1188
forward 3
TM
Cytosolic

34
LI:816737.2:2001JAN12
1189
1211
forward 3
TM
Transmembrane

34
LI:816737.2:2001JAN12
1212
1245
forward 3
TM
Non-cytosolic

34
LI:816737.2:2001JAN12
1246
1268
forward 3
TM
Transmembrane

34
LI:816737.2:2001JAN12
1269
1340
forward 3
TM
Cytosolic

35
LI:475524.1:2001JAN12
1
339
forward 3
TM
Non-cytosolic

35
LI:475524.1:2001JAN12
340
362
forward 3
TM
Transmembrane

35
LI:475524.1:2001JAN12
363
557
forward 3
TM
Cytosolic

36
LI:383639.1:2001JAN12
1
172
forward 3
TM
Cytosolic

36
LI:383639.1:2001JAN12
173
192
forward 3
TM
Transmembrane

36
LI:383639.1:2001JAN12
193
206
forward 3
TM
Non-cytosolic

36
LI:383639.1:2001JAN12
207
229
forward 3
TM
Transmembrane

36
LI:383639.1:2001JAN12
230
240
forward 3
TM
Cytosolic

36
LI:383639.1:2001JAN12
241
263
forward 3
TM
Transmembrane

36
LI:383639.1:2001JAN12
264
466
forward 3
TM
Non-cytosolic

36
LI:383639.1:2001JAN12
467
489
forward 3
TM
Transmembrane

36
LI:383639.1:2001JAN12
490
500
forward 3
TM
Cytosolic

36
LI:383639.1:2001JAN12
501
523
forward 3
TM
Transmembrane

36
LI:383639.1:2001JAN12
524
971
forward 3
TM
Non-cytosolic

37
LI:814346.1:2001JAN12
1
314
forward 2
TM
Non-cytosolic

37
LI:814346.1:2001JAN12
315
337
forward 2
TM
Transmembrane

37
LI:814346.1:2001JAN12
338
348
forward 2
TM
Cytosolic

37
LI:814346.1:2001JAN12
349
371
forward 2
TM
Transmembrane

37
LI:814346.1:2001JAN12
372
457
forward 2
TM
Non-cytosolic

37
LI:814346.1:2001JAN12
458
477
forward 2
TM
Transmembrane

37
LI:814346.1:2001JAN12
478
483
forward 2
TM
Cytosolic

37
LI:814346.1:2001JAN12
484
506
forward 2
TM
Transmembrane

37
LI:814346.1:2001JAN12
507
608
forward 2
TM
Non-cytosolic

37
LI:814346.1:2001JAN12
609
631
forward 2
TM
Transmembrane

37
LI:814346.1:2001JAN12
632
767
forward 2
TM
Cytosolic

37
LI:814346.1:2001JAN12
768
790
forward 2
TM
Transmembrane

37
LI:814346.1:2001JAN12
791
818
forward 2
TM
Non-cytosolic

37
LI:814346.1:2001JAN12
819
841
forward 2
TM
Transmembrane

37
LI:814346.1:2001JAN12
842
853
forward 2
TM
Cytosolic

37
LI:814346.1:2001JAN12
854
876
forward 2
TM
Transmembrane

37
LI:814346.1:2001JAN12
877
924
forward 2
TM
Non-cytosolic

37
LI:814346.1:2001JAN12
1
341
forward 3
TM
Non-cytosolic

37
LI:814346.1:2001JAN12
342
364
forward 3
TM
Transmembrane

37
LI:814346.1:2001JAN12
365
370
forward 3
TM
Cytosolic

37
LI:814346.1:2001JAN12
371
393
forward 3
TM
Transmembrane

37
LI:814346.1:2001JAN12
394
483
forward 3
TM
Non-cytosolic

37
LI:814346.1:2001JAN12
484
506
forward 3
TM
Transmembrane

37
LI:814346.1:2001JAN12
507
526
forward 3
TM
Cytosolic

37
LI:814346.1:2001JAN12
527
549
forward 3
TM
Transmembrane

37
LI:814346.1:2001JAN12
550
923
forward 3
TM
Non-cytosolic

38
LI:898195.6:2001JAN12
1
1117
forward 1
TM
Non-cytosolic

38
LI:898195.6:2001JAN12
1118
1140
forward 1
TM
Transmembrane

38
LI:898195.6:2001JAN12
1141
1260
forward 1
TM
Cytosolic

38
LI:898195.6:2001JAN12
1261
1283
forward 1
TM
Transmembrane

38
LI:898195.6:2001JAN12
1284
1318
forward 1
TM
Non-cytosolic

38
LI:898195.6:2001JAN12
1319
1338
forward 1
TM
Transmembrane

38
LI:898195.6:2001JAN12
1339
1384
forward 1
TM
Cytosolic

38
LI:898195.6:2001JAN12
1385
1404
forward 1
TM
Transmembrane

38
LI:898195.6:2001JAN12
1405
1418
forward 1
TM
Non-cytosolic

38
LI:898195.6:2001JAN12
1419
1441
forward 1
TM
Transmembrane

38
LI:898195.6:2001JAN12
1442
1468
forward 1
TM
Cytosolic

38
LI:898195.6:2001JAN12
1
905
forward 2
TM
Non-cytosolic

38
LI:898195.6:2001JAN12
906
928
forward 2
TM
Transmembrane

38
LI:898195.6:2001JAN12
929
969
forward 2
TM
Cytosolic

38
LI:898195.6:2001JAN12
970
992
forward 2
TM
Transmembrane

38
LI:898195.6:2001JAN12
993
1006
forward 2
TM
Non-cytosolic

38
LI:898195.6:2001JAN12
1007
1029
forward 2
TM
Transmembrane

38
LI:898195.6:2001JAN12
1030
1118
forward 2
TM
Cytosolic

38
LI:898195.6:2001JAN12
1119
1141
forward 2
TM
Transmembrane

38
LI:898195.6:2001JAN12
1142
1263
forward 2
TM
Non-cytosolic

38
LI:898195.6:2001JAN12
1264
1286
forward 2
TM
Transmembrane

38
LI:898195.6:2001JAN12
1287
1388
forward 2
TM
Cytosolic

38
LI:898195.6:2001JAN12
1389
1411
forward 2
TM
Transmembrane

38
LI:898195.6:2001JAN12
1412
1420
forward 2
TM
Non-cytosolic

38
LI:898195.6:2001JAN12
1421
1443
forward 2
TM
Transmembrane

38
LI:898195.6:2001JAN12
1444
1468
forward 2
TM
Cytosolic

38
LI:898195.6:2001JAN12
1
974
forward 3
TM
Non-cytosolic

38
LI:898195.6:2001JAN12
975
997
forward 3
TM
Transmembrane

38
LI:898195.6:2001JAN12
998
1120
forward 3
TM
Cytosolic

38
LI:898195.6:2001JAN12
1121
1143
forward 3
TM
Transmembrane

38
LI:898195.6:2001JAN12
1144
1152
forward 3
TM
Non-cytosolic

38
LI:898195.6:2001JAN12
1153
1175
forward 3
TM
Transmembrane

38
LI:898195.6:2001JAN12
1176
1264
forward 3
TM
Cytosolic

38
LI:898195.6:2001JAN12
1265
1284
forward 3
TM
Transmembrane

38
LI:898195.6:2001JAN12
1285
1387
forward 3
TM
Non-cytosolic

38
LI:898195.6:2001JAN12
1388
1410
forward 3
TM
Transmembrane

38
LI:898195.6:2001JAN12
1411
1416
forward 3
TM
Cytosolic

38
LI:898195.6:2001JAN12
1417
1439
forward 3
TM
Transmembrane

38
LI:898195.6:2001JAN12
1440
1467
forward 3
TM
Non-cytosolic

39
LI:210497.2:2001JAN12
1
138
forward 3
TM
Cytosolic

40
LI:110297.4:2001JAN12
1
63
forward 1
TM
Cytosolic

40
LI:110297.4:2001JAN12
64
86
forward 1
TM
Transmembrane

40
LI:110297.4:2001JAN12
87
706
forward 1
TM
Non-cytosolic

40
LI:110297.4:2001JAN12
707
724
forward 1
TM
Transmembrane

40
LI:110297.4:2001JAN12
725
760
forward 1
TM
Cytosolic

40
LI:110297.4:2001JAN12
761
783
forward 1
TM
Transmembrane

40
LI:110297.4:2001JAN12
784
792
forward 1
TM
Non-cytosolic

40
LI:110297.4:2001JAN12
793
815
forward 1
TM
Transmembrane

40
LI:110297.4:2001JAN12
816
825
forward 1
TM
Cytosolic

40
LI:110297.4:2001JAN12
1
129
forward 2
TM
Cytosolic

40
LI:110297.4:2001JAN12
130
147
forward 2
TM
Transmembrane

40
LI:110297.4:2001JAN12
148
156
forward 2
TM
Non-cytosolic

40
LI:110297.4:2001JAN12
157
179
forward 2
TM
Transmembrane

40
LI:110297.4:2001JAN12
180
601
forward 2
TM
Cytosolic

40
LI:110297.4:2001JAN12
602
621
forward 2
TM
Transmembrane

40
LI:110297.4:2001JAN12
622
625
forward 2
TM
Non-cytosolic

40
LI:110297.4:2001JAN12
626
648
forward 2
TM
Transmembrane

40
LI:110297.4:2001JAN12
649
761
forward 2
TM
Cytosolic

40
LI:110297.4:2001JAN12
762
784
forward 2
TM
Transmembrane

40
LI:110297.4:2001JAN12
785
798
forward 2
TM
Non-cytosolic

40
LI:110297.4:2001JAN12
799
821
forward 2
TM
Transmembrane

40
LI:110297.4:2001JAN12
822
825
forward 2
TM
Cytosolic

40
LI:110297.4:2001JAN12
1
11
forward 3
TM
Cytosolic

40
LI:110297.4:2001JAN12
12
29
forward 3
TM
Transmembrane

40
LI:110297.4:2001JAN12
30
62
forward 3
TM
Non-cytosolic

40
LI:110297.4:2001JAN12
63
85
forward 3
TM
Transmembrane

40
LI:110297.4:2001JAN12
86
129
forward 3
TM
Cytosolic

40
LI:110297.4:2001JAN12
130
152
forward 3
TM
Transmembrane

40
LI:110297.4:2001JAN12
153
291
forward 3
TM
Non-cytosolic

40
LI:110297.4:2001JAN12
292
314
forward 3
TM
Transmembrane

40
LI:110297.4:2001JAN12
315
326
forward 3
TM
Cytosolic

40
LI:110297.4:2001JAN12
327
349
forward 3
TM
Transmembrane

40
LI:110297.4:2001JAN12
350
363
forward 3
TM
Non-cytosolic

40
LI:110297.4:2001JAN12
364
386
forward 3
TM
Transmembrane

40
LI:110297.4:2001JAN12
387
607
forward 3
TM
Cytosolic

40
LI:110297.4:2001JAN12
608
630
forward 3
TM
Transmembrane

40
LI:110297.4:2001JAN12
631
732
forward 3
TM
Non-cytosolic

40
LI:110297.4:2001JAN12
733
752
forward 3
TM
Transmembrane

40
LI:110297.4:2001JAN12
753
758
forward 3
TM
Cytosolic

40
LI:110297.4:2001JAN12
759
781
forward 3
TM
Transmembrane

40
LI:110297.4:2001JAN12
782
790
forward 3
TM
Non-cytosolic

40
LI:110297.4:2001JAN12
791
813
forward 3
TM
Transmembrane

40
LI:110297.4:2001JAN12
814
824
forward 3
TM
Cytosolic

41
LI:2051312.1:2001JAN12
1
46
forward 1
TM
Cytosolic

41
LI:2051312.1:2001JAN12
47
69
forward 1
TM
Transmembrane

41
LI:2051312.1:2001JAN12
70
542
forward 1
TM
Non-cytosolic

41
LI:2051312.1:2001JAN12
1
36
forward 3
TM
Cytosolic

41
LI:2051312.1:2001JAN12
37
59
forward 3
TM
Transmembrane

41
LI:2051312.1:2001JAN12
60
541
forward 3
TM
Non-cytosolic

42
LI:350272.2:2001JAN12
1
487
forward 1
TM
Non-cytosolic

42
LI:350272.2:2001JAN12
488
510
forward 1
TM
Transmembrane

42
LI:350272.2:2001JAN12
511
519
forward 1
TM
Cytosolic

43
LI:1085472.4:2001JAN12
1
313
forward 1
TM
Cytosolic

43
LI:1085472.4:2001JAN12
314
336
forward 1
TM
Transmembrane

43
LI:1085472.4:2001JAN12
337
713
forward 1
TM
Non-cytosolic

43
LI:1085472.4:2001JAN12
714
736
forward 1
TM
Transmembrane

43
LI:1085472.4:2001JAN12
737
968
forward 1
TM
Cytosolic

43
LI:1085472.4:2001JAN12
969
991
forward 1
TM
Transmembrane

43
LI:1085472.4:2001JAN12
992
1199
forward 1
TM
Non-cytosolic

43
LI:1085472.4:2001JAN12
1
1123
forward 2
TM
Non-cytosolic

43
LI:1085472.4:2001JAN12
1124
1146
forward 2
TM
Transmembrane

43
LI:1085472.4:2001JAN12
1147
1166
forward 2
TM
Cytosolic

43
LI:1085472.4:2001JAN12
1167
1189
forward 2
TM
Transmembrane

43
LI:1085472.4:2001JAN12
1190
1198
forward 2
TM
Non-cytosolic

44
LI:1190272.1:2001JAN12
1
321
forward 1
TM
Non-cytosolic

44
LI:1190272.1:2001JAN12
322
344
forward 1
TM
Transmembrane

44
LI:1190272.1:2001JAN12
345
363
forward 1
TM
Cytosolic

44
LI:1190272.1:2001JAN12
1
311
forward 3
TM
Non-cytosolic

44
LI:1190272.1:2001JAN12
312
334
forward 3
TM
Transmembrane

44
LI:1190272.1:2001JAN12
335
362
forward 3
TM
Cytosolic

45
LI:1086797.1:2001JAN12
1
12
forward 1
TM
Cytosolic

45
LI:1086797.1:2001JAN12
13
35
forward 1
TM
Transmembrane

45
LI:1086797.1:2001JAN12
36
1202
forward 1
TM
Non-cytosolic

45
LI:1086797.1:2001JAN12
1
12
forward 2
TM
Cytosolic

45
LI:1086797.1:2001JAN12
13
35
forward 2
TM
Transmembrane

45
LI:1086797.1:2001JAN12
36
1202
forward 2
TM
Non-cytosolic

45
LI:1086797.1:2001JAN12
1
19
forward 3
TM
Non-cytosolic

45
LI:1086797.1:2001JAN12
20
42
forward 3
TM
Transmembrane

45
LI:1086797.1:2001JAN12
43
172
forward 3
TM
Cytosolic

45
LI:1086797.1:2001JAN12
173
195
forward 3
TM
Transmembrane

45
LI:1086797.1:2001JAN12
196
1013
forward 3
TM
Non-cytosolic

45
LI:1086797.1:2001JAN12
1014
1036
forward 3
TM
Transmembrane

45
LI:1086797.1:2001JAN12
1037
1202
forward 3
TM
Cytosolic

46
LI:1144466.1:2001JAN12
1
690
forward 1
TM
Non-cytosolic

46
LI:1144466.1:2001JAN12
691
710
forward 1
TM
Transmembrane

46
LI:1144466.1:2001JAN12
711
723
forward 1
TM
Cytosolic

46
LI:1144466.1:2001JAN12
1
690
forward 2
TM
Non-cytosolic

46
LI:1144466.1:2001JAN12
691
710
forward 2
TM
Transmembrane

46
LI:1144466.1:2001JAN12
711
723
forward 2
TM
Cytosolic

47
LI:1147914.1:2001JAN12
1
71
forward 2
TM
Cytosolic

47
LI:1147914.1:2001JAN12
72
94
forward 2
TM
Transmembrane

47
LI:1147914.1:2001JAN12
95
464
forward 2
TM
Non-cytosolic

48
LI:758086.1:2001JAN12
1
50
forward 1
TM
Non-cytosolic

48
LI:758086.1:2001JAN12
51
73
forward 1
TM
Transmembrane

48
LI:758086.1:2001JAN12
74
79
forward 1
TM
Cytosolic

48
LI:758086.1:2001JAN12
80
97
forward 1
TM
Transmembrane

48
LI:758086.1:2001JAN12
98
286
forward 1
TM
Non-cytosolic

48
LI:758086.1:2001JAN12
287
309
forward 1
TM
Transmembrane

48
LI:758086.1:2001JAN12
310
329
forward 1
TM
Cytosolic

48
LI:758086.1:2001JAN12
330
352
forward 1
TM
Transmembrane

48
LI:758086.1:2001JAN12
353
464
forward 1
TM
Non-cytosolic

48
LI:758086.1:2001JAN12
1
382
forward 3
TM
Non-cylosolic

48
LI:758086.1:2001JAN12
383
405
forward 3
TM
Transmembrane

48
LI:758086.1:2001JAN12
406
437
forward 3
TM
Cytosolic

48
LI:758086.1:2001JAN12
438
457
forward 3
TM
Transmembrane

48
LI:758086.1:2001JAN12
458
463
forward 3
TM
Non-cytosolic

49
LI:765245.5:2001JAN12
1
351
forward 1
TM
Non-cytosolic

49
LI:765245.5:2001JAN12
352
374
forward 1
TM
Transmembrane

49
LI:765245.5:2001JAN12
375
766
forward 1
TM
Cytosolic

49
LI:765245.5:2001JAN12
1
352
forward 3
TM
Non-cytosolic

49
LI:765245.5:2001JAN12
353
372
forward 3
TM
Transmembrane

49
LI:765245.5:2001JAN12
373
384
forward 3
TM
Cytosolic

49
LI:765245.5:2001JAN12
385
407
forward 3
TM
Transmembrane

49
LI:765245.5:2001JAN12
408
765
forward 3
TM
Non-cytosolic

50
LI:335608.2:2001JAN12
1
19
forward 2
TM
Non-cytosolic

50
LI:335608.2:2001JAN12
20
42
forward 2
TM
Transmembrane

50
LI:335608.2:2001JAN12
43
251
forward 2
TM
Cytosolic

50
LI:335608.2:2001JAN12
252
269
forward 2
TM
Transmembrane

50
LI:335608.2:2001JAN12
270
335
forward 2
TM
Non-cytosolic

50
LI:335608.2:2001JAN12
336
358
forward 2
TM
Transmembrane

50
LI:335608.2:2001JAN12
359
365
forward 2
TM
Cytosolic

50
LI:335608.2:2001JAN12
1
19
forward 3
TM
Non-cytosolic

50
LI:335608.2:2001JAN12
20
42
forward 3
TM
Transmembrane

50
LI:335608.2:2001JAN12
43
53
forward 3
TM
Cytosolic

50
LI:335608.2:2001JAN12
54
76
forward 3
TM
Transmembrane

50
LI:335608.2:2001JAN12
77
251
forward 3
TM
Non-cytosolic

50
LI:335608.2:2001JAN12
252
269
forward 3
TM
Transmembrane

50
LI:335608.2:2001JAN12
270
291
forward 3
TM
Cytosolic

50
LI:335608.2:2001JAN12
292
311
forward 3
TM
Transmembrane

50
LI:335608.2:2001JAN12
312
323
forward 3
TM
Non-cytosolic

50
LI:335608.2:2001JAN12
324
346
forward 3
TM
Transmembrane

50
LI:335608.2:2001JAN12
347
365
forward 3
TM
Cytosolic

51
LI:405795.1:2001JAN12
1
36
forward 1
TM
Cytosolic

51
LI:405795.1:2001JAN12
37
59
forward 1
TM
Transmembrane

51
LI:405795.1:2001JAN12
60
339
forward 1
TM
Non-cytosolic

51
LI:405795.1:2001JAN12
340
362
forward 1
TM
Transmembrane

51
LI:405795.1:2001JAN12
363
692
forward 1
TM
Cytosolic

51
LI:405795.1:2001JAN12
693
715
forward 1
TM
Transmembrane

51
LI:405795.1:2001JAN12
716
719
forward 1
TM
Non-cytosolic

51
LI:405795.1:2001JAN12
720
742
forward 1
TM
Transmembrane

51
LI:405795.1:2001JAN12
743
746
forward 1
TM
Cytosolic

51
LI:405795.1:2001JAN12
1
139
forward 2
TM
Non-cytosolic

51
LI:405795.1:2001JAN12
140
162
forward 2
TM
Transmembrane

51
LI:405795.1:2001JAN12
163
316
forward 2
TM
Cytosolic

51
LI:405795.1:2001JAN12
317
339
forward 2
TM
Transmembrane

51
LI:405795.1:2001JAN12
340
418
forward 2
TM
Non-cytosolic

51
LI:405795.1:2001JAN12
419
441
forward 2
TM
Transmembrane

51
LI:405795.1:2001JAN12
442
699
forward 2
TM
Cytosolic

51
LI:405795.1:2001JAN12
700
722
forward 2
TM
Transmembrane

51
LI:405795.1:2001JAN12
723
745
forward 2
TM
Non-cytosolic

51
LI:405795.1:2001JAN12
1
54
forward 3
TM
Non-cytosolic

51
LI:405795.1:2001JAN12
55
77
forward 3
TM
Transmembrane

51
LI:405795.1:2001JAN12
78
421
forward 3
TM
Cytosolic

51
LI:405795.1:2001JAN12
422
444
forward 3
TM
Transmembrane

51
LI:405795.1:2001JAN12
445
696
forward 3
TM
Non-cytosolic

51
LI:405795.1:2001JAN12
697
719
forward 3
TM
Transmembrane

51
LI:405795.1:2001JAN12
720
745
forward 3
TM
Cytosolic

52
LI:014872.1:2001JAN12
1
44
forward 1
TM
Cytosolic

52
LI:014872.1:2001JAN12
45
64
forward 1
TM
Transmembrane

52
LI:014872.1:2001JAN12
65
97
forward 1
TM
Non-cytosolic

52
LI:014872.1:2001JAN12
98
120
forward 1
TM
Transmembrane

52
LI:014872.1:2001JAN12
121
453
forward 1
TM
Cytosolic

53
LI:239245.3:2001JAN12
1
19
forward 1
TM
Non-cytosolic

53
LI:239245.3:2001JAN12
20
42
forward 1
TM
Transmembrane

53
LI:239245.3:2001JAN12
43
164
forward 1
TM
Cytosolic

53
LI:239245.3:2001JAN12
165
187
forward 1
TM
Transmembrane

53
LI:239245.3:2001JAN12
188
817
forward 1
TM
Non-cytosolic

53
LI:239245.3:2001JAN12
818
840
forward 1
TM
Transmembrane

53
LI:239245.3:2001JAN12
841
877
forward 1
TM
Cytosolic

53
LI:239245.3:2001JAN12
1
810
forward 2
TM
Non-cytosolic

53
LI:239245.3:2001JAN12
811
833
forward 2
TM
Transmembrane

53
LI:239245.3:2001JAN12
834
877
forward 2
TM
Cytosolic

53
LI:239245.3:2001JAN12
1
810
forward 3
TM
Non-cytosolic

53
LI:239245.3:2001JAN12
811
833
forward 3
TM
Transmembrane

53
LI:239245.3:2001JAN12
834
877
forward 3
TM
Cytosolic

54
LI:142384.5:2001JAN12
1
574
forward 2
TM
Non-cytosolic

54
LI:142384.5:2001JAN12
575
597
forward 2
TM
Transmembrane

54
LI:142384.5:2001JAN12
598
725
forward 2
TM
Cytosolic

54
LI:142384.5:2001JAN12
726
748
forward 2
TM
Transmembrane

54
LI:142384.5:2001JAN12
749
752
forward 2
TM
Non-cytosolic

54
LI:142384.5:2001JAN12
753
775
forward 2
TM
Transmembrane

54
LI:142384.5:2001JAN12
776
995
forward 2
TM
Cytosolic

54
LI:142384.5:2001JAN12
996
1015
forward 2
TM
Transmembrane

54
LI:142384.5:2001JAN12
1016
1018
forward 2
TM
Non-cytosolic

55
LI:2068768.1:2001JAN12
1
140
forward 2
TM
Cytosolic

55
LI:2068768.1:2001JAN12
141
163
forward 2
TM
Transmembrane

55
LI:2068768.1:2001JAN12
164
169
forward 2
TM
Non-cytosolic

56
LI:2118074.1:2001JAN12
1
51
forward 3
TM
Cytosolic

56
LI:2118074.1:2001JAN12
52
74
forward 3
TM
Transmembrane

56
LI:2118074.1:2001JAN12
75
88
forward 3
TM
Non-cytosolic

56
LI:2118074.1:2001JAN12
89
106
forward 3
TM
Transmembrane

56
LI:2118074.1:2001JAN12
107
145
forward 3
TM
Cytosolic

56
LI:2118074.1:2001JAN12
146
168
forward 3
TM
Transmembrane

56
LI:2118074.1:2001JAN12
169
178
forward 3
TM
Non-cytosolic

57
LI:1189068.4:2001JAN12
1
562
forward 3
TM
Non-cytosolic

57
LI:1189068.4:2001JAN12
563
585
forward 3
TM
Transmembrane

57
LI:1189068.4:2001JAN12
586
654
forward 3
TM
Cytosolic

58
LI:2118704.1:2001JAN12
1
33
forward 3
TM
Non-cytosolic

58
LI:2118704.1:2001JAN12
34
56
forward 3
TM
Transmembrane

58
LI:2118704.1:2001JAN12
57
60
forward 3
TM
Cytosolic

58
LI:2118704.1:2001JAN12
61
83
forward 3
TM
Transmembrane

58
LI:2118704.1:2001JAN12
84
339
forward 3
TM
Non-cytosolic

59
LI:031700.2:2001JAN12
1
237
forward 1
TM
Cytosolic

59
LI:031700.2:2001JAN12
238
260
forward 1
TM
Transmembrane

59
LI:031700.2:2001JAN12
261
269
forward 1
TM
Non-cytosolic

59
LI:031700.2:2001JAN12
270
292
forward 1
TM
Transmembrane

59
LI:031700.2:2001JAN12
293
389
forward 1
TM
Cytosolic

59
LI:031700.2:2001JAN12
390
412
forward 1
TM
Transmembrane

59
LI:031700.2:2001JAN12
413
847
forward 1
TM
Non-cytosolic

59
LI:031700.2:2001JAN12
1
99
forward 2
TM
Non-cytosolic

59
LI:031700.2:2001JAN12
100
119
forward 2
TM
Transmembrane

59
LI:031700.2:2001JAN12
120
251
forward 2
TM
Cytosolic

59
LI:031700.2:2001JAN12
252
271
forward 2
TM
Transmembrane

59
LI:031700.2:2001JAN12
272
274
forward 2
TM
Non-cytosolic

59
LI:031700.2:2001JAN12
275
294
forward 2
TM
Transmembrane

59
LI:031700.2:2001JAN12
295
388
forward 2
TM
Cytosolic

59
LI:031700.2:2001JAN12
389
411
forward 2
TM
Transmembrane

59
LI:031700.2:2001JAN12
412
420
forward 2
TM
Non-cytosolic

59
LI:031700.2:2001JAN12
421
443
forward 2
TM
Transmembrane

59
LI:031700.2:2001JAN12
444
488
forward 2
TM
Cytosolic

59
LI:031700.2:2001JAN12
489
508
forward 2
TM
Transmembrane

59
LI:031700.2:2001JAN12
509
847
forward 2
TM
Non-cytosolic

59
LI:031700.2:2001JAN12
1
4
forward 3
TM
Non-cytosolic

59
LI:031700.2:2001JAN12
5
22
forward 3
TM
Transmembrane

59
LI:031700.2:2001JAN12
23
97
forward 3
TM
Cytosolic

59
LI:031700.2:2001JAN12
98
120
forward 3
TM
Transmembrane

59
LI:031700.2:2001JAN12
121
245
forward 3
TM
Non-cytosolic

59
LI:031700.2:2001JAN12
246
268
forward 3
TM
Transmembrane

59
LI:031700.2:2001JAN12
269
274
forward 3
TM
Cytosolic

59
LI:031700.2:2001JAN12
275
294
forward 3
TM
Transmembrane

59
LI:031700.2:2001JAN12
295
846
forward 3
TM
Non-cytosolic

60
LI:2120122.1:2001JAN12
1
25
forward 1
TM
Cytosolic

60
LI:2120122.1:2001JAN12
26
48
forward 1
TM
Transmembrane

60
LI:2120122.1:2001JAN12
49
267
forward 1
TM
Non-cytosolic

60
LI:2120122.1:2001JAN12
268
287
forward 1
TM
Transmembrane

60
LI:2120122.1:2001JAN12
288
299
forward 1
TM
Cytosolic

60
LI:2120122.1:2001JAN12
300
322
forward 1
TM
Transmembrane

60
LI:2120122.1:2001JAN12
323
350
forward 1
TM
Non-cytosolic

60
LI:2120122.1:2001JAN12
351
373
forward 1
TM
Transmembrane

60
LI:2120122.1:2001JAN12
374
443
forward 1
TM
Cytosolic

60
LI:2120122.1:2001JAN12
444
466
forward 1
TM
Transmembrane

60
LI:2120122.1:2001JAN12
467
470
forward 1
TM
Non-cytosolic

60
LI:2120122.1:2001JAN12
471
493
forward 1
TM
Transmembrane

60
LI:2120122.1:2001JAN12
494
505
forward 1
TM
Cytosolic

60
LI:2120122.1:2001JAN12
506
528
forward 1
TM
Transmembrane

60
LI:2120122.1:2001JAN12
529
586
forward 1
TM
Non-cytosolic

60
LI:2120122.1:2001JAN12
1
122
forward 2
TM
Non-cytosolic

60
LI:2120122.1:2001JAN12
123
142
forward 2
TM
Transmembrane

60
LI:2120122.1:2001JAN12
143
148
forward 2
TM
Cytosolic

60
LI:2120122.1:2001JAN12
149
171
forward 2
TM
Transmembrane

60
LI:2120122.1:2001JAN12
172
462
forward 2
TM
Non-cytosolic

60
LI:2120122.1:2001JAN12
463
485
forward 2
TM
Transmembrane

60
LI:2120122.1:2001JAN12
486
586
forward 2
TM
Cytosolic

60
LI:2120122.1:2001JAN12
1
23
forward 3
TM
Non-cytosolic

60
LI:2120122.1:2001JAN12
24
46
forward 3
TM
Transmembrane

60
LI:2120122.1:2001JAN12
47
65
forward 3
TM
Cytosolic

60
LI:2120122.1:2001JAN12
66
85
forward 3
TM
Transmembrane

60
LI:2120122.1:2001JAN12
86
254
forward 3
TM
Non-cytosolic

60
LI:2120122.1:2001JAN12
255
277
forward 3
TM
Transmembrane

60
LI:2120122.1:2001JAN12
278
425
forward 3
TM
Cytosolic

60
LI:2120122.1:2001JAN12
426
448
forward 3
TM
Transmembrane

60
LI:2120122.1:2001JAN12
449
467
forward 3
TM
Non-cytosolic

60
LI:2120122.1:2001JAN12
468
490
forward 3
TM
Transmembrane

60
LI:2120122.1:2001JAN12
491
496
forward 3
TM
Cytosolic

60
LI:2120122.1:2001JAN12
497
515
forward 3
TM
Transmembrane

60
LI:2120122.1:2001JAN12
516
585
forward 3
TM
Non-cytosolic

61
LI:816174.1:2001JAN12
1
277
forward 3
TM
Non-cytosolic

61
LI:816174.1:2001JAN12
278
300
forward 3
TM
Transmembrane

61
LI:816174.1:2001JAN12
301
344
forward 3
TM
Cytosolic

62
LI:1189569.11:2001JAN12
1
12
forward 1
TM
Cytosolic

62
LI:1189569.11:2001JAN12
13
35
forward 1
TM
Transmembrane

62
LI:1189569.11:2001JAN12
36
305
forward 1
TM
Non-cytosolic

62
LI:1189569.11:2001JAN12
1
184
forward 2
TM
Non-cytosolic

62
LI:1189569.11:2001JAN12
185
207
forward 2
TM
Transmembrane

62
LI:1189569.11:2001JAN12
208
304
forward 2
TM
Cytosolic

63
LI:413584.1:2001JAN12
1
4
forward 2
TM
Non-cytosolic

63
LI:413584.1:2001JAN12
5
24
forward 2
TM
Transmembrane

63
LI:413584.1:2001JAN12
25
72
forward 2
TM
Cytosolic

63
LI:413584.1:2001JAN12
73
95
forward 2
TM
Transmembrane

63
LI:413584.1:2001JAN12
96
445
forward 2
TM
Non-cytosolic

64
LI:791042.1:2001JAN12
1
392
forward 2
TM
Non-cytosolic

64
LI:791042.1:2001JAN12
393
415
forward 2
TM
Transmembrane

64
LI:791042.1:2001JAN12
416
434
forward 2
TM
Cytosolic

64
LI:791042.1:2001JAN12
435
457
forward 2
TM
Transmembrane

64
LI:791042.1:2001JAN12
458
487
forward 2
TM
Non-cytosolic

65
LI:1167140.1:2001JAN12
1
444
forward 1
TM
Non-cytosolic

65
LI:1167140.1:2001JAN12
445
467
forward 1
TM
Transmembrane

65
LI:1167140.1:2001JAN12
468
519
forward 1
TM
Cytosolic

65
LI:1167140.1:2001JAN12
1
444
forward 2
TM
Non-cytosolic

65
LI:1167140.1:2001JAN12
445
467
forward 2
TM
Transmembrane

65
LI:1167140.1:2001JAN12
468
519
forward 2
TM
Cytosolic

65
LI:1167140.1:2001JAN12
1
367
forward 3
TM
Non-cytosolic

65
LI:1167140.1:2001JAN12
368
387
forward 3
TM
Transmembrane

65
LI:1167140.1:2001JAN12
388
423
forward 3
TM
Cytosolic

65
LI:1167140.1:2001JAN12
424
446
forward 3
TM
Transmembrane

65
LI:1167140.1:2001JAN12
447
450
forward 3
TM
Non-cytosolic

65
LI:1167140.1:2001JAN12
451
473
forward 3
TM
Transmembrane

65
LI:1167140.1:2001JAN12
474
485
forward 3
TM
Cytosolic

65
LI:1167140.1:2001JAN12
486
508
forward 3
TM
Transmembrane

65
LI:1167140.1:2001JAN12
509
518
forward 3
TM
Non-cytosolic

66
LI:054831.1:2001JAN12
1
3
forward 2
TM
Non-cytosolic

66
LI:054831.1:2001JAN12
4
21
forward 2
TM
Transmembrane

66
LI:054831.1:2001JAN12
22
51
forward 2
TM
Cytosolic

66
LI:054831.1:2001JAN12
52
74
forward 2
TM
Transmembrane

66
LI:054831.1:2001JAN12
75
603
forward 2
TM
Non-cytosolic

67
LI:1175083.1:2001JAN12
1
326
forward 3
TM
Non-cytosolic

67
LI:1175083.1:2001JAN12
327
349
forward 3
TM
Transmembrane

67
LI:1175083.1:2001JAN12
350
354
forward 3
TM
Cytosolic

68
LI:2122897.2:2001JAN12
1
402
forward 2
TM
Non-cytosolic

68
LI:2122897.2:2001JAN12
403
425
forward 2
TM
Transmembrane

68
LI:2122897.2:2001JAN12
426
467
forward 2
TM
Cytosolic

68
LI:2122897.2:2001JAN12
1
391
forward 3
TM
Non-cytosolic

68
LI:2122897.2:2001JAN12
392
414
forward 3
TM
Transmembrane

68
LI:2122897.2:2001JAN12
415
466
forward 3
TM
Cytosolic

69
LI:2053195.3:2001JAN12
1
9
forward 3
TM
Non-cytosolic

69
LI:2053195.3:2001JAN12
10
28
forward 3
TM
Transmembrane

69
LI:2053195.3:2001JAN12
29
101
forward 3
TM
Cytosolic

70
LI:439397.6:2001JAN12
1
407
forward 3
TM
Non-cytosolic

70
LI:439397.6:2001JAN12
408
430
forward 3
TM
Transmembrane

70
LI:439397.6:2001JAN12
431
453
forward 3
TM
Cytosolic

71
LI:816379.6:2001JAN12
1
129
forward 1
TM
Cytosolic

71
LI:816379.6:2001JAN12
130
147
forward 1
TM
Transmembrane

71
LI:816379.6:2001JAN12
148
150
forward 1
TM
Non-cytosolic

71
LI:816379.6:2001JAN12
151
173
forward 1
TM
Transmembrane

71
LI:816379.6:2001JAN12
174
211
forward 1
TM
Cytosolic

71
LI:816379.6:2001JAN12
212
234
forward 1
TM
Transmembrane

71
LI:816379.6:2001JAN12
235
633
forward 1
TM
Non-cytosolic

71
LI:816379.6:2001JAN12
634
653
forward 1
TM
Transmembrane

71
LI:816379.6:2001JAN12
654
659
forward 1
TM
Cytosolic

71
LI:816379.6:2001JAN12
660
682
forward 1
TM
Transmembrane

71
LI:816379.6:2001JAN12
683
734
forward 1
TM
Non-cytosolic

71
LI:816379.6:2001JAN12
1
37
forward 2
TM
Non-cytosolic

71
LI:816379.6:2001JAN12
38
60
forward 2
TM
Transmembrane

71
LI:816379.6:2001JAN12
61
79
forward 2
TM
Cytosolic

71
LI:816379.6:2001JAN12
80
102
forward 2
TM
Transmembrane

71
LI:816379.6:2001JAN12
103
144
forward 2
TM
Non-cytosolic

71
LI:816379.6:2001JAN12
145
167
forward 2
TM
Transmembrane

71
LI:816379.6:2001JAN12
168
212
forward 2
TM
Cytosolic

71
LI:816379.6:2001JAN12
213
232
forward 2
TM
Transmembrane

71
LI:816379.6:2001JAN12
233
289
forward 2
TM
Non-cytosolic

71
LI:816379.6:2001JAN12
290
307
forward 2
TM
Transmembrane

71
LI:816379.6:2001JAN12
308
394
forward 2
TM
Cytosolic

71
LI:816379.6:2001JAN12
395
414
forward 2
TM
Transmembrane

71
LI:816379.6:2001JAN12
415
418
forward 2
TM
Non-cytosolic

71
LI:816379.6:2001JAN12
419
441
forward 2
TM
Transmembrane

71
LI:816379.6:2001JAN12
442
447
forward 2
TM
Cytosolic

71
LI:816379.6:2001JAN12
448
470
forward 2
TM
Transmembrane

71
LI:816379.6:2001JAN12
471
734
forward 2
TM
Non-cytosolic

71
LI:816379.6:2001JAN12
1
39
forward 3
TM
Non-cytosolic

71
LI:816379.6:2001JAN12
40
62
forward 3
TM
Transmembrane

71
LI:816379.6:2001JAN12
63
132
forward 3
TM
Cytosolic

71
LI:816379.6:2001JAN12
133
155
forward 3
TM
Transmembrane

71
LI:816379.6:2001JAN12
156
281
forward 3
TM
Non-cytosolic

71
LI:816379.6:2001JAN12
282
304
forward 3
TM
Transmembrane

71
LI:816379.6:2001JAN12
305
399
forward 3
TM
Cytosolic

71
LI:816379.6:2001JAN12
400
422
forward 3
TM
Transmembrane

71
LI:816379.6:2001JAN12
423
436
forward 3
TM
Non-cytosolic

71
LI:816379.6:2001JAN12
437
459
forward 3
TM
Transmembrane

71
LI:816379.6:2001JAN12
460
629
forward 3
TM
Cytosolic

71
LI:816379.6:2001JAN12
630
652
forward 3
TM
Transmembrane

71
LI:816379.6:2001JAN12
653
734
forward 3
TM
Non-cytosolic

72
LI:2123452.4:2001JAN12
1
36
forward 1
TM
Non-cytosolic

72
LI:2123452.4:2001JAN12
37
59
forward 1
TM
Transmembrane

72
LI:2123452.4:2001JAN12
60
60
forward 1
TM
Cytosolic

72
LI:2123452.4:2001JAN12
61
78
forward 1
TM
Transmembrane

72
LI:2123452.4:2001JAN12
79
87
forward 1
TM
Non-cytosolic

72
LI:2123452.4:2001JAN12
88
110
forward 1
TM
Transmembrane

72
LI:2123452.4:2001JAN12
111
156
forward 1
TM
Cytosolic

72
LI:2123452.4:2001JAN12
1
28
forward 2
TM
Cytosolic

72
LI:2123452.4:2001JAN12
29
51
forward 2
TM
Transmembrane

72
LI:2123452.4:2001JAN12
52
65
forward 2
TM
Non-cytosolic

72
LI:2123452.4:2001JAN12
66
88
forward 2
TM
Transmembrane

72
LI:2123452.4:2001JAN12
89
156
forward 2
TM
Cytosolic

73
LI:474559.8:2001JAN12
1
110
forward 1
TM
Non-cytosolic

73
LI:474559.8:2001JAN12
111
133
forward 1
TM
Transmembrane

73
LI:474559.8:2001JAN12
134
215
forward 1
TM
Cytosolic

73
LI:474559.8:2001JAN12
1
175
forward 2
TM
Cytosolic

73
LI:474559.8:2001JAN12
176
198
forward 2
TM
Transmembrane

73
LI:474559.8:2001JAN12
199
215
forward 2
TM
Non-cytosolic

73
LI:474559.8:2001JAN12
1
215
forward 3
TM
Cytosolic

74
LI:1089871.1:2001JAN12
1
218
forward 2
TM
Cytosolic

74
LI:1089871.1:2001JAN12
219
241
forward 2
TM
Transmembrane

74
LI:1089871.1:2001JAN12
242
282
forward 2
TM
Non-cytosolic

74
LI:1089871.1:2001JAN12
283
305
forward 2
TM
Transmembrane

74
LI:1089871.1:2001JAN12
306
380
forward 2
TM
Cytosolic

74
LI:1089871.1:2001JAN12
381
400
forward 2
TM
Transmembrane

74
LI:1089871.1:2001JAN12
401
437
forward 2
TM
Non-cytosolic

74
LI:1089871.1:2001JAN12
438
460
forward 2
TM
Transmembrane

74
LI:1089871.1:2001JAN12
461
614
forward 2
TM
Cytosolic

74
LI:1089871.1:2001JAN12
615
637
forward 2
TM
Transmembrane

74
LI:1089871.1:2001JAN12
638
760
forward 2
TM
Non-cytosolic

74
LI:1089871.1:2001JAN12
1
221
forward 3
TM
Cytosolic

74
LI:1089871.1:2001JAN12
222
244
forward 3
TM
Transmembrane

74
LI:1089871.1:2001JAN12
245
271
forward 3
TM
Non-cytosolic

74
LI:1089871.1:2001JAN12
272
289
forward 3
TM
Transmembrane

74
LI:1089871.1:2001JAN12
290
437
forward 3
TM
Cytosolic

74
LI:1089871.1:2001JAN12
438
460
forward 3
TM
Transmembrane

74
LI:1089871.1:2001JAN12
461
760
forward 3
TM
Non-cytosolic

75
LI:289608.1:2001JAN12
1
148
forward 2
TM
Cytosolic

75
LI:289608.1:2001JAN12
149
171
forward 2
TM
Transmembrane

75
LI:289608.1:2001JAN12
172
180
forward 2
TM
Non-cytosolic

75
LI:289608.1:2001JAN12
181
203
forward 2
TM
Transmembrane

75
LI:289608.1:2001JAN12
204
220
forward 2
TM
Cytosolic

75
LI:289608.1:2001JAN12
1
184
forward 3
TM
Non-cytosolic

75
LI:289608.1:2001JAN12
185
207
forward 3
TM
Transmembrane

75
LI:289608.1:2001JAN12
208
219
forward 3
TM
Cytosolic

[0324]

4

TABLE 3

SEQ ID NO:
Template ID
Component ID
Start
Stop

1
LI:418914.1:2001JAN12
4029796F6
268
553

1
LI:418914.1:2001JAN12
4029796H1
268
524

1
LI:418914.1:2001JAN12
g4988429
303
758

1
LI:418914.1:2001JAN12
g1101061
352
513

1
LI:418914.1:2001JAN12
g5633945
359
758

1
LI:418914.1:2001JAN12
g3078225
383
758

1
LI:418914.1:2001JAN12
71259473V1
1063
1416

1
LI:418914.1:2001JAN12
5998440H1
1107
1416

1
LI:418914.1:2001JAN12
5051546T6
1218
1423

1
LI:418914.1:2001JAN12
5834482H1
1349
1507

1
LI:418914.1:2001JAN12
5834482T6
1349
1525

1
LI:418914.1:2001JAN12
7586321H2
646
1257

1
LI:418914.1:2001JAN12
5051546F6
819
1234

1
LI:418914.1:2001JAN12
5051546H1
819
1046

1
LI:418914.1:2001JAN12
8066123J1
833
1401

1
LI:418914.1:2001JAN12
4659880H1
32
279

1
LI:418914.1:2001JAN12
g1126083
166
544

1
LI:418914.1:2001JAN12
4029796T6
261
527

1
LI:418914.1:2001JAN12
5726505H1
1
383

1
LI:418914.1:2001JAN12
046079H1
22
158

2
LI:246108.7:2001JAN12
g1696312
457
748

2
LI:246108.7:2001JAN12
g2194270
434
744

2
LI:246108.7:2001JAN12
3852492T6
196
723

2
LI:246108.7:2001JAN12
6888706J1
48
648

2
LI:246108.7:2001JAN12
3852492F6
148
617

2
LI:246108.7:2001JAN12
3852492H1
149
429

2
LI:246108.7:2001JAN12
g2194338
1
339

3
LI:20426Z.2:2001JAN12
g1267547
815
1122

3
LI:204262.2:2001JAN12
g3037719
822
1113

3
LI:204262.2:2001JAN12
g3330198
830
1115

3
LI:204262.2:2001JAN12
g762085
832
1089

3
LI:204262.2:2001JAN12
g5663772
840
1111

3
LI:204262.2:2001JAN12
g2054071
842
1132

3
LI:204262.2:2001JAN12
g2838446
845
1109

3
LI:204262.2:2001JAN12
g921316
850
1119

3
LI:204262.2:2001JAN12
g921478
856
1090

3
LI:204262.2:2001JAN12
g6401369
869
1115

3
LI:204262.2:2001JAN12
3009683H1
875
1022

3
LI:204262.2:2001JAN12
g5863680
882
1115

3
LI:204262.2:2001JAN12
g5904949
5
398

3
LI:204262.2:2001JAN12
6886754J1
8
371

3
LI:204262.2:2001JAN12
2651027H1
14
269

3
LI:204262.2:2001JAN12
2864552H1
13
311

3
LI:204262.2:2001JAN12
3798411H1
18
295

3
LI:204262.2:2001JAN12
3056428H1
24
239

3
LI:204262.2:2001JAN12
g5325960
165
407

3
LI:204262.2:2001JAN12
4405093H1
177
423

3
LI:204262.2:2001JAN12
7710231H1
197
785

3
LI:204262.2:2001JAN12
1316952H1
200
392

3
LI:204262.2:2001JAN12
5697164H1
208
392

3
LI:204262.2:2001JAN12
g1933501
302
392

3
LI:204262.2:2001JAN12
3085446H1
317
591

3
LI:204262.2:2001JAN12
4370458H1
379
483

3
LI:204262.2:2001JAN12
2429647H1
398
626

3
LI:204262.2:2001JAN12
g1301433
397
758

3
LI:204262.2:2001JAN12
1907484H1
399
658

3
LI:204262.2:2001JAN12
4407466H1
399
654

3
LI:204262.2:2001JAN12
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399
662

3
LI:204262.2:2001JAN12
1907484F6
399
721

3
LI:204262.2:2001JAN12
5905191H1
409
558

3
LI:204262.2:2001JAN12
2905068H1
409
609

3
LI:204262.2:2001JAN12
8180656H1
409
840

3
LI:204262.2:2001JAN12
3669938H1
410
707

3
LI:204262.2:2001JAN12
3168274H1
415
695

3
LI:204262.2:2001JAN12
4370372H1
415
647

3
LI:204262.2:2001JAN12
1704319H1
414
623

3
LI:204262.2:2001JAN12
2113619H1
415
640

3
LI:204262.2:2001JAN12
663536H1
415
645

3
LI:204262.2:2001JAN12
3334434H1
409
540

3
LI:204262.2:2001JAN12
1955142H1
415
609

3
LI:204262.2:2001JAN12
2114652H1
419
688

3
LI:204262.2:2001JAN12
7077958H1
1
378

3
LI:204262.2:2001JAN12
2906317F6
1
373

3
LI:204262.2:2001JAN12
2906317H1
1
306

3
LI:204262.2:2001JAN12
2905586H1
3
269

3
LI:204262.2:2001JAN12
g7317508
4
384

3
LI:204262.2:2001JAN12
6450961H1
5
586

3
LI:204262.2:2001JAN12
2733223H1
483
763

3
LI:204262.2:2001JAN12
5490990H1
483
770

3
LI:20426Z.2:2001JAN12
4367028H1
493
738

3
LI:204262.2:2001JAN12
4368445H1
493
772

3
LI:204262.2:2001JAN12
4376291H1
499
755

3
LI:204262.2:2001JAN12
3427865H1
530
791

3
LI:204262.2:2001JAN12
6206254H1
530
1098

3
LI:204262.2:2001JAN12
g2054234
543
866

3
LI:204262.2:2001JAN12
5789606H1
546
837

3
LI:204262.2:2001JAN12
5795364H1
546
828

3
LI:204262.2:2001JAN12
g4533121
547
1019

3
LI:204262.2:2001JAN12
g847490
562
832

3
LI:204262.2:2001JAN12
g921174
563
873

3
LI:204262.2:2001JAN12
g921384
563
869

3
LI:204262.2:2001JAN12
6517347H1
577
1072

3
LI:204262.2:2001JAN12
190748416
591
981

3
LI:204262.2:2001JAN12
6713444H1
595
1006

3
LI:204262.2:2001JAN12
1569057H1
595
804

3
LI:204262.2:2001JAN12
6715344F8
609
1017

3
LI:204262.2:2001JAN12
g7278310
610
1017

3
LI:204262.2:2001JAN12
2905921H1
614
893

3
LI:204262.2:2001JAN12
g5370364
617
1027

3
LI:204262.2:2001JAN12
6715344F6
616
1006

3
LI:204262.2:2001JAN12
g5740750
617
1022

3
LI:204262.2:2001JAN12
g5510928
618
1017

3
LI:204262.2:2001JAN12
g3744370
626
1022

3
LI:204262.2:2001JAN12
1400614H1
627
860

3
LI:204262.2:2001JAN12
1396990H1
627
866

3
LI:204262.2:2001JAN12
1397508H1
627
870

3
LI:204262.2:2001JAN12
7710231J1
637
1123

3
LI:204262.2:2001JAN12
g4291140
644
1114

3
LI:204262.2:2001JAN12
g5425821
647
1113

3
LI:204262.2:2001JAN12
g5235945
661
1117

3
LI:204262.2:2001JAN12
g4533235
663
1118

3
LI:204262.2:2001JAN12
1333591H1
663
904

3
LI:204262.2:2001JAN12
g4524193
665
1116

3
LI:204262.2:2001JAN12
g8361553
665
1114

3
LI:204262.2:2001JAN12
g6835880
666
1117

3
LI:204262.2:2001JAN12
g4524592
667
1022

3
LI:204262.2:2001JAN12
g5675646
673
1129

3
LI:204262.2:2001JAN12
g5396644
679
1114

3
LI:204262.2:2001JAN12
2905087H1
419
689

3
LI:204262.2:2001JAN12
901294H1
419
717

3
LI:204262.2:2001JAN12
901294R1
419
909

3
LI:204262.2:2001JAN12
3986655H1
421
690

3
LI:204262.2:2001JAN12
g1955172
424
751

3
LI:204262.2:2001JAN12
2908149H1
421
713

3
LI:204262.2:2001JAN12
2904727H1
432
731

3
LI:204262.2:2001JAN12
3762093T6
436
1046

3
LI:204262.2:2001JAN12
3590473H1
452
751

3
LI:204262.2:2001JAN12
g1301395
469
692

3
LI:204262.2:2001JAN12
5101734H1
479
720

3
LI:204262.2:2001JAN12
g5744485
881
1114

3
LI:204262.2:2001JAN12
3513391H1
884
1104

3
LI:204262.2:2001JAN12
625181H1
892
1114

3
LI:204262.2:2001JAN12
g1264641
910
1115

3
LI:204262.2:2001JAN12
g6946728
917
1022

3
LI:204262.2:2001JAN12
5595731H1
1020
1112

3
LI:204262.2:2001JAN12
g2753547
742
932

3
LI:204262.2:2001JAN12
g2902957
742
888

3
LI:204262.2:2001JAN12
g1489513
745
1114

3
LI:204262.2:2001JAN12
g2834856
745
1114

3
LI:204262.2:2001JAN12
g3754537
754
1119

3
LI:204262.2:2001JAN12
g6041209
759
1114

3
LI:204262.2:2001JAN12
g2265306
759
1115

3
LI:204262.2:2001JAN12
g3037803
759
1110

3
LI:204262.2:2001JAN12
g7454306
764
1114

3
LI:204262.2:2001JAN12
g6086744
770
1115

3
LI:204262.2:2001JAN12
g3840509
770
1116

3
LI:204262.2:2001JAN12
2936147H1
771
985

3
LI:204262.2:2001JAN12
g4451711
777
1114

3
LI:204262.2:2001JAN12
1955142T6
780
1074

3
LI:204262.2:2001JAN12
g5913403
780
1109

3
LI:204262.2:2001JAN12
g3307161
783
1123

3
LI:204262.2:2001JAN12
g4269266
783
1110

3
LI:204262.2:2001JAN12
g4112857
784
1115

3
LI:204262.2:2001JAN12
g991164
804
1012

3
LI:204262.2:2001JAN12
g2559590
810
876

3
LI:204262.2:2001JAN12
g750913
810
1105

3
LI:204262.2:2001JAN12
g5765810
812
1115

3
LI:204262.2:2001JAN12
g1955173
681
1109

3
LI:204262.2:2001JAN12
g4313037
683
1123

3
LI:204262.2:2001JAN12
2557311H1
685
931

3
LI:204262.2:2001JAN12
2906317T6
685
1071

3
LI:204262.2:2001JAN12
1890505T6
689
985

3
LI:204262.2:2001JAN12
g5741913
689
1114

3
LI:204262.2:2001JAN12
g5448063
690
1117

3
LI:204262.2:2001JAN12
g3094351
690
1114

3
LI:20426Z.2:2001JAN12
g1435306
695
1083

3
LI:204262.2:2001JAN12
1890505H1
696
967

3
LI;204262.2:2001JAN12
g5394697
696
1114

3
LI:204262.2:2001JAN12
1890505F6
696
1010

3
LI:204262.2:2001JAN12
g7038913
697
1116

3
LI:204262.2:2001JAN12
g3077265
697
1118

3
LI:204262.2:2001JAN12
g847491
703
1088

3
LI:204262.2:2001JAN12
g4148492
697
1114

3
LI:204262.2:2001JAN12
g6568355
697
1023

3
LI:204262.2:2001JAN12
g5746321
702
1117

3
LI:204262.2:2001JAN12
g4217673
705
1114

3
LI:204262.2:2001JAN12
g1489512
707
970

3
LI:204262.2:2001JAN12
g1435257
709
1114

3
LI:204262.2:2001JAN12
g5673804
712
1114

3
LI:204262.2:2001JAN12
92731988
713
1114

3
LI:204262.2:2001JAN12
g3756286
714
1114

3
LI:204262.2:2001JAN12
97458416
716
1121

3
LI:204262.2:2001JAN12
g5632323
716
1116

3
LI:204262.2:2001JAN12
7616816H1
719
1109

3
LI:204262.2:2001JAN12
g2554351
741
1029

4
LI:331661.1:2001JAN12
g2877840
1353
1765

4
LI:331661.1:2001JAN12
1616667T6
1384
1731

4
LI:331661.1:2001JAN12
2245381H1
1387
1631

4
LI:331661.1:2001JAN12
7950056H1
1143
1615

4
LI:331661.1:2001JAN12
7449639T2
1150
1693

4
LI:331661.1:2001JAN12
7323804H1
1246
1770

4
LI:331661.1:2001JAN12
1428450T6
1235
1730

4
LI:331661.1:2001JAN12
92713628
1266
1769

4
LI:331661.1:2001JAN12
5759911H1
1310
1523

4
LI:331661.1:2001JAN12
g3962036
1312
1776

4
LI:331661.1:2001JAN12
g2739724
1322
1768

4
LI:331661.1:2001JAN12
1939356R6
1331
1769

4
LI:331661.1:2001JAN12
1939356H1
1331
1571

4
LI:331661.1:2001JAN12
1939356T6
1332
1729

4
LI:331661.1:2001JAN12
g766482
868
1196

4
LI:331661.1:2001JAN12
261732H1
837
1132

4
LI:331661.1:2001JAN12
6120824H1
867
972

4
LI:331661.1:2001JAN12
6197894H1
748
1245

4
LI:331661.1:2001JAN12
6859071H1
798
1183

4
LI:331661.1:2001JAN12
7581096H1
569
1136

4
LI:331661.1:2001JAN12
5924705H1
589
876

4
LI:331661.1:2001JAN12
4716510H1
591
832

4
LI:331661.1:2001JAN12
6856463H1
601
1076

4
LI:331661.1:2001JAN12
1428450H1
624
862

4
LI:331661.1:2001JAN12
1428450F6
633
1095

4
LI:331661.1:2001JAN12
1229221H1
699
923

4
LI:331661.1:2001JAN12
7588474H1
727
1346

4
LI:331661.1:2001JAN12
7236708H1
728
1287

4
LI:331661.1:2001JAN12
6746047H1
1
522

4
LI:331661.1:2001JAN12
7583035H1
33
489

4
LI:331661.1:2001JAN12
1597748H1
78
196

4
LI:331661.1:2001JAN12
1594986H1
78
289

4
LI:331661.1:2001JAN12
1597748F6
78
558

4
LI:331661.1:2001JAN12
8000502H1
99
616

4
LI:331661.1:2001JAN12
7280607H1
107
182

4
LI:331661.1:2001JAN12
6448061H1
450
861

4
LI:331661.1:2001JAN12
4936496H1
499
776

4
LI:331661.1:2001JAN12
5843854H1
502
758

4
LI:331661.1:2001JAN12
3678519H1
1
152

4
LI:331661.1:2001JAN12
1415113H1
908
1157

4
LI:331661.1:2001JAN12
1413270H1
908
1153

4
LI:331661.1:2001JAN12
6338233H1
872
1400

4
LI:331661.1:2001JAN12
g1195372
880
1001

4
LI:331661.1:2001JAN12
5897575H1
889
1175

4
LI:331661.1:2001JAN12
5614128H1
889
1140

4
LI:331661.1:2001JAN12
5900984H1
889
1150

4
LI:331661.1:2001JAN12
6860421H1
924
1359

4
LI:331661.1:2001JAN12
1616667F6
802
1317

4
LI:331661.1:2001JAN12
5681028H1
822
1075

4
LI:331661.1:2001JAN12
1616624H1
802
1000

4
LI:331661.1:2001JAN12
1616667H1
804
939

4
LI:331661.1:2001JAN12
g2017728
1132
1405

4
LI:331661.1:2001JAN12
2283942T6
1120
1728

4
LI:331661.1:2001JAN12
7950056J1
1131
1701

4
LI:331661.1:2001JAN12
6560062H1
948
1468

4
LI:331661.1:2001JAN12
6560643H1
948
1471

4
LI:331661.1:2001JAN12
3825378H1
993
1288

4
LI:331661.1:2001JAN12
6199688H1
1078
1646

4
LI:331661.1:2001JAN12
2283942R6
1079
1516

4
LI:331661.1:2001JAN12
2283942H1
1079
1294

4
LI:331661.1:2001JAN12
7449843T2
1084
1698

4
LI:331661.1:2001JAN12
6715064H1
1419
1769

4
LI:331661.1:2001JAN12
2040660H1
1420
1691

4
LI:331661.1:2001JAN12
g1192246
1469
1768

4
LI:331661.1:2001JAN12
g823120
1529
1781

4
LI:331661.1:2001JAN12
g561300
1585
1769

4
LI:331661.1:2001JAN12
265807H1
1592
1721

4
LI:331661.1:2001JAN12
g3179666
1616
1772

5
LI:335074.1:2001JAN12
6836554H1
1
188

5
LI:335074.1:2001JAN12
2692045H1
30
172

5
LI:335074.1:2001JAN12
2692045F6
30
520

5
LI:335074.1:2001JAN12
9718636
97
172

5
LI:335074.1:2001JAN12
269204516
448
659

5
LI:335074.1:2001JAN12
g4509645
452
606

5
LI:335074.1:2001JAN12
2950136H1
471
528

5
LI:335074.1:2001JAN12
g718536
489
814

5
LI:335074.1:2001JAN12
2734584H1
521
659

5
LI:335074.1:2001JAN12
2734584F6
521
892

5
LI:335074.1:2001JAN12
503404H1
561
663

5
LI:335074.1:2001JAN12
2756506H1
594
659

6
LI:154608.1:2001JAN12
2279720H1
1
256

6
LI:154608.1:2001JAN12
2279720R6
1
463

6
LI:154608.1:2001JAN12
532191H1
1
240

6
LI:154608.1:2001JAN12
g4850584
53
341

6
LI:154608.1:2001JAN12
g1444656
83
374

6
LI:154608.1:2001JAN12
1832633H1
228
384

6
LI:154608.1:2001JAN12
1832633R6
228
754

6
LI:154608.1:2001JAN12
g1224646
299
730

6
LI:154608.1:2001JAN12
677523H1
535
758

7
LI:462889.1:2001JAN12
6012788F6
1
140

7
LI:462889.1:2001JAN12
6012788F8
1
140

7
LI:462889.1:2001JAN12
6012788H1
1
140

7
LI:462889.1:2001JAN12
601278818
1
67

7
LI:462889.1:2001JAN12
6915723H1
20
570

7
LI:462889.1:2001JAN12
7111920H2
101
719

7
LI:462889.1:2001JAN12
7262741H1
241
767

8
LI:236680.2:2001JAN12
3075331H1
2023
2312

8
LI:236680.2:2001JAN12
5532056H1
2026
2253

8
LI:236680.2:2001JAN12
g2913620
2029
2322

8
LI:236680.2:2001JAN12
481091R1
2037
2316

8
LI:236680.2:2001JAN12
481091H1
2037
2268

8
LI:236680.2:2001JAN12
481091F1
2037
2316

8
LI:236680.2:2001JAN12
642676H1
2042
2289

8
LI:236680.2:2001JAN12
645714H1
2042
2169

8
LI:236680.2:2001JAN12
4370936H1
2047
2322

8
LI:236680.2:2001JAN12
g3178618
2052
2327

8
LI:236680.2:2001JAN12
g1951323
2052
2322

8
LI:236680.2:2001JAN12
4369438H1
2060
2330

8
LI:236680.2:2001JAN12
g2752073
2066
2323

8
LI:236680.2:2001JAN12
g2557232
2074
2321

8
LI:236680.2:2001JAN12
2108868H1
2088
2322

8
LI:236680.2:2001JAN12
g3280026
2001
2327

8
LI:236680.2:2001JAN12
g1885612
2004
2322

8
LI:236680.2:2001JAN12
6891191J1
1218
1684

8
LI:236680.2:2001JAN12
616670H1
1222
1382

8
LI:236680.2:2001JAN12
2599521H1
1225
1536

8
LI:236680.2:2001JAN12
1564553H1
1227
1441

8
LI:236680.2:2001JAN12
1718424H1
1247
1452

8
LI:236680.2:2001JAN12
5734658H1
625
832

8
LI:236680.2:2001JAN12
3141286H1
626
920

8
LI:236680.2:2001JAN12
3118707H1
646
930

8
LI:236680.2:2001JAN12
428922H1
646
717

8
LI:236680.2:2001JAN12
7693331J2
658
1282

8
LI:236680.2:2001JAN12
202067H1
671
1013

8
LI:236680.2:2001JAN12
203102H1
669
1039

8
LI:236680.2:2001JAN12
202742H1
671
1096

8
LI:236680.2:2001JAN12
4656004H1
682
914

8
LI:236680.2:2001JAN12
354907H1
682
877

8
LI:236680.2:2001JAN12
4357096H1
689
802

8
LI:236680.2:2001JAN12
7065493H1
700
1264

8
LI:236680.2:2001JAN12
6443867H1
711
1272

8
LI:236680.2:2001JAN12
7748008H1
733
1315

8
LI:236680.2:2001JAN12
4696835H2
733
998

8
LI:236680.2:2001JAN12
2669248H1
734
974

8
LI:236680.2:2001JAN12
7666743H1
737
1307

8
LI:236680.2:2001JAN12
5138583H1
759
1043

8
LI:236680.2:2001JAN12
6344271H1
773
1064

8
LI:236680.2:2001JAN12
4780947H1
782
1025

8
LI:236680.2:2001JAN12
4442960H1
785
932

8
LI:236680.2:2001JAN12
2019004F6
792
1251

8
LI:236680.2:2001JAN12
2019004H1
792
1018

8
LI:236680.2:2001JAN12
7410429H1
808
1291

8
LI:236680.2:2001JAN12
5653870H1
809
1315

8
LI:236680.2:2001JAN12
4973318H1
823
1113

8
LI:236680.2:2001JAN12
3372215H1
828
1107

8
LI:236680.2:2001JAN12
g2824800
836
1152

8
LI:236680.2:2001JAN12
1834495H1
836
1073

8
LI:236680.2:2001JAN12
4891822H1
843
1099

8
LI:236680.2:2001JAN12
3737008H1
875
1053

8
LI:236680.2:2001JAN12
2222730H1
874
1133

8
LI:236680.2:2001JAN12
3056404H1
872
1187

8
LI:236680.2:2001JAN12
1528744H1
877
1089

8
LI:236680.2:2001JAN12
5832993H1
882
1120

8
LI:236680.2:2001JAN12
g1615059
887
1324

8
LI:236680.2:2001JAN12
5568088H1
893
1138

8
LI:236680.2:2001JAN12
4722031H1
894
1151

8
LI:236680.2:2001JAN12
g5657452
895
1316

8
LI:236680.2:2001JAN12
g4984832
899
1316

8
LI:236680.2:2001JAN12
2322090H1
938
1198

8
LI:236680.2:2001JAN12
1743450R6
940
1477

8
LI:236680.2:2001JAN12
1743450H1
940
1209

8
LI:236680.2:2001JAN12
6881552J1
946
1565

8
LI:236680.2:2001JAN12
1492715H1
947
1175

8
LI:236680.2:2001JAN12
g1439952
949
1265

8
LI:236680.2:2001JAN12
g1745436
987
1320

8
LI:236680.2:2001JAN12
5283518H1
989
1101

8
LI:236680.2:2001JAN12
g4983084
999
1402

8
LI;236680.2:2001JAN12
5196591H1
1006
1219

8
LI:236680.2:2001JAN12
g1980081
1014
1300

8
LI:236680.2:2001JAN12
4585166H1
1029
1287

8
LI:236680.2:2001JAN12
3765524H1
1030
1329

8
LI:236680.2:2001JAN12
1322839H1
1030
1310

8
LI:236680.2:2001JAN12
5153956H1
1032
1278

8
LI:236680.2:2001JAN12
5657480H1
1033
1305

8
LI:236680.2:2001JAN12
g3933002
1040
1316

8
LI:236680.2:2001JAN12
3839495H1
1049
1321

8
LI:236680.2:2001JAN12
1807156H1
1052
1330

8
LI:236680.2:2001JAN12
2958652H1
1053
1317

8
LI:236680.2:2001JAN12
550594H1
1061
1215

8
LI:236680.2:2001JAN12
6130516H1
1065
1223

8
LI:236680.2:2001JAN12
g2437088
1066
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8
LI:236680.2:2001JAN12
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1088
1317

8
LI:236680.2:2001JAN12
4531176H1
1095
1317

8
LI:236680.2:2001JAN12
5350661H1
1111
1317

8
LI:236680.2:2001JAN12
6756226J1
1136
1906

8
LI:236680.2:2001JAN12
4069427H1
1141
1419

8
LI:236680.2:2001JAN12
4441238H1
1145
1230

8
LI:236680.2:2001JAN12
2538184H1
1146
1317

8
LI:236680.2:2001JAN12
4440839H1
1146
1317

8
LI:236680.2:2001JAN12
2323415H1
1149
1310

8
LI:236680.2:2001JAN12
2323415R6
1149
1300

8
LI:236680.2:2001JAN12
4091523H1
1160
1451

8
LI:236680.2:2001JAN12
8180480H1
1168
1804

8
LI:236680.2:2001JAN12
g1275598
1173
1632

8
LI:236680.2:2001JAN12
4300822H1
1174
1453

8
LI:236680.2:2001JAN12
6072812H1
1178
1505

8
LI:236680.2:2001JAN12
4769465H1
1190
1454

8
LI:236680.2:2001JAN12
1785637H1
1190
1443

8
LI:236680.2:2001JAN12
4247606H1
1195
1451

8
LI:236680.2:2001JAN12
7355562H1
1205
1818

8
LI:236680.2:2001JAN12
6588333H1
1
514

8
LI:236680.2:2001JAN12
6928483H1
121
456

8
LI:236680.2:2001JAN12
g6701284
220
854

8
LI:236680.2:2001JAN12
4251648H1
243
519

8
LI:236680.2:2001JAN12
1310590T6
255
816

8
LI:236680.2:2001JAN12
7107227H1
292
544

8
LI:236680.2:2001JAN12
7933938H1
314
951

8
LI:236680.2:2001JAN12
3728470H1
413
724

8
LI:236680.2:2001JAN12
g1615058
408
496

8
LI:236680.2:2001JAN12
6191223H1
413
716

8
LI:236680.2:2001JAN12
6936611H1
419
958

8
LI:236680.2:2001JAN12
5000044H2
440
702

8
LI:236680.2:2001JAN12
341967R6
445
887

8
LI:236680.2:2001JAN12
341967H1
445
552

8
LI:236680.2:2001JAN12
g4762563
444
852

8
LI:236680.2:2001JAN12
6336333H1
453
1006

8
LI:236680.2:2001JAN12
3780470H1
455
782

8
LI:236680.2:2001JAN12
3315977H1
464
744

8
LI:236680.2:2001JAN12
4320212H1
485
767

8
LI:236680.2:2001JAN12
2790779H1
496
782

8
LI:236680.2:2001JAN12
5497625H1
493
706

8
LI:236680.2:2001JAN12
g3918889
505
798

8
LI:236680.2:2001JAN12
5499074H1
497
687

8
LI:236680.2:2001JAN12
3405846H1
499
766

8
LI:236680.2:2001JAN12
2260358H1
527
791

8
LI:236680.2:2001JAN12
351557H1
527
763

8
LI:236680.2:2001JAN12
5906465H1
573
833

8
LI:236680.2:2001JAN12
g1885791
602
851

8
LI:236680.2:2001JAN12
1992305F6
621
1092

8
LI:236680.2:2001JAN12
880170H1
1809
2018

8
LI:236680.2:2001JAN12
20LI4995H1
1808
2063

8
LI:236680.2:2001JAN12
880170R1
1812
2321

8
LI:236680.2:2001JAN12
g2740731
1815
2322

8
LI:236680.2:2001JAN12
1722629H1
1817
2031

8
LI:236680.2:2001JAN12
1414184H1
1820
2081

8
LI:236680.2:2001JAN12
g5425815
1826
2320

8
LI:236680.2:2001JAN12
3470172H1
1837
2117

8
LI:236680.2:2001JAN12
5067002H1
1839
2062

8
LI:236680.2:2001JAN12
g4764199
1849
2325

8
LI:236680.2:2001JAN12
g5675041
1854
2325

8
LI:236680.2:2001JAN12
g1289941
1854
2333

8
LI:236680.2:2001JAN12
g3594344
1855
2327

8
LI:236680.2:2001JAN12
g1886363
1854
2284

8
LI:236680.2:2001JAN12
g1071482
1859
2169

8
LI:236680.2:2001JAN12
2614306T6
1868
2285

8
LI:236680.2:2001JAN12
6123995H1
1874
2220

8
LI:236680.2:2001JAN12
6124095H1
1874
2319

8
LI:236680.2:2001JAN12
g4308115
1878
2322

8
LI:236680.2:2001JAN12
4120305H1
1884
2157

8
LI:236680.2:2001JAN12
2285547H1
1889
2158

8
LI:236680.2:2001JAN12
92903185
1891
2322

8
LI:236680.2:2001JAN12
2717291H1
1899
2156

8
LI:236680.2:2001JAN12
1511984T6
1902
2283

8
LI:236680.2:2001JAN12
g2902705
1903
2319

8
LI:236680.2:2001JAN12
2121490H1
1903
2190

8
LI:236680.2:2001JAN12
6891191H1
1906
2273

8
LI:236680.2:2001JAN12
1531659H1
1907
2125

8
LI:236680.2:2001JAN12
g2901559
1916
2317

8
LI:236680.2:2001JAN12
g1927650
1922
2327

8
LI:236680.2:2001JAN12
g1779557
1920
2322

8
LI:236680.2:2001JAN12
764247H1
1923
2225

8
LI:236680.2:2001JAN12
4909776H1
1922
2211

8
LI:236680.2:2001JAN12
g3246364
1924
2328

8
LI:236680.2:2001JAN12
g6034682
1924
2322

8
LI:236680.2:2001JAN12
g3400920
1928
2322

8
LI:236680.2:2001JAN12
g3921126
1931
2323

8
LI:236680.2:2001JAN12
g2184277
1931
2322

8
LI:236680.2:2001JAN12
g2789087
1931
2322

8
LI:236680.2:2001JAN12
5266178H1
1942
2100

8
LI:236680.2:2001JAN12
5268752H1
1943
2238

8
LI:236680.2:2001JAN12
g6034690
1950
2322

8
LI:236680.2:2001JAN12
g1071376
1960
2318

8
LI:236680.2:2001JAN12
g1190233
1962
2318

8
LI:236680.2:2001JAN12
g3134236
1962
2317

8
LI:236680.2:2001JAN12
g1921221
1962
2313

8
LI:236680.2:2001JAN12
4024449H1
1964
2154

8
LI:236680.2:2001JAN12
6449287H1
1970
2317

8
LI:236680.2:2001JAN12
4029205H1
1975
2241

8
LI:236680.2:2001JAN12
6446287H1
1974
2317

8
LI:236680.2:2001JAN12
1384614H1
1985
2247

8
LI:236680.2:2001JAN12
g2154287
1988
2314

8
LI:236680.2:2001JAN12
g1312625
1444
1937

8
LI:236680.2:2001JAN12
4400655H1
1445
1724

8
LI:236680.2:2001JAN12
g5109483
1451
1887

8
LI:236680.2:2001JAN12
5714792H1
1457
1769

8
LI:236680.2:2001JAN12
6706664H1
1469
1957

8
LI:236680.2:2001JAN12
5429194H1
1469
1757

8
LI:236680.2:2001JAN12
g2229268
1490
1902

8
LI:236680.2:2001JAN12
415958H1
1491
1737

8
LI:236680.2:2001JAN12
6756226H1
1501
2209

8
LI:236680.2:2001JAN12
200080H1
1512
1827

8
LI:236680.2:2001JAN12
200081H1
1512
1828

8
LI:236680.2:2001JAN12
5611292H1
1518
1799

8
LI:236680.2:2001JAN12
g1191362
1524
1680

8
LI:236680.2:2001JAN12
7336684H1
1563
1916

8
LI:236680.2:2001JAN12
2314511H1
1585
1833

8
LI:236680.2:2001JAN12
g6702138
1580
1892

8
LI:236680.2:2001JAN12
g3202284
1583
1896

8
LI:236680.2:2001JAN12
724515R1
1585
2156

8
LI:236680.2:2001JAN12
724515H1
1585
1825

8
LI:236680.2:2001JAN12
g6992823
1589
1892

8
LI:236680.2:2001JAN12
2886039H1
1613
1884

8
LI:236680.2:2001JAN12
2874078H1
1618
1916

8
LI:236680.2:2001JAN12
3702979H1
1619
1916

8
LI:236680.2:2001JAN12
2665478H1
1621
1887

8
LI:236680.2:2001JAN12
2370703H1
1622
1885

8
LI:236680.2:2001JAN12
5913623H1
1623
1931

8
LI:236680.2:2001JAN12
1915623H1
1625
1843

8
LI:236680.2:2001JAN12
5264651H2
1638
1907

8
LI:236680.2:2001JAN12
3825094H1
1645
1890

8
LI:236680.2:2001JAN12
993892T1
1707
1851

8
LI:236680.2:2001JAN12
497542H1
1724
1887

8
LI:236680.2:2001JAN12
g3253828
1725
2161

8
LI:236680.2:2001JAN12
2925528H1
1738
1906

8
LI:236680.2:2001JAN12
2244966H1
1743
1998

8
LI:236680.2:2001JAN12
4320814H1
1748
2035

8
LI:236680.2:2001JAN12
5303358H1
1758
1980

8
LI:236680.2:2001JAN12
3387208H1
1758
1976

8
LI:236680.2:2001JAN12
g2705585
1786
2314

8
LI:236680.2:2001JAN12
g1957960
1801
2285

8
LI:236680.2:2001JAN12
5901612H1
1806
2120

8
LI:236680.2:2001JAN12
1832942H1
1806
2088

8
LI:236680.2:2001JAN12
5894013HI
1806
1916

8
LI:236680.2:2001JAN12
g3433338
2095
2287

8
LI:236680.2:2001JAN12
5067691H1
2096
2326

8
LI:236680.2:2001JAN12
1916921H1
2136
2328

8
LI:236680.2:2001JAN12
2599527T6
2146
2285

8
LI:236680.2:2001JAN12
2560611H1
2169
2322

8
LI:236680.2:2001JAN12
g1241937
2178
2317

8
LI:236680.2:2001JAN12
2330769H1
2255
2326

8
LI:236680.2:2001JAN12
4773732H1
2264
2322

8
LI:236680.2:2001JAN12
g2805069
1417
1903

8
LI:236680.2:2001JAN12
3235380H1
1428
1698

8
LI:236680.2:2001JAN12
571475H1
1440
1661

8
LI:236680.2:2001JAN12
440467H1
1351
1489

8
LI:236680.2:2001JAN12
1948625H1
1353
1613

8
LI:236680.2:2001JAN12
5536452H1
1365
1521

8
LI:236680.2:2001JAN12
056288H1
1363
1535

8
LI:236680.2:2001JAN12
g1810092
1366
1580

8
LI:236680.2:2001JAN12
3486974H1
1370
1635

8
LI:236680.2:2001JAN12
1848282H1
1373
1651

8
LI:236680.2:2001JAN12
6881552H1
1377
1896

8
LI:236680.2:2001JAN12
053537H1
1378
1577

8
LI:236680.2:2001JAN12
413100H1
1380
1595

8
LI:236680.2:2001JAN12
6411776H1
1397
1926

8
LI:236680.2:2001JAN12
5946170H1
1409
1655

8
LI:236680.2:2001JAN12
3557711H1
1351
1632

8
LI:236680.2:2001JAN12
3159474H1
1351
1618

8
LI:236680.2:2001JAN12
4707470H1
1351
1599

8
LI:236680.2:2001JAN12
437494H1
1351
1558

8
LI:236680.2:2001JAN12
g2011273
1351
1541

8
LI:236680.2:2001JAN12
5376179H1
1351
1520

8
LI:236680.2:2001JAN12
g3039383
1312
1674

8
LI:236680.2:2001JAN12
g3429533
1312
1702

8
LI:236680.2:2001JAN12
g3048130
1313
1599

8
LI:236680.2:2001JAN12
1390588H1
1312
1436

8
LI:236680.2:2001JAN12
g1885716
1307
1722

8
LI:236680.2:2001JAN12
2075665H1
1308
1597

8
LI:236680.2:2001JAN12
2293582H1
1308
1585

8
LI:236680.2:2001JAN12
4707390H1
1310
1585

8
LI:236680.2:2001JAN12
4342282H1
1314
1517

8
LI:236680.2:2001JAN12
201900416
1336
1860

8
LI:236680.2:2001JAN12
6076309H1
1336
1598

8
LI:236680.2:2001JAN12
6034056H1
1338
2016

8
LI:236680.2:2001JAN12
g1313848
1346
1841

8
LI:236680.2:2001JAN12
5805420H1
1339
1667

8
LI:236680.2:2001JAN12
2222252H1
1341
1624

8
LI:236680.2:2001JAN12
6040024H1
1346
1986

8
LI:236680.2:2001JAN12
g1921327
1350
1669

8
LI:236680.2:2001JAN12
5854844H1
1346
1644

8
LI:236680.2:2001JAN12
6267478H1
1351
1892

8
LI:236680.2:2001JAN12
4082468H1
1248
1545

8
LI:236680.2:2001JAN12
174345016
1249
1861

8
LI:236680.2:2001JAN12
2101426H1
1253
1534

8
LI:236680.2:2001JAN12
1700062H1
1264
1489

8
LI:236680.2:2001JAN12
1698445H1
1264
1317

8
LI:236680.2:2001JAN12
2955049H1
1265
1515

8
LI:236680.2:2001JAN12
34196716
1267
1861

8
LI:236680.2:2001JAN12
g2107080
1271
1661

8
LI:236680.2:2001JAN12
881668H1
1282
1553

8
LI:236680.2:2001JAN12
g2237266
2000
2323

8
LI:236680.2:2001JAN12
4081922H1
1247
1559

8
LI:236680.2:2001JAN12
3442789H1
2187
2322

8
LI:236680.2:2001JAN12
g2881308
2217
2317

8
LI:236680.2:2001JAN12
4907175H2
2233
2307

8
LI:236680.2:2001JAN12
g1238176
2242
2343

9
LI:228186.1:2001JAN12
2578858F6
3757
4250

9
LI:228186.1:2001JAN12
2578858H1
3757
4017

9
LI:228186.1:2001JAN12
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4181

9
LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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4186

9
LI:228186.1:2001JAN12
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3790
3973

9
LI:228186.1:2001JAN12
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3819
4179

9
LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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3863
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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3903
4180

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LI:228186.1:2001JAN12
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3915
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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3927
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9
LI:228186.1:2001JAN12
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3989
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9
LI:228186.1:2001JAN12
2729487T6
3990
4136

9
LI:228186.1:2001JAN12
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4009
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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4009
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LI:228186.1:2001JAN12
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4017
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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4257
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9
LI:228186.1:2001JAN12
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4266
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9
LI:228186.1:2001JAN12
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4275
4724

9
LI:228186.1:2001JAN12
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4286
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9
LI:228186.1:2001JAN12
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4326
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9
LI:228186.1:2001JAN12
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4326
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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4387
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9
LI:228186.1:2001JAN12
2355972H1
4387
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9
LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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4515
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9
LI:228186.1:2001JAN12
542452T6
4516
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9
LI:228186.1:2001JAN12
542452R6
4516
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9
LI:228186.1:2001JAN12
542452H1
4516
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9
LI:228186.1:2001JAN12
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4521
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9
LI:228186.1:2001JAN12
2355972T6
4524
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9
LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
3905873H1
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9
LI:228186.1:2001JAN12
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5011

9
LI:228186.1:2001JAN12
190176H1
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
917566H1
4648
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9
LI:228186.1:2001JAN12
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4650
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9
LI:228186.1:2001JAN12
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4660
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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3514
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9
LI:228186.1:2001JAN12
2501382H1
3538
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9
LI:228186.1:2001JAN12
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3554
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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3837

9
LI:228186.1:2001JAN12
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3579
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9
LI:228186.1:2001JAN12
3525403H1
3583
3833

9
LI:228186.1:2001JAN12
700438R6
3605
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9
LI:228186.1:2001JAN12
700438H1
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9
LI:228186.1:2001JAN12
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3605
3805

9
LI:228186.1:2001JAN12
700438T6
3605
4140

9
LI:228186.1:2001JAN12
1572292T6
3617
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9
LI:228186.1:2001JAN12
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3617
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9
LI:228186.1:2001JAN12
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3667
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9
LI:228186.1:2001JAN12
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3667
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9
LI:228186.1:2001JAN12
3779008H1
3675
3979

9
LI:228186.1:2001JAN12
5649315H1
3699
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9
LI:228186.1:2001JAN12
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3708
4182

9
LI:228186.1:2001JAN12
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3715
4179

9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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3740
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9
LI:228186.1:2001JAN12
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4181

9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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4179

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LI:228186.1:2001JAN12
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4179

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LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
2937765F6
3008
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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3134
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9
LI:228186.1:2001JAN12
781214H1
1607
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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1716
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9
LI:228186.1:2001JAN12
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1716
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9
LI:228186.1:2001JAN12
3347266H1
2070
2332

9
LI:228186.1:2001JAN12
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2100
2404

9
LI:228186.1:2001JAN12
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2100
2221

9
LI:228186.1:2001JAN12
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2100
2194

9
LI:228186.1:2001JAN12
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2100
2267

9
LI:228186.1:2001JAN12
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2100
2257

9
LI:228186.1:2001JAN12
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2100
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9
LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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2551
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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2839
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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1
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9
LI:228186.1:2001JAN12
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104
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9
LI:228186.1:2001JAN12
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209
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LI:228186.1:2001JAN12
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209
439

9
LI:228186.1:2001JAN12
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294
539

9
LI:228186.1:2001JAN12
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335
888

9
LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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565
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LI:228186.1:2001JAN12
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635
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9
LI:228186.1:2001JAN12
1837462H1
636
890

9
LI:228186.1:2001JAN12
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729
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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1030
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
1837462T6
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
1357315H1
4732
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9
LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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LI:228186.1;2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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3357

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LI:228186.1:2001JAN12
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LI:228186.1:2001JAN12
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3223
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9
LI:228186.1:2001JAN12
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9
LI:228186.1:2001JAN12
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3285
3541

9
LI:228186.1:2001JAN12
5608885H1
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3571

9
LI:228186.1:2001JAN12
5607886H1
3309
3551

10
LI:721233.1:2001JAN12
6271332H2
1
571

10
LI:721233.1:2001JAN12
6271332F8
16
652

10
LI:721233.1:2001JAN12
6271332T8
59
643

11
LI:291759.2:2001JAN12
g1210479
114
173

11
LI:291759.2:2001JAN12
g835196
114
178

11
LI:291759.2:2001JAN12
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117
534

11
LI:291759.2:2001JAN12
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118
405

11
LI:291759.2:2001JAN12
3678854H1
119
196

11
LI:291759.2:2001JAN12
g1314909
125
572

11
LI:291759.2:2001JAN12
309322H1
131
370

11
LI:291759.2:2001JAN12
6456256H1
155
653

11
LI:291759.2:2001JAN12
6456209H1
159
653

11
LI:291759.2:2001JAN12
6456309H1
183
632

11
LI:291759.2:2001JAN12
917190H1
220
551

11
LI:291759.2:2001JAN12
g1753322
250
327

11
LI:291759.2:2001JAN12
2654790T6
277
874

11
LI:291759.2:2001JAN12
4298445H1
291
560

11
LI:291759.2:2001JAN12
7733027H2
552
1131

11
LI:291759.2:2001JAN12
7110866H1
567
654

11
LI:291759.2:2001JAN12
2936830H1
632
906

11
LI:291759.2:2001JAN12
2611540H1
626
680

11
LI:291759.2:2001JAN12
4636570H1
637
891

11
LI:291759.2:2001JAN12
2994056H1
642
920

11
LI:291759.2:2001JAN12
g7043884
652
927

11
LI:291759.2:2001JAN12
g1189956
635
905

11
LI:291752.2:2001JAN12
g3422670
638
904

11
LI:291759.2:2001JAN12
1961123T6
639
869

11
LI:291759.2:2001JAN12
g7318146
646
910

11
LI:291759.2:2001JAN12
2736026T6
646
868

11
LI:291759.2:2001JAN12
g3095265
647
910

11
LI:291759.2:2001JAN12
5759842H1
647
710

11
LI:291759.2:2001JAN12
g1379309
648
910

11
LI:291759.2:2001JAN12
g2278758
648
910

11
LI:291759.2:2001JAN12
1371310H1
649
805

11
LI:291759.2:2001JAN12
g5671213
584
840

11
LI:291759.2:2001JAN12
g2741292
587
846

11
LI:291759.2:2001JAN12
g4988210
587
841

11
LI:291759.2:2001JAN12
g1817486
587
842

11
LI:291759.2:2001JAN12
g7150329
587
837

11
LI:291759.2:2001JAN12
g4998453
587
837

11
LI:291759.2:2001JAN12
g1313377
587
837

11
LI:291759.2:2001JAN12
g1192583
587
837

11
LI:291759.2:2001JAN12
1508944F6
749
1002

11
LI:291759.2:2001JAN12
1508944T6
587
823

11
LI:291759.2:2001JAN12
2738251T6
587
808

11
LI:291759.2:2001JAN12
2519685H1
587
748

11
LI:291759.2:2001JAN12
2860383H1
587
741

11
LI:291759.2:2001JAN12
g5447043
587
840

11
LI:291759.2:2001JAN12
g1379308
587
673

11
LI:291759.2:2001JAN12
6220828H1
587
671

11
LI:291759.2:2001JAN12
1508944H1
587
660

11
LI:291759.2:2001JAN12
g1190150
588
844

11
LI:291759.2:2001JAN12
g1753384
588
839

11
LI:291759.2:2001JAN12
g5741046
587
840

11
LI:291759.2:2001JAN12
g6133239
588
841

11
LI:291759.2:2001JAN12
4533410T1
588
801

11
LI:291759.2:2001JAN12
4533410H1
588
680

11
LI:291759.2:2001JAN12
3809304H1
588
682

11
LI:291759.2:2001JAN12
4128541H1
588
666

11
LI:291759.2:2001JAN12
g4088358
611
866

11
LI:291759.2:2001JAN12
4502947H1
5
255

11
LI:291759.2:2001JAN12
1894293H1
1
203

11
LI:291759.2:2001JAN12
g4124249
1
204

11
LI:291759.2:2001JAN12
1475188H1
1
189

11
LI:291759.2:2001JAN12
1475188T1
1
150

11
LI:291759.2:2001JAN12
1681732F6
814
1007

11
LI:291759.2:2001JAN12
1681732H1
814
1009

11
LI:291759.2:2001JAN12
1681732F7
814
1007

11
LI:291759.2:2001JAN12
910870H1
13
201

11
LI:291759.2:2001JAN12
1681732T7
14
165

11
LI:291759.2:2001JAN12
1681732T6
14
164

11
LI:291759.2:2001JAN12
g2022753
12
197

11
LI:291759.2:2001JAN12
2413084H1
832
1002

11
LI:291759.2:2001JAN12
6883666J1
779
1172

11
LI:291759.2:2001JAN12
1927072H1
1
54

11
LI:291759.2:2001JAN12
g4217544
1
54

11
LI:291759.2:2001JAN12
g1981790
867
1155

11
LI:291759.2:2001JAN12
5298489H1
1
54

11
LI:291759.2:2001JAN12
2671094F6
924
1167

11
LI:291752.2:2001JAN12
2671094T6
924
1438

11
LI:291752.2:2001JAN12
2671094H1
924
1165

11
LI:291752.2:2001JAN12
g1995827
941
1027

11
LI:291759.2:2001JAN12
2736026F6
941
1237

11
LI:291759.2:2001JAN12
2736026H1
941
1070

11
LI:291759.2:2001JAN12
5476134H1
961
1178

11
LI:291759.2:2001JAN12
5477477H1
961
1178

11
LI:291759.2:2001JAN12
5479864H1
961
1229

11
LI:291759.2:2001JAN12
5478264H1
961
1110

11
LI:291759.2:2001JAN12
4692078H1
973
1129

11
LI:291759.2:2001JAN12
g1186868
1013
1173

11
LI:291759.2:2001JAN12
g1186747
1013
1188

11
LI:291759.2:2001JAN12
5103848H1
1029
1245

11
LI:291759.2:2001JAN12
4772463H1
1052
1246

11
LI:291759.2:2001JAN12
1961123H1
1066
1246

11
LI:291759.2:2001JAN12
1961123R6
1066
1246

11
LI:291759.2:2001JAN12
6180072H1
351
643

11
LI:291759.2:2001JAN12
2738251F6
409
936

11
LI:291759.2:2001JAN12
2738251H1
409
674

11
LI:291759.2:2001JAN12
g1860299
413
683

11
LI:291759.2:2001JAN12
3352689H1
421
613

11
LI:291759.2:2001JAN12
g3280105
448
920

11
LI:291759.2:2001JAN12
g5636736
448
915

11
LI:291759.2:2001JAN12
g1243075
450
672

11
LI:291759.2:2001JAN12
2681533H1
433
723

11
LI:291759.2:2001JAN12
g4175465
440
886

11
LI:291759.2:2001JAN12
515771H1
531
669

11
LI:291759.2:2001JAN12
g1997928
1
269

11
LI:291759.2:2001JAN12
7733027J2
16
661

11
LI:291759.2:2001JAN12
g835195
67
392

11
LI:291759.2:2001JAN12
g856172
107
392

11
LI:291759.2:2001JAN12
2654790F6
114
520

11
LI:291759.2:2001JAN12
6883666H1
114
462

11
LI:291759.2:2001JAN12
7597338H1
114
459

11
LI:291759.2:2001JAN12
8194536J1
114
412

11
LI:291759.2:2001JAN12
2328960R6
114
330

11
LI:291759.2:2001JAN12
2654790H1
114
291

11
LI:291759.2:2001JAN12
2328960H1
114
246

11
LI:291759.2:2001JAN12
4996248H1
114
217

11
LI:291759.2:2001JAN12
5610314H1
114
211

11
LI:291759.2:2001JAN12
g856075
114
206

11
LI:291759.2:2001JAN12
7982183H1
1103
1246

11
LI:291759.2:2001JAN12
3475555H1
1116
1270

11
LI:291759.2:2001JAN12
291454H1
1128
1246

11
LI:291759.2:2001JAN12
2009374H1
1168
1246

12
LI:292613.17:2001JAN12
994833R6
1
309

12
LI:292613.17:2001JAN12
994833H1
1
124

12
LI:292613.17:2001JAN12
994833T6
1
363

12
LI:292613.17:2001JAN12
4149665F6
1
355

12
LI:292613.17:2001JAN12
4149665H1
1
228

12
LI:292613.17:2001JAN12
1507329H1
46
170

12
LI:292613.17:2001JAN12
3144082H1
62
276

12
LI:292613.17:2001JAN12
3143359H1
62
224

12
LI:292613.17:2001JAN12
4851779H1
249
508

13
LI:412959.15:2001JAN12
2674048F6
1
330

13
LI:412959.15:2001JAN12
2674048H1
1
211

13
LI:412959.15:2001JAN12
2330307R6
29
493

13
LI:412959.15:2001JAN12
2330307H1
29
304

13
LI:412959.15:2001JAN12
1739552H1
29
95

13
LI:412959.15:2001JAN12
2550691H1
49
290

13
LI:412959.15:2001JAN12
5205237H2
113
370

13
LI:412959.15:2001JAN12
5205237F6
113
406

13
LI:412959.15:2001JAN12
5799259H1
178
406

13
LI:412959.15:2001JAN12
5646172H1
199
293

13
LI:412959.15:2001JAN12
955847H1
325
563

14
LI:482512.3:2001JAN12
g873524
2221
2415

14
LI:482512.3:2001JAN12
g4328019
2156
2401

14
LI:482512.3:2001JAN12
5835727H1
2100
2384

14
LI:482512.3:2001JAN12
g3835121
2159
2400

14
LI:482512.3:2001JAN12
809937R1
2105
2405

14
LI:482512.3:2001JAN12
80993711
2105
2362

14
LI:482512.3:2001JAN12
809937H1
2105
2397

14
LI:482512.3:2001JAN12
g3736000
2108
2405

14
LI:482512.3:2001JAN12
1753767H1
2110
2351

14
LI:482512.3:2001JAN12
1754121H1
2110
2351

14
LI:482512.3:2001JAN12
2371576H1
1856
2086

14
LI:482512.3:2001JAN12
1496803H1
1856
2073

14
LI:482512.3:2001JAN12
4530169H1
1869
2129

14
LI:482512.3:2001JAN12
g2115734
1879
2387

14
LI:482512.3:2001JAN12
8262183J1
1887
2385

14
LI:482512.3:2001JAN12
g2556760
1904
2402

14
LI:482512.3:2001JAN12
g3245066
1905
2405

14
LI:482512.3:2001JAN12
2457752T6
1904
2360

14
LI:482512.3:2001JAN12
g2553409
1907
2401

14
LI:482512.3:2001JAN12
g1718873
1908
2227

14
LI:482512.3:2001JAN12
g1860643
1908
2281

14
LI:482512.3:2001JAN12
g4524169
1915
2400

14
LI:482512.3:2001JAN12
g2115481
1917
2410

14
LI:482512.3:2001JAN12
g3109337
1918
2409

14
LI:482512.3:2001JAN12
g3433865
1925
2402

14
LI:482512.3:2001JAN12
g4196841
1941
2402

14
LI:482512.3:2001JAN12
g4189929
1948
2401

14
LI:482512.3:2001JAN12
g3308018
1952
2405

14
LI:482512.3:2001JAN12
g6131965
1952
2407

14
LI:482512.3:2001JAN12
g4372573
1952
2400

14
LI:482512.3:2001JAN12
6203722H2
1953
2400

14
LI:482512.3:2001JAN12
g6131971
1956
2407

14
LI:482512.3:2001JAN12
g1138274
1966
2400

14
LI:482512.3:2001JAN12
g5632175
1965
2400

14
LI:482512.3:2001JAN12
3602394H1
1965
2250

14
LI:482512.3:2001JAN12
5755635H1
1817
1901

14
LI:482512.3:2001JAN12
5314801H1
1827
2078

14
LI:482512.3:2001JAN12
5314701H1
1827
1985

14
LI:482512.3:2001JAN12
5585639H1
1828
2052

14
LI:482512.3:2001JAN12
5661181H1
1848
2086

14
LI:482512.3:2001JAN12
002115H1
1851
2306

14
LI:482512.3:2001JAN12
3784573H1
1853
2168

14
LI:482512.3:2001JAN12
873570H1
2261
2405

14
LI:482512.3:2001JAN12
4542494H1
2311
2405

14
LI:482512.3:2001JAN12
3075723H1
2326
2400

14
LI:482512.3;2001JAN12
940889H1
2348
2405

14
LI:482512.3:2001JAN12
1380644H1
2019
2283

14
LI:482512.3:2001JAN12
g1148949
2016
2400

14
LI:482512.3:2001JAN12
g1118371
2018
2402

14
LI:482512.3:2001JAN12
1380645H1
2019
2281

14
LI:482512.3:2001JAN12
1384594H1
2019
2260

14
LI:482512.3:2001JAN12
g1421883
2020
2405

14
LI:482512.3:2001JAN12
g1664147
2021
2401

14
LI:482512.3:2001JAN12
945748H1
2023
2185

14
LI:482512.3:2001JAN12
3839205H1
2024
2339

14
LI:482512.3:2001JAN12
g3178370
2026
2411

14
LI:482512.3:2001JAN12
g1398466
1981
2404

14
LI:482512.3:2001JAN12
5663784H1
1984
2274

14
LI:482512.3:2001JAN12
g2618247
1995
2401

14
LI:482512.3:2001JAN12
g2834644
1995
2401

14
LI:482512.3:2001JAN12
g1754374
1996
2404

14
LI:482512.3:2001JAN12
g3246099
1999
2410

14
LI:482512.3:2001JAN12
g4107748
2000
2401

14
LI:482512.3:2001JAN12
g1718874
2002
2402

14
LI:482512.3:2001JAN12
g1861028
2004
2402

14
LI:482512.3:2001JAN12
g1955011
2009
2378

14
LI:482512.3:2001JAN12
2017265H1
2015
2160

14
LI:482512.3:2001JAN12
g927843
1487
1645

14
LI:482512.3:2001JAN12
3944613H1
1490
1645

14
LI:482512.3:2001JAN12
g1057615
1490
1632

14
LI:482512.3:2001JAN12
g711667
1496
1653

14
LI:482512.3:2001JAN12
g763648
1497
1598

14
LI:482512.3:2001JAN12
5699665H1
1500
1675

14
LI:482512.3:2001JAN12
g2714398
1504
1653

14
LI:482512.3:2001JAN12
g668934
1505
1598

14
LI:482512.3:2001JAN12
2456911H1
1531
1598

14
LI:482512.3:2001JAN12
g3146519
1534
1598

14
LI:482512.3:2001JAN12
g709509
1536
1598

14
LI:482512.3:2001JAN12
1384064H1
1579
1645

14
LI:482512.3:2001JAN12
6559028H1
1813
2383

14
LI:482512.3:2001JAN12
g1146774
1812
2174

14
LI:482512.3:2001JAN12
1518980T7
1816
2309

14
LI:482512.3:2001JAN12
6949010H1
1817
2288

14
LI:482512.3:2001JAN12
2325041H1
1817
1948

14
LI:482512.3:2001JAN12
5755636H1
1816
2045

14
LI:482512.3:2001JAN12
1855715F6
1817
2110

14
LI:482512.3:2001JAN12
5263754H1
1817
2051

14
LI:482512.3:2001JAN12
1855715H1
1817
1879

14
LI:482512.3:2001JAN12
g3277379
1429
1598

14
LI:482512.3:2001JAN12
6948396H1
1433
1566

14
LI:482512.3:2001JAN12
g2754313
1438
1598

14
LI:482512.3:2001JAN12
g3659102
1441
1653

14
LI:482512.3:2001JAN12
2544736H1
1441
1639

14
LI:482512.3:2001JAN12
2761382H1
1442
1667

14
LI:482512.3:2001JAN12
g2714655
1441
1645

14
LI:482512.3:2001JAN12
g3802581
1446
1631

14
LI:482512.3:2001JAN12
1991282H1
1447
1639

14
LI:482512.3:2001JAN12
g985287
1447
1598

14
LI:482512.3:2001JAN12
6700167H1
1451
1892

14
LI:482512.3:2001JAN12
6558151H1
1453
1975

14
LI:482512.3:2001JAN12
g1042434
1452
1598

14
LI:482512.3:2001JAN12
g747038
1457
1645

14
LI:482512.3:2001JAN12
4638167H1
1462
1644

14
LI:482512.3:2001JAN12
3810276H1
1480
1598

14
LI:482512.3:2001JAN12
g1383051
1485
1645

14
LI:482512.3:2001JAN12
g2713364
1484
1613

14
LI:482512.3:2001JAN12
g2593948
2164
2327

14
LI:482512.3:2001JAN12
g1625916
1980
2401

14
LI:482512.3:2001JAN12
g2742370
2191
2405

14
LI:482512.3:2001JAN12
2503846H1
2201
2400

14
LI:482512.3:2001JAN12
g1550293
938
1029

14
LI:482512.3:2001JAN12
g873523
940
1267

14
LI:482512.3:2001JAN12
g875484
940
1278

14
LI:482512.3:2001JAN12
3140312H1
940
1217

14
LI:482512.3:2001JAN12
046678H1
962
1243

14
LI:482512.3:2001JAN12
043864H1
963
1277

14
LI:482512.3:2001JAN12
1916774H1
974
1277

14
LI:482512.3:2001JAN12
g1392105
980
1489

14
LI:482512.3:2001JAN12
g1685835
982
1387

14
LI:482512.3:2001JAN12
4155543H1
1006
1254

14
LI:482512.3:2001JAN12
6951737H1
1007
1244

14
LI:482512.3:2001JAN12
3844826H1
1014
1320

14
LI:482512.3:2001JAN12
3257104H1
1036
1316

14
LI:482512.3:2001JAN12
3979735H1
1047
1361

14
LI:482512.3:2001JAN12
5068828H1
1048
1348

14
LI:482512.3:2001JAN12
g675099
1061
1479

14
LI:482512.3:2001JAN12
g706514
1061
1458

14
LI:482512.3:2001JAN12
2185344H1
1075
1386

14
LI:482512.3:2001JAN12
589365H1
1075
1335

14
LI:482512.3:2001JAN12
5031411H1
1076
1375

14
LI:482512.3:2001JAN12
4087425H1
1086
1394

14
LI:482512.3:2001JAN12
g2433835
1102
1526

14
LI:482512.3:2001JAN12
7244978H1
1115
1673

14
LI:482512.3:2001JAN12
045891H1
1119
1388

14
LI:482512.3:2001JAN12
5260860H1
1119
1369

14
LI:482512.3:2001JAN12
1305950T6
1120
1631

14
LI:482512.3:2001JAN12
4624991H1
1121
1390

14
LI:482512.3:2001JAN12
3516303H1
1125
1398

14
LI:482512.3:2001JAN12
306079H1
1139
1363

14
LI:482512.3:2001JAN12
307499H1
1140
1524

14
LI:482512.3:2001JAN12
g5110580
1143
1515

14
LI:482512.3:2001JAN12
5962610H1
1170
1657

14
LI:482512.3:2001JAN12
7232448H1
1168
1598

14
LI:482512.3:2001JAN12
5974019H1
1189
1645

14
LI:482512.3:2001JAN12
4626361H1
1189
1460

14
LI:482512.3:2001JAN12
4637075H1
1195
1460

14
LI:482512.3:2001JAN12
6977977H1
1214
1632

14
LI:482512.3:2001JAN12
6726370H1
1215
1598

14
LI:482512.3:2001JAN12
6820986H1
1223
1598

14
LI:482512.3:2001JAN12
2182014H1
1230
1517

14
LI:482512.3:2001JAN12
6559637H1
1248
1598

14
LI:482512.3:2001JAN12
4974150H1
1257
1548

14
LI:482512.3:2001JAN12
1384882H1
1266
1480

14
LI:482512.3:2001JAN12
4109127H1
1282
1467

14
LI:482512.3:2001JAN12
3905520H1
1287
1479

14
LI:482512.3:2001JAN12
1296488F1
1293
1598

14
LI:482512.3:2001JAN12
1296488H1
1293
1520

14
LI:482512.3:2001JAN12
2841257H1
1304
1576

14
LI:482512.3:2001JAN12
1257539H1
1313
1468

14
LI:482512.3:2001JAN12
g2837530
1324
1598

14
LI:482512.3:2001JAN12
g1576401
1326
1645

14
LI:482512.3:2001JAN12
g2018016
1330
1631

14
LI:482512.3:2001JAN12
g4389755
1332
1598

14
LI:482512.3:2001JAN12
2364653H1
1341
1591

14
LI:482512.3:2001JAN12
2825595H1
1341
1561

14
LI:482512.3:2001JAN12
g1550340
1360
1598

14
LI:482512.3:2001JAN12
g2556753
1368
1653

14
LI:482512.3:2001JAN12
g3425443
1377
1598

14
LI:482512.3:2001JAN12
g1392159
1377
1598

14
LI:482512.3:2001JAN12
4638729H1
1388
1650

14
LI:482512.3:2001JAN12
2707566H1
1395
1661

14
LI:482512.3:2001JAN12
1990815T6
1395
1631

14
LI:482512.3:2001JAN12
4182102H1
1399
1639

14
LI:482512.3:2001JAN12
g1736048
1401
1598

14
LI:482512.3:2001JAN12
3414387H1
1405
1638

14
LI:482512.3:2001JAN12
3618923H1
1407
1686

14
LI:482512.3:2001JAN12
g1550465
1407
1644

14
LI:482512.3:2001JAN12
3618907H1
1406
1639

14
LI:482512.3:2001JAN12
g2219112
1408
1598

14
LI:482512.3:2001JAN12
g880239
1420
1598

14
LI:482512.3:2001JAN12
g717966
1426
1645

14
LI:482512.3:2001JAN12
4557378H1
1424
1639

14
LI:482512.3:2001JAN12
g3277736
1427
1515

14
LI:482512.3:2001JAN12
g991594
1428
1646

14
LI:482512.3:2001JAN12
g696806
828
1200

14
LI:482512.3:2001JAN12
7333420H1
842
1480

14
LI:482512.3:2001JAN12
6173218H1
845
1162

14
LI:482512.3:2001JAN12
g1151824
849
1344

14
LI:482512.3:2001JAN12
2400804H1
861
1113

14
LI:482512.3:2001JAN12
g763702
873
1148

14
LI:482512.3:2001JAN12
1894128H1
877
1121

14
LI:482512.3:2001JAN12
2401675H1
877
1118

14
LI:482512.3:2001JAN12
4718965H1
885
1163

14
LI:482512.3:2001JAN12
g1550279
903
1047

14
LI:482512.3:2001JAN12
085340H1
926
1215

14
LI:482512.3:2001JAN12
g1025090
2171
2399

14
LI:482512.3:2001JAN12
g690874
2166
2399

14
LI:482512.3:2001JAN12
g2277764
2205
2405

14
LI:482512.3:2001JAN12
5187711H1
2173
2407

14
LI:482512.3:2001JAN12
g690873
2174
2401

14
LI:482512.3:2001JAN12
g3329866
2177
2372

14
LI:482512.3:2001JAN12
5371978H1
798
1032

14
LI:482512.3:2001JAN12
g1057614
801
1183

14
LI:482512.3:2001JAN12
5302479H1
806
1041

14
LI:482512.3:2001JAN12
g985513
802
1126

14
LI:482512.3:2001JAN12
g1472689
802
1029

14
LI:482512.3:2001JAN12
g1966605
806
1072

14
LI:482512.3:2001JAN12
046056H1
815
1121

14
LI:482512.3:2001JAN12
2050472H1
816
1089

14
LI:482512.3:2001JAN12
4530227H1
818
1047

14
LI:482512.3:2001JAN12
6557789H1
817
1438

14
LI:482512.3:2001JAN12
g711812
825
1048

14
LI:482512.3:2001JAN12
g927924
825
1154

14
LI:482512.3:2001JAN12
g747138
825
1091

14
LI:482512.3:2001JAN12
2230315H1
27
308

14
LI:482512.3:2001JAN12
8175222H1
31
482

14
LI:482512.3:2001JAN12
5014968H1
31
273

14
LI:482512.3:2001JAN12
g880294
31
322

14
LI:482512.3:2001JAN12
g710258
31
263

14
LI:482512.3:2001JAN12
6913395J1
30
124

14
LI:482512.3:2001JAN12
g2661035
31
1598

14
LI:482512.3:2001JAN12
2457752F6
31
426

14
LI:482512.3:2001JAN12
1804835F6
31
350

14
LI:482512.3:2001JAN12
g764891
31
309

14
LI:482512.3:2001JAN12
2367452H1
31
253

14
LI:482512.3:2001JAN12
2214947H1
31
237

14
LI:482512.3:2001JAN12
1804835H1
31
226

14
LI:482512.3:2001JAN12
g672934
31
231

14
LI:482512.3:2001JAN12
3759832H1
31
218

14
LI:482512.3:2001JAN12
2457752H1
31
170

14
LI:482512.3:2001JAN12
g669457
31
132

14
LI:482512.3:2001JAN12
1321111H1
45
298

14
LI:482512.3:2001JAN12
046743H1
48
346

14
LI:482512.3:2001JAN12
2958213H1
53
172

14
LI:482512.3:2001JAN12
041586H1
57
372

14
LI:482512.3:2001JAN12
g1995825
62
359

14
LI:482512.3:2001JAN12
021288H1
71
355

14
LI:482512.3:2001JAN12
023125H1
70
290

14
LI:482512.3:2001JAN12
020669H1
71
391

14
LI:482512.3:2001JAN12
023365H1
71
400

14
LI:482512.3:2001JAN12
023083H1
71
261

14
LI:482512.3:2001JAN12
046013H1
71
350

14
LI:482512.3:2001JAN12
045282H1
75
443

14
LI:482512.3:2001JAN12
023015H1
71
284

14
LI:482512.3:2001JAN12
g2219111
80
206

14
LI:482512.3:2001JAN12
5057178H1
120
394

14
LI:482512.3:2001JAN12
6505740H1
159
729

14
LI:482512.3:2001JAN12
4530837H1
157
440

14
LI:482512.3:2001JAN12
4365205H1
191
480

14
LI:482512.3:2001JAN12
g6837967
196
686

14
LI:482512.3:2001JAN12
4979543H1
198
487

14
LI:482512.3:2001JAN12
532837H1
198
319

14
LI:482512.3:2001JAN12
g4891444
219
682

14
LI:482512.3:2001JAN12
3386615H1
362
518

14
LI:482512.3:2001JAN12
1990815H1
368
542

14
LI:482512.3:2001JAN12
1305950F6
404
872

14
LI:482512.3:2001JAN12
1305950H1
404
642

14
LI:482512.3:2001JAN12
3783350H1
408
691

14
LI:482512.3:2001JAN12
2962868H1
424
726

14
LI:482512.3:2001JAN12
4528095H1
453
714

14
LI:482512.3:2001JAN12
8187102H1
454
1037

14
LI:482512.3:2001JAN12
1855017H1
492
783

14
LI:482512.3:2001JAN12
g1576448
508
845

14
LI:482512.3:2001JAN12
g1471254
548
916

14
LI:482512.3:2001JAN12
045976H1
551
787

14
LI:482512.3:2001JAN12
6134930H1
577
911

14
LI:482512.3:2001JAN12
4972696H1
577
871

14
LI:482512.3:2001JAN12
g1959676
581
1009

14
LI:482512.3:2001JAN12
5743902H1
582
663

14
LI:482512.3:2001JAN12
491086H1
591
950

14
LI:482512.3:2001JAN12
6913395H1
613
1070

14
LI:482512.3:2001JAN12
4821459H1
603
905

14
LI:482512.3:2001JAN12
3323541H2
605
832

14
LI:482512.3:2001JAN12
g1626259
616
998

14
LI:482512.3:2001JAN12
g1024977
614
964

14
LI:482512.3:2001JAN12
2111581H1
614
880

14
LI:482512.3:2001JAN12
g1626020
616
1009

14
LI:482512.3:2001JAN12
g2026440
625
937

14
LI:482512.3:2001JAN12
5680821H1
636
926

14
LI:482512.3:2001JAN12
6909290H1
644
1232

14
LI:482512.3:2001JAN12
4595758H1
685
964

14
LI:482512.3:2001JAN12
4313975H1
687
975

14
LI:482512.3:2001JAN12
4960424H1
690
982

14
LI:482512.3:2001JAN12
4784119H1
691
946

14
LI:482512.3:2001JAN12
6743028H1
692
1235

14
LI:482512.3:2001JAN12
g1157878
704
1025

14
LI:482512.3:2001JAN12
2559233H1
722
1003

14
LI:482512.3:2001JAN12
g1971698
728
1051

14
LI:482512.3:2001JAN12
5390379H1
731
1017

14
LI:482512.3:2001JAN12
3515683H1
733
970

14
LI:482512.3:2001JAN12
1870164H1
738
1028

14
LI:482512.3:2001JAN12
1871314H1
738
1038

14
LI:482512.3:2001JAN12
g1386366
743
1241

14
LI:482512.3:2001JAN12
2459470H1
760
983

14
LI:482512.3:2001JAN12
5685572H1
775
1050

14
LI:482512.3:2001JAN12
6916088H1
784
1431

14
LI:482512.3:2001JAN12
g718055
789
1198

14
LI:482512.3:2001JAN12
7346763H1
2032
2417

14
LI:482512.3:2001JAN12
g1626212
2033
2400

14
LI:482512.3:2001JAN12
1855715T6
2036
2356

14
LI:482512.3:2001JAN12
g3835444
2041
2403

14
LI:482512.3:2001JAN12
466696H1
2057
2289

14
LI:482512.3:2001JAN12
g5864949
2065
2400

14
LI:482512.3:2001JAN12
g875485
2073
2414

14
LI:482512.3:2001JAN12
2301339H1
2075
2327

14
LI:482512.3:2001JAN12
g674340
2080
2407

14
LI:482512.3:2001JAN12
g682338
2092
2400

14
LI:482512.3:2001JAN12
g1140444
2095
2407

14
LI:482512.3:2001JAN12
g6196222
2098
2401

14
LI:482512.3:2001JAN12
g1685729
2098
2405

14
LI:482512.3:2001JAN12
g5638155
2099
2400

14
LI:482512.3:2001JAN12
g4268508
2099
2400

14
LI:482512.3:2001JAN12
g4006452
2101
2405

14
LI:482512.3:2001JAN12
g3330360
2225
2400

14
LI:482512.3:2001JAN12
2009751H1
2234
2400

14
LI:482512.3:2001JAN12
g1136823
2227
2400

14
LI:482512.3:2001JAN12
g2195197
2256
2405

14
LI:482512.3:2001JAN12
873570T1
2260
2368

14
LI:482512.3:2001JAN12
6815272J1
1
297

14
LI:482512.3:2001JAN12
6815272R8
1
290

14
LI:482512.3:2001JAN12
g981955
1
298

14
LI:482512.3:2001JAN12
6549283H1
17
572

14
LI:482512.3:2001JAN12
7623377H1
24
642

14
LI:482512.3:2001JAN12
g2009082
25
326

14
LI:482512.3:2001JAN12
1949217H1
25
289

15
LI:413231.6:2001JAN12
2424460H1
1
199

15
LI:413231.6:2001JANJ2
1706344F6
1
569

15
LI:413231.6:2001JAN12
1706344H1
1
233

15
LI:413231.6:2001JAN12
7337667H1
162
796

15
LI:413231.6:2001JAN12
1237075H1
408
662

15
LI:413231.6:2001JAN12
8271572T1
472
811

15
LI:413231.6:2001JAN12
1706344T6
503
954

15
LI:413231.6:2001JAN12
g7276320
701
996

16
LI:203383.1:2001JAN12
g2819701
975
1227

16
LI:203383.1:2001JAN12
5323709T6
800
1208

16
LI:203383.1:2001JAN12
5323709F6
629
1116

16
LI:203383.1:2001JAN12
6537415H1
479
1062

16
LI:203383.1:2001JAN12
2158630H1
828
1053

16
LI:203383.1:2001JAN12
5711628H1
749
1026

16
LI:203383.1:2001JAN12
1296562H1
740
959

16
LI:203383.1:2001JAN12
5483082H1
629
909

16
LI:203383.1:2001JAN12
5477880H1
629
893

16
LI;203383.1:2001JAN12
5323709H1
629
890

16
LI:203383.1:2001JAN12
5322729H1
629
879

16
LI:203383.1:2001JAN12
6214988H1
1
561

16
LI:203383.1:2001JAN12
g2902159
834
1228

16
LI:203383.1:2001JAN12
g7281445
1036
1228

16
LI:203383.1:2001JAN12
g2000936
950
1228

16
LI:203383.1:2001JAN12
g4188363
859
1228

16
LI:203383.1:2001JAN12
g2819715
965
1242

16
LI:203383.1:2001JAN12
g4244517
914
1234

16
LI:203383.1:2001JAN12
g4738989
964
1234

16
LI:203383.1:2001JAN12
g5878892
763
1233

16
LI:203383.1:2001JAN12
g2732240
764
1232

17
LI:133186.4:2001JAN12
7688030J1
1
577

17
LI:133186.4:2001JAN12
7581594H1
98
577

17
LI:133186.4:2001JAN12
7956839H1
111
577

17
LI:133186.4:2001JAN12
71603710V1
98
543

18
LI:238576.2:2001JAN12
4382965H1
346
613

18
LI:238576.2:2001JAN12
g1983225
349
712

18
LI:238576.2:2001JAN12
6099077H1
259
387

18
LI:238576.2:2001JAN12
6564603H1
264
850

18
LI:238576.2:2001JAN12
6140937H1
261
498

18
LI:238576.2:2001JAN12
7053558H1
264
904

18
LI:238576.2:2001JAN12
7001622H1
263
771

18
LI:238576.2:2001JAN12
6137522H1
265
558

18
LI:238576.2:2001JAN12
71300749V1
280
946

18
LI:238576.2:2001JAN12
4637090H1
296
554

18
LI:238576.2:2001JAN12
6059510H1
307
878

18
LI:238576.2:2001JAN12
6424708H1
307
865

18
LI:238576.2:2001JAN12
4943507H1
307
603

18
LI:238576.2:2001JAN12
5107771H1
308
557

18
LI:238576.2:2001JAN12
6858201H1
316
637

18
LI:238576.2:2001JAN12
5574827H1
324
593

18
LI:238576.2:2001JAN12
5292641H2
332
511

18
LI:238576.2:2001JAN12
7351314H1
334
785

18
LI:238576.2:2001JAN12
3126908H1
334
622

18
LI:238576.2:2001JAN12
2913933H1
334
609

18
LI:238576.2:2001JAN12
4530958H1
338
626

18
LI:238576.2:2001JAN12
595195H1
337
535

18
LI:238576.2:2001JAN12
7272621H1
338
863

18
LI:238576.2:2001JAN12
2899931H1
346
652

18
LI:238576.2:2001JAN12
6120217H1
260
838

18
LI:238576.2:2001JAN12
5118272H1
259
532

18
LI:238576.2:2001JAN12
3984701H1
186
494

18
LI:238576.2:2001JAN12
3642338H1
184
497

18
LI:238576.2:2001JAN12
3209133H1
184
419

18
LI:238576.2:2001JAN12
3384510H1
185
454

18
LI:238576.2:2001JAN12
2690213H1
185
444

18
LI:238576.2:2001JAN12
5338826H1
185
293

18
LI:238576.2:2001JAN12
7231614H1
186
732

18
LI:238576.2:2001JAN12
5076156H1
189
466

18
LI:238576.2:2001JAN12
5265030H1
192
453

18
LI:238576.2:2001JAN12
5351009H1
190
298

18
LI:238576.2:2001JAN12
4056963H1
190
509

18
LI:238576.2:2001JAN12
3128195H1
190
484

18
LI:238576.2:2001JAN12
2562930H2
190
453

18
LI:238576.2:2001JAN12
1581592H1
190
394

18
LI:238576.2:2001JAN12
100567H1
190
409

18
LI:238576.2:2001JAN12
71152815V1
185
850

18
LI:238576.2:2001JAN12
3416969H1
192
455

18
LI:238576.2:2001JAN12
974491H1
194
352

18
LI:238576.2:2001JAN12
6126528H1
228
544

18
LI:238576.2:2001JAN12
7027657H1
198
632

18
LI:238576.2:2001JAN12
2198232H1
199
464

18
LI:238576.2:2001JAN12
6168044H1
199
321

18
LI:238576.2:2001JAN12
4563346H1
199
453

18
LI:238576.2:2001JAN12
6118740F8
213
832

18
LI:238576.2:2001JAN12
265346H1
201
557

18
LI:238576.2:2001JAN12
3163862H1
201
493

18
LI:238576.2:2001JAN12
3199104H1
205
338

18
LI:238576.2:2001JAN12
5196915H1
205
478

18
LI:238576.2:2001JAN12
60123995D2
205
415

18
LI:238576.2:2001JAN12
4790072H1
207
491

18
LI:238576.2:2001JAN12
4549532H1
209
489

18
LI:238576.2:2001JAN12
3316908H1
210
468

18
LI:238576.2:2001JAN12
935927H1
210
437

18
LI:238576.2:2001JAN12
3928681H1
211
497

18
LI:238576.2:2001JAN12
2057892H1
210
469

18
LI:238576.2:2001JAN12
6161637H1
211
530

18
LI:238576.2:2001JAN12
139725H1
213
277

18
LI:238576.2:2001JAN12
139726H1
213
281

18
LI:238576.2:2001JAN12
5687728H1
216
497

18
LI:238576.2:2001JAN12
4997133F6
220
713

18
LI:238576.2:2001JAN12
3217567H1
219
521

18
LI:238576.2:2001JAN12
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219
514

18
LI:238576.2:2001JAN12
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220
475

18
LI:238576.2:2001JAN12
3900367H1
221
500

18
LI:238576.2:2001JAN12
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222
500

18
LI:238576.2:2001JAN12
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220
410

18
LI:238576.2:2001JAN12
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223
498

18
LI:238576.2:2001JAN12
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223
553

18
LI:238576.2:2001JAN12
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226
529

18
LI:238576.2:2001JAN12
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226
521

18
LI:238576.2:2001JAN12
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227
454

18
LI:238576.2:2001JAN12
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226
524

18
LI:238576.2:2001JAN12
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228
479

18
LI:238576.2:2001JAN12
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235
504

18
LI:238576.2:2001JAN12
3454496H2
240
506

18
LI:238576.2:2001JAN12
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243
518

18
LI:238576.2:2001JAN12
4212591H1
243
517

18
LI:238576.2:2001JAN12
6329103H1
244
828

18
LI:238576.2:2001JAN12
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243
765

18
LI:238576.2:2001JAN12
4668415H1
243
525

18
LI:238576.2:2001JAN12
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243
531

18
LI:238576.2:2001JAN12
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244
478

18
LI:238576.2:2001JAN12
1932192H1
245
521

18
LI:238576.2:2001JAN12
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246
483

18
LI:238576.2:2001JAN12
6563713H1
247
702

18
LI:238576.2:2001JAN12
6902103H1
250
869

18
LI:238576.2:2001JAN12
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248
530

18
LI:238576.2:2001JAN12
134194R1
256
729

18
LI:238576.2:2001JAN12
5812769H1
253
556

18
LI:238576.2:2001JAN12
3539319H1
256
442

18
LI:238576.2:2001JAN12
134194H1
257
420

18
LI:238576.2:2001JAN12
134194R6
257
863

18
LI:238576.2:2001JAN12
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151
420

18
LI:238576.2:2001JAN12
3616603H1
152
364

18
LI:238576.2:2001JAN12
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156
396

18
LI:238576.2:2001JAN12
5762340H1
159
693

18
LI:238576.2:2001JAN12
3320288H1
161
435

18
LI:238576.2:2001JAN12
3320240H1
160
437

18
LI:238576.2:2001JAN12
g1981931
163
537

18
LI:238576.2:2001JAN12
3320841H1
167
443

18
LI:238576.2:2001JAN12
6286430H2
170
785

18
LI:238576.2:2001JAN12
6539558H1
170
727

18
LI:238576.2:2001JAN12
4069509H1
170
483

18
LI:238576.2:2001JAN12
2846475H1
170
443

18
LI:238576.2:2001JAN12
g5665303
171
641

18
LI:238576.2:2001JAN12
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170
486

18
LI:238576.2:2001JAN12
2515442H1
177
519

18
LI:238576.2:2001JAN12
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177
430

18
LI:238576.2:2001JAN12
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176
390

18
LI:238576.2:2001JAN12
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176
350

18
LI:238576.2:2001JAN12
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179
460

18
LI:238576.2:2001JAN12
2863756H1
179
509

18
LI:238576.2:2001JAN12
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181
428

18
LI:238576.2:2001JAN12
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184
471

18
LI:238576.2:2001JAN12
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182
453

18
LI:238576.2:2001JAN12
4445516H1
181
454

18
LI:238576.2:2001JAN12
5646947H1
182
422

18
LI:238576.2:2001JAN12
6252033H1
857
1271

18
LI:238576.2:2001JAN12
g2741102
858
1333

18
LI:238576.2:2001JAN12
6252420H1
862
1333

18
LI:238576.2:2001JAN12
3999837H1
863
1170

18
LI:238576.2:2001JAN12
4656292H1
863
1151

18
LI:238576.2:2001JAN12
g4533809
868
1334

18
LI:238576.2:2001JAN12
2698233W
871
1113

18
LI:238576.2:2001JAN12
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872
1333

18
LI:238576.2:2001JAN12
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872
1333

18
LI:238576.2:2001JAN12
g4899785
872
1333

18
LI:238576.2:2001JAN12
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869
1204

18
LI:238576.2:2001JAN12
5559592H1
825
1111

18
LI:238576.2:2001JAN12
6860869H1
836
1349

18
LI:238576.2:2001JAN12
535566H1
830
1118

18
LI:238576.2:2001JAN12
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832
1337

18
LI:238576.2:2001JAN12
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829
1342

18
LI:238576.2:2001JAN12
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1334

18
LI:238576.2:2001JAN12
g3884780
866
1336

18
LI:238576.2:2001JAN12
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841
1333

18
LI:238576.2:2001JAN12
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849
1338

18
LI:238576.2:2001JAN12
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849
1188

18
LI:238576.2:2001JAN12
5638395H1
849
1112

18
LI:238576.2:2001JAN12
1259213F1
854
1195

18
LI:238576.2:2001JAN12
1259213H1
854
1124

18
LI:238576.2:2001JAN12
6480833H1
1
439

18
LI:238576.2:2001JAN12
4753971H1
94
355

18
LI:238576.2:2001JAN12
5780889T6
104
682

18
LI:238576.2:2001JAN12
3854966H1
127
241

18
LI:238576.2:2001JAN12
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140
292

18
LI:238576.2:2001JAN12
3673616H1
140
450

18
LI:238576.2:2001JAN12
1298467H1
140
393

18
LI:238576.2:2001JAN12
8174823H1
143
802

18
LI:238576.2:2001JAN12
161642H1
148
248

18
LI:238576.2:2001JAN12
g5657944
919
1333

18
LI:238576.2:2001JAN12
g2017125
922
1157

18
LI:238576.2:2001JAN12
g1801517
922
1337

18
LI:238576.2:2001JAN12
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924
1350

18
LI:238576.2:2001JAN12
7332139H1
931
1340

18
LI:238576.2:2001JAN12
71151083V1
929
1343

18
LI:238576.2:2001JAN12
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930
1297

18
LI:238576.2:2001JAN12
6847334H1
943
1326

18
LI:238576.2:2001JAN12
2314966H1
934
1238

18
LI:238576.2:2001JAN12
g2270407
935
1092

18
LI:238576.2:2001JAN12
2314982H1
948
1234

18
LI:238576.2:2001JAN12
501348H1
946
1121

18
LI:238576.2:2001JAN12
501349R6
946
1344

18
LI:238576.2:2001JAN12
501349T6
946
1293

18
LI:238576.2:2001JAN12
3779876H1
947
1274

18
LI:238576.2:2001JAN12
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953
1333

18
LI:238576.2:2001JAN12
g5848253
954
1338

18
LI:238576.2:2001JAN12
406979H1
956
1213

18
LI:238576.2:2001JAN12
2684534H1
964
1221

18
LI:238576.2:2001JAN12
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969
1336

18
LI:238576.2:2001JAN12
g3118693
969
1340

18
LI:238576.2:2001JAN12
5030434H1
964
1217

18
LI:238576.2:2001JAN12
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970
1333

18
LI:238576.2:2001JAN12
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975
1333

18
LI:238576.2:2001JAN12
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976
1333

18
LI:238576.2:2001JAN12
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976
1336

18
LI:238576.2:2001JAN12
g3802778
976
1336

18
LI:238576.2:2001JAN12
2564348H1
984
1267

18
LI:238576.2:2001JAN12
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990
1333

18
LI:238576.2:2001JAN12
g2751136
990
1326

18
LI:238576.2:2001JAN12
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996
1333

18
LI:238576.2:2001JAN12
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1000
1312

18
LI:238576.2:2001JAN12
6847534H1
1006
1326

18
LI:238576.2:2001JAN12
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1014
1333

18
LI:238576.2:2001JAN12
627744H1
1016
1287

18
LI:238576.2:2001JAN12
1840346H1
1020
1290

18
LI:238576.2:2001JAN12
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1033
1333

18
LI:238576.2:2001JAN12
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1034
1332

18
LI:238576.2:2001JAN12
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1034
1321

18
LI:238576.2:2001JAN12
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1034
1299

18
LI:238576.2:2001JAN12
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18
LI:238576.2:2001JAN12
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1037
1333

18
LI:238576.2:2001JAN12
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1336

18
LI:238576.2:2001JAN12
6555494H1
1055
1333

18
LI:238576.2:2001JAN12
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1050
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18
LI:238576.2:2001JAN12
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1327

18
LI:238576.2:2001JAN12
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1051
1336

18
LI:238576.2:2001JAN12
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1061
1335

18
LI:238576.2:2001JAN12
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18
LI:238576.2:2001JAN12
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1074
1336

18
LI:238576.2:2001JAN12
5989860H1
1076
1330

18
LI:238576.2:2001JAN12
6395065H1
1080
1328

18
LI:238576.2;2001JAN12
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1085
1336

18
LI:238576.2:2001JAN12
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1085
1335

18
LI:238576.2:2001JAN12
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1085
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18
LI:238576.2:2001JAN12
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18
LI:238576.2:2001JAN12
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1087
1275

18
LI:238576.2:2001JAN12
6353879H1
1088
1325

18
LI:238576.2:2001JAN12
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1095
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18
LI:238576.2:2001JAN12
2558418H1
1128
1333

18
LI:238576.2;2001JAN12
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1133
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18
LI:238576.2:2001JAN12
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1142
1338

18
LI:238576.2:2001JAN12
1925508R6
1143
1333

18
LI:238576.2:2001JAN12
1925508H1
1143
1333

18
LI:238576.2:2001JAN12
g5529626
1157
1333

18
LI:238576.2:2001JAN12
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884
1088

18
LI:238576.2:2001JAN12
g5450857
874
1335

18
LI:238576.2:2001JAN12
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876
1335

18
LI:238576.2:2001JAN12
g3665665
880
1333

18
LI:238576.2:2001JAN12
4599219H1
875
1188

18
LI:238576.2:2001JAN12
227744R1
884
1335

18
LI:238576.2:2001JAN12
g5885583
885
1335

18
LI:238576.2:2001JAN12
371585H1
882
1124

18
LI:238576.2:2001JAN12
g2325594
886
1333

18
LI:238576.2:2001JAN12
g2195406
894
1332

18
LI:238576.2:2001JAN12
g4664967
897
1333

18
LI:238576.2:2001JAN12
g2674662
905
1335

18
LI:238576.2:2001JAN12
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906
1336

18
LI:238576.2:2001JAN12
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907
1333

18
LI:238576.2:2001JAN12
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909
1333

18
LI:238576.2:2001JAN12
70942171V1
909
1079

18
LI:238576.2:2001JAN12
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910
1333

18
LI:238576.2:2001JAN12
g2458743
916
1336

18
LI:238576.2:2001JAN12
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918
1316

18
LI:238576.2:2001JAN12
3728404H1
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1346

18
LI:238576.2:2001JAN12
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1168
1336

18
LI:238576.2:2001JAN12
235645H1
1183
1333

18
LI:238576.2:2001JAN12
236139H1
1183
1333

18
LI:238576.2:2001JAN12
2320995H1
1190
1337

18
LI:238576.2:2001JAN12
g1068687
1197
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18
LI:238576.2:2001JAN12
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1212
1333

18
LI:238576.2:2001JAN12
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1243
1337

18
LI:238576.2:2001JAN12
786346H1
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1326

18
LI:238576.2:2001JAN12
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1257
1333

18
LI:238576.2:2001JAN12
2278836H1
346
642

18
LI:238576.2:2001JAN12
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346
617

18
LI:238576.2:2001JAN12
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346
631

18
LI:238576.2:2001JAN12
6296712H1
348
729

18
LI:238576.2:2001JAN12
280390H1
349
730

18
LI:238576.2:2001JAN12
g1978517
352
741

18
LI:238576.2:2001JAN12
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355
567

18
LI:238576.2:2001JAN12
2208941H1
355
564

18
LI:238576.2:2001JAN12
5330792H1
360
621

18
LI:238576.2:2001JAN12
2504585H1
366
619

18
LI:238576.2:2001JAN12
g1812559
366
594

18
LI:238576.2:2001JAN12
g1383596
670
1071

18
LI:238576.2:2001JAN12
879714H1
672
936

18
LI:238576.2:2001JAN12
71302655V1
678
1271

18
LI:238576.2:2001JAN12
60123995B2
681
1276

18
LI:238576.2:2001JAN12
g3886420
692
839

18
LI:238576.2:2001JAN12
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691
867

18
LI:238576.2:2001JAN12
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692
1309

18
LI:238576.2:2001JAN12
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696
868

18
LI:238576.2:2001JAN12
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707
1347

18
LI:238576.2:2001JAN12
265346T6
711
1292

18
LI:238576.2:2001JAN12
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713
1348

18
LI:238576.2:2001JAN12
71219428V1
714
1338

18
LI:238576.2:2001JAN12
g2206609
715
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18
LI:238576.2:2001JAN12
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738
1367

18
LI:238576.2:2001JAN12
4938140H1
734
1041

18
LI:238576.2:2001JAN12
g2717345
755
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18
LI:238576.2:2001JAN12
71302491V1
758
1326

18
LI:238576.2:2001JAN12
134194F1
762
1333

18
LI:238576.2:2001JAN12
134194T6
767
1134

18
LI:238576.2:2001JAN12
71301214V1
773
1326

18
LI:238576.2:2001JAN12
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777
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18
LI:238576.2:2001JAN12
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786
1174

18
LI:238576.2:2001JAN12
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797
1349

18
LI:238576.2:2001JAN12
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797
980

18
LI:238576.2:2001JAN12
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388
995

18
LI:238576.2:2001JAN12
1379534H1
388
638

18
LI:238576.2:2001JAN12
2129696H1
403
675

18
LI:238576.2:2001JAN12
4938547H1
409
715

18
LI:238576.2:2001JAN12
2510749H1
415
770

18
LI:238576.2:2001JAN12
5659963H1
424
697

18
LI:238576.2:2001JAN12
1456371H1
421
678

18
LI:238576.2:2001JAN12
3604720H1
425
757

18
LI:238576.2:2001JAN12
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426
748

18
LI:238576.2:2001JAN12
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428
921

18
LI:238576.2:2001JAN12
2748683H1
429
693

18
LI:238576.2:2001JAN12
5659664H1
432
695

18
LI:238576.2:2001JAN12
71153764V1
435
949

18
LI:238576.2:2001JAN12
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453
784

18
LI:238576.2:2001JAN12
3257890H1
463
766

18
LI:238576.2:2001JAN12
2489834H1
464
705

18
LI:238576.2:2001JAN12
2244628H1
468
729

18
LI:238576.2:2001JAN12
1447415H1
470
748

18
LI:238576.2:2001JAN12
3769925H1
481
814

18
LI:238576.2:2001JAN12
6848683H1
481
1137

18
LI:238576.2:2001JAN12
851017H1
481
745

18
LI:238576.2:2001JAN12
3641003H1
486
718

18
LI:238576.2:2001JAN12
8262729LI1
488
1214

18
LI:238576.2:2001JAN12
591481H1
489
667

18
LI:238576.2:2001JAN12
591512H1
489
730

18
LI:238576.2:2001JAN12
2316586H1
489
744

18
LI:238576.2:2001JAN12
71153782V1
508
1061

18
LI:238576.2:2001JAN12
5274050H1
511
666

18
LI:238576.2:2001JAN12
608208H1
513
779

18
LI:238576.2:2001JAN12
5904564H1
513
843

18
LI:238576.2:2001JAN12
6061631H1
517
1142

18
LI:238576.2:2001JAN12
2866403H1
523
849

18
LI:238576.2:2001JAN12
g983400
526
895

18
LI:238576.2:2001JAN12
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543
799

18
LI:238576.2:2001JAN12
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551
861

18
LI:238576.2:2001JAN12
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559
809

18
LI:238576.2:2001JAN12
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587
874

18
LI:238576.2:2001JAN12
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590
858

18
LI:238576.2:2001JAN12
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592
1137

18
LI:238576.2:2001JAN12
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590
858

18
LI:238576.2:2001JAN12
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599
1090

18
LI:238576.2:2001JAN12
3246108H1
599
743

18
LI:238576.2:2001JAN12
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606
753

18
LI:238576.2:2001JAN12
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617
973

18
LI:238576.2:2001JAN12
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617
965

18
LI:238576.2:2001JAN12
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615
700

18
LI:238576.2:2001JAN12
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626
886

18
LI:238576.2:2001JAN12
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625
870

18
LI:238576.2:2001JAN12
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631
839

18
LI:238576.2:2001JAN12
71217985V1
632
819

18
LI:238576.2:2001JAN12
g2015041
637
1049

18
LI:238576.2:2001JAN12
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640
1218

18
LI:238576.2:2001JAN12
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647
1118

18
LI:238576.2:2001JAN12
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646
950

18
LI:238576.2:2001JAN12
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645
736

18
LI:238576.2:2001JAN12
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650
1275

18
LI:238576.2:2001JAN12
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651
1252

18
LI:238576.2:2001JAN12
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653
1014

18
LI:238576.2:2001JAN12
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660
1323

18
LI:238576.2:2001JAN12
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661
1344

18
LI:238576.2:2001JAN12
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662
961

18
LI:238576.2:2001JAN12
3501407H1
662
995

18
LI:238576.2:2001JAN12
g891119
668
951

18
LI:238576.2:2001JAN12
7062009H1
673
1090

18
LI:238576.2:2001JAN12
6401339H1
369
652

18
LI:238576.2:2001JAN12
3483783H1
373
645

18
LI:238576.2:2001JAN12
3375342H1
370
620

18
LI:238576.2:2001JAN12
5473124H1
376
544

18
LI:238576.2:2001JAN12
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375
647

18
LI:238576.2:2001JAN12
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375
621

18
LI:238576.2:2001JAN12
4302082H1
378
648

18
LI:238576.2:2001JAN12
516261R1
385
1026

18
LI:238576.2:2001JAN12
516261H1
385
622

18
LI:238576.2:2001JAN12
g2110639
799
1249

18
LI:238576.2:2001JAN12
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797
979

18
LI:238576.2:2001JAN12
1653928H1
809
1077

18
LI:238576.2:2001JAN12
71300941V1
814
1335

18
LI:238576.2:2001JAN12
70943453V1
814
979

18
LI:238576.2:2001JAN12
g2953761
815
1336

18
LI:238576.2:2001JAN12
g3933979
822
1336

18
LI:238576.2:2001JAN12
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820
1113

18
LI:238576.2:2001JAN12
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18
LI:238576.2:2001JAN12
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824
1333

18
LI:238576.2:2001JAN12
5559560H1
825
1111

18
LI:238576.2:2001JAN12
g4329635
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1333

19
LI:903914.3:2001JAN12
g6034066
2214
2619

19
LI:903914.3:2001JAN12
g3753899
2214
2626

19
LI:903914.3:2001JAN12
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6327
6446

19
LI:903914.3:2001JAN12
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5402
5595

19
LI:903914.3:2001JAN12
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5427
5675

19
LI:903914.3:2001JAN12
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5482
6060

19
LI:903914.3:2001JAN12
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5494
5819

19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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5607
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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5291
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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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7257
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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1875
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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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1875
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19
LI:903914.3:2001JAN12
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1875
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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1875
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19
LI:903914.3:2001JAN12
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2494

19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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1893
1960

19
LI:903914.3:2001JAN12
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1908
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19
LI:903914.3:2001JAN12
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1920
2572

19
LI:903914.3:2001JAN12
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1920
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
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LI:903914.3:2001JAN12
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1991
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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2037
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19
LI:903914.3:2001JAN12
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2042
2511

19
LI:903914.3:2001JAN12
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2046
2300

19
LI:903914.3:2001JAN12
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2047
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19
LI:903914.3:2001JAN12
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2582

19
LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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2581

19
LI:903914.3:2001JAN12
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2351

19
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2087
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19
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2087
2469

19
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2580

19
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2103
2590

19
LI:903914.3:2001JAN12
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2103
2438

19
LI:903914.3:2001JAN12
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19
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LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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2129
2619

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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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2138
2581

19
LI:903914.3:2001JAN12
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2140
2422

19
LI:903914.3:2001JAN12
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2619

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LI:903914.3:2001JAN12
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2145
2435

19
LI:903914.3:2001JAN12
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2619

19
LI:903914.3:2001JAN12
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2159
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LI:903914.3:2001JAN12
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2172
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19
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2625

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LI:903914.3:2001JAN12
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2620

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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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2624

19
LI:903914.3:2001JAN12
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2211
2421

19
LI:903914.3:2001JAN12
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1792
2420

19
LI:903914.3:2001JAN12
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1793
2051

19
LI:903914.3:2001JAN12
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1808
2043

19
LI:903914.3:2001JAN12
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1810
2234

19
LI:903914.3:2001JAN12
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1810
2087

19
LI:903914.3:2001JAN12
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2044

19
LI:903914.3:2001JAN12
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1818
1994

19
LI:903914.3:2001JAN12
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1821
2137

19
LI:903914.3:2001JAN12
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1828
2070

19
LI:903914.3:2001JAN12
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1829
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19
LI:903914.3:2001JAN12
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1830
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19
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1830
1991

19
LI:903914.3:2001JAN12
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1841
2048

19
LI:903914.3:2001JAN12
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1841
2318

19
LI:903914.3:2001JAN12
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1841
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19
LI:903914.3:2001JAN12
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1841
2137

19
LI:903914.3:2001JAN12
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1841
2122

19
LI:903914.3:2001JAN12
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1841
2172

19
LI:903914.3:2001JAN12
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1841
2077

19
LI:903914.3:2001JAN12
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1841
2056

19
LI:903914.3:2001JAN12
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1841
2037

19
LI:903914.3:2001JAN12
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1841
2038

19
LI:903914.3:2001JAN12
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1841
2034

19
LI:903914.3:2001JAN12
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1841
2006

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LI:903914.3:2001JAN12
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1841
2003

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LI:903914.3:2001JAN12
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1841
1949

19
LI:903914.3:2001JAN12
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1841
1989

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LI:903914.3:2001JAN12
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1841
1924

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LI:903914.3:2001JAN12
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1841
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LI:903914.3:2001JAN12
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1841
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19
LI:903914.3:2001JAN12
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1841
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LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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1851
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19
LI:903914.3:2001JAN12
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1856
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19
LI:903914.3:2001JAN12
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1866
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19
LI:903914.3:2001JAN12
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1869
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19
LI:903914.3:2001JAN12
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1875
2441

19
LI:903914.3:2001JAN12
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1871
2523

19
LI:903914.3:2001JAN12
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7419

19
LI:903914.3:2001JAN12
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6327
6462

19
LI:903914.3:2001JAN12
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4448
4692

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LI:903914.3:2001JAN12
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4451
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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6327
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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2213
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19
LI:903914.3:2001JAN12
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2215
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
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LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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6296
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19
LI:903914.3:2001JAN12
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6310
6553

19
LI:903914.3:2001JAN12
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6315
6566

19
LI:903914.3:2001JAN12
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6571

19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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5949
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19
LI:903914.3:2001JAN12
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6327
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19
LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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2249
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19
LI:903914.3:2001JAN12
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LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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2214
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19
LI:903914.3:2001JAN12
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1146
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19
LI:903914.3:2001JAN12
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1160
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19
LI:903914.3:2001JAN12
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1168
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19
LI:903914.3:2001JAN12
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1191
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19
LI:903914.3:2001JAN12
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1191
1573

19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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1202
1573

19
LI:903914.3:2001JAN12
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1219
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19
LI:903914.3:2001JAN12
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1242
1569

19
LI:903914.3:2001JAN12
3142223H1
1259
1540

19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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1303
1573

19
LI:903914.3:2001JAN12
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1305
1947

19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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1323
1951

19
LI:903914.3:2001JAN12
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1573

19
LI:903914.3:2001JAN12
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1377
1573

19
LI:903914.3:2001JAN12
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1385
1573

19
LI:903914.3:2001JAN12
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1388
1982

19
LI:903914.3:2001JAN12
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1427
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19
LI:903914.3:2001JAN12
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1437
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LI:903914.3:2001JAN12
5265270H2
1445
1573

19
LI:903914.3:2001JAN12
3720239H1
1482
1573

19
LI:903914.3:2001JAN12
116920R1
1486
1568

19
LI:903914.3:2001JAN12
116920H1
1486
1573

19
LI:903914.3:2001JAN12
7999947H1
1
479

19
LI:903914.3:2001JAN12
8004063H1
229
759

19
LI:903914.3:2001JAN12
g2191602
294
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19
LI:903914.3:2001JAN12
5540783H1
351
468

19
LI:903914.3:2001JAN12
359504H1
391
583

19
LI:903914.3:2001JAN12
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391
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19
LI:903914.3:2001JAN12
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503
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19
LI:903914.3:2001JAN12
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664
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19
LI:903914.3:2001JAN12
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839
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19
LI:903914.3:2001JAN12
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854
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19
LI:903914.3:2001JAN12
3492337F6
854
1124

19
LI:903914.3:2001JAN12
3492337H1
855
1122

19
LI:903914.3:2001JAN12
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952
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19
LI:903914.3:2001JAN12
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982
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19
LI:903914.3:2001JAN12
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1054
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19
LI:903914.3:2001JAN12
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1133
1593

19
LI:903914.3:2001JAN12
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1145
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19
LI:903914.3:2001JAN12
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1145
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LI:903914.3:2001JAN12
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6327
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19
LI:903914.3:2001JAN12
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19
LI:903914.3:2001JAN12
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7326
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19
LI:903914.3:2001JAN12
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7341
7423

19
LI:903914.3:2001JAN12
g2752668
7343
7419

19
LI:903914.3:2001JAN12
2130131H1
7363
7419

19
LI:903914.3:2001JAN12
7632580J1
3191
3294

19
LI:903914.3:2001JAN12
7464064H1
3567
4109

19
LI:903914.3:2001JAN12
7997457H1
584
1075

20
LI:150817.1:2001JAN12
490837H1
1
254

20
LI:150817.1:2001JAN12
490837R6
1
172

20
LI:150817.1:2001JAN12
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110
737

20
LI:150817.1:2001JAN12
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330
948

20
LI:150817.1:2001JAN12
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354
811

20
LI:150817.1:2001JAN12
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373
941

20
LI:150817.1:2001JAN12
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485
941

20
LI:150817.1:2001JAN12
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514
969

20
LI:150817.1:2001JAN12
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604
1148

20
LI:150817.1:2001JAN12
70660195V1
697
1306

20
LI:150817.1:2001JAN12
70658942V1
707
1217

20
LI:150817.1:2001JAN12
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718
1205

20
LI:150817.1:2001JAN12
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741
1315

20
LI:150817.1:2001JAN12
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775
1319

20
LI:150817.1:2001JAN12
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783
1322

20
LI:150817.1:2001JAN12
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786
1322

20
LI:150817.1:2001JAN12
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842
1334

20
LI:150817.1:2001JAN12
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860
1319

20
LI:150817.1:2001JAN12
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881
1322

20
LI:150817.1:2001JAN12
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931
1305

20
LI:150817.1:2001JAN12
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988
1322

20
LI:150817.1:2001JAN12
1943823T6
1013
1313

20
LI:150817.1:2001JAN12
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1025
1313

20
LI:150817.1:2001JAN12
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1115
1313

20
LI:150817.1:2001JAN12
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1208
1819

20
LI:150817.1:2001JAN12
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1236
1788

20
LI:150817.1:2001JAN12
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1241
1752

20
LI:150817.1:2001JAN12
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1631
1867

20
LI:150817.1:2001JAN12
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1643
1972

20
LI:150817.1:2001JAN12
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1642
2192

20
LI:150817.1:2001JAN12
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1643
1867

20
LI:150817.1:2001JAN12
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1646
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20
LI:150817.1:2001JAN12
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1646
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20
LI:150817.1:2001JAN12
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1646
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20
LI:150817.1:2001JAN12
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1741
2055

20
LI:150817.1:2001JAN12
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1817
2445

20
LI:150817.1:2001JAN12
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1925
2531

20
LI:150817.1:2001JAN12
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1982
2142

20
LI:150817.1:2001JAN12
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2088
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20
LI:150817.1:2001JAN12
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2092
2644

20
LI:150817.1:2001JAN12
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2124
2642

20
LI:150817.1:2001JAN12
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2156
2706

20
LI:150817.1:2001JAN12
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2211
2881

20
LI:150817.1:2001JAN12
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2216
2770

20
LI:150817.1:2001JAN12
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2216
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20
LI:150817.1:2001JAN12
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2227
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20
LI:150817.1:2001JAN12
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2330
2706

20
LI:150817.1:2001JAN12
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2471
3064

20
LI:150817.1:2001JAN12
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2496
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LI:150817.1:2001JAN12
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LI:150817.1:2001JAN12
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2529
3172

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LI:150817.1:2001JAN12
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2635
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LI:150817.1:2001JAN12
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2645
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LI:150817.1:2001JAN12
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2736
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LI:150817.1:2001JAN12
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2763
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LI:150817.1:2001JAN12
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LI:150817.1:2001JAN12
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3636
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LI:150817.1:2001JAN12
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LI:150817.1:2001JAN12
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3857
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LI:150817.1:2001JAN12
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3960
4415

21
LI:219627.1:2001JAN12
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21
LI:219627.1:2001JAN12
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1531
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21
LI:219627.1:2001JAN12
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1612
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LI:219627.1:2001JAN12
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21
LI:219627.1:2001JAN12
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2006
2158

21
LI:219627.1:2001JAN12
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21
LI:219627.1:2001JAN12
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1445
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LI:219627.1:2001JAN12
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905
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LI:219627.1:2001JAN12
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747
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21
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775
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21
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914
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21
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21
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21
LI:219627.1:2001JAN12
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905
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21
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531
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21
LI:219627.1:2001JAN12
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608
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21
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g2158893
600
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21
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803
1000

21
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383
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383
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1534

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1331
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1064
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LI:219627.1:2001JAN12
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977
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884
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21
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893
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LI:219627.1:2001JAN12
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847
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915
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LI:219627.1:2001JAN12
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802
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LI:219627.1:2001JAN12
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1516
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LI:219627.1:2001JAN12
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1191
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LI:219627.1:2001JAN12
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1316
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LI:219627.1:2001JAN12
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188
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21
LI:219627.1:2001JAN12
g6073244
1
438

22
LI:197812.4:2001JAN12
6845095F8
1
321

22
LI:197812.4:2001JAN12
6845095H1
1
338

22
LI:197812.4:2001JAN12
6845095T8
1
238

23
LI:101525.1:2001JAN12
71032233V1
1596
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23
LI:101525.1:2001JAN12
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1596
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LI:101525.1:2001JAN12
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1650
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LI:101525.1:2001JAN12
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2243

23
LI:101525.1:2001JAN12
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1754
2320

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LI:101525.1:2001JAN12
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2198

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LI:101525.1:2001JAN12
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1883
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LI:101525.1:2001JAN12
71291604V1
785
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LI:101525.1:2001JAN12
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LI:101525.1:2001JAN12
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883
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23
LI:101525.1:2001JAN12
70971439V1
902
1291

23
LI:101525.1:2001JAN12
70973738V1
955
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23
LI:101525.1:2001JAN12
g2268726
958
1221

23
LI:101525.1:2001JAN12
71292025V1
1038
1291

23
LI:101525.1:2001JAN12
71290752V1
1039
1293

23
LI:101525.1:2001JAN12
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1050
1291

23
LI:101525.1:2001JAN12
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1124
1258

23
LI:101525.1:2001JAN12
70973578V1
1155
1823

23
LI:101525.1:2001JAN12
71290943V1
1228
1687

23
LI:101525.1:2001JAN12
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2001

23
LI:101525.1:2001JAN12
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2216

23
LI:101525.1:2001JAN12
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23
LI:101525.1:2001JAN12
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23
LI:101525.1:2001JAN12
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23
LI:101525.1:2001JAN12
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23
LI:101525.1:2001JAN12
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1
470

23
LI:101525.1:2001JAN12
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147
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23
LI:101525.1:2001JAN12
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23
LI:101525.1:2001JAN12
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23
LI:101525.1:2001JAN12
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933

23
LI:101525.1:2001JAN12
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23
LI:101525.1:2001JAN12
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821

23
LI:101525.1:2001JAN12
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23
LI:101525.1:2001JAN12
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23
LI:101525.1:2001JAN12
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2057
2311

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LI:101525.1:2001JAN12
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2717

23
LI:101525.1:2001JAN12
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LI:101525.1:2001JAN12
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2311

24
LI:891123.1:2001JAN12
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177
619

24
LI:891123.1:2001JAN12
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24
LI:891123.1:2001JAN12
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24
LI:891123.1:2001JAN12
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1
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24
LI:891123.1:2001JAN12
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150
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25
LI:813500.1:2001JAN12
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2060

25
LI:813500.1:2001JAN12
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2074

25
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LI:813500.1:2001JAN12
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LI:813500.1:2001JAN12
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LI:813500.1:2001JAN12
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25
LI:813500.1:2001JAN12
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LI:813500.1:2001JAN12
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25
LI:813500.1:2001JAN12
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LI:813500.1:2001JAN12
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25
LI:813500.1:2001JAN12
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25
LI:813500.1:2001JAN12
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25
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LI:813500.1:2001JAN12
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25
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25
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25
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25
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25
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25
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25
LI:813500.1:2001JAN12
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25
LI:813500.1:2001JAN12
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25
LI:813500.1:2001JAN12
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LI:813500.1:2001JAN12
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LI:813500.1:2001JAN12
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LI:813500.1:2001JAN12
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LI:813500.1:2001JAN12
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25
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25
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25
LI:813500.1:2001JAN12
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25
LI:813500.1:2001JAN12
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25
LI:813500.1:2001JAN12
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25
LI:813500.1:2001JAN12
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25
LI:813500.1:2001JAN12
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25
LI:813500.1:2001JAN12
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25
LI:813500.1:2001JAN12
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931

25
LI:813500.1:2001JAN12
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1577
2053

25
LI:813500.1:2001JAN12
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25
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1577
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25
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25
LI:813500.1:2001JAN12
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25
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25
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25
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25
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2075

25
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25
LI:813500.1:2001JAN12
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2020

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25
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25
LI:813500.1:2001JAN12
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25
LI:813500.1:2001JAN12
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393
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25
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398
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25
LI:813500.1:2001JAN12
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1
372

25
LI:813500.1:2001JAN12
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100
600

25
LI:813500.1:2001JAN12
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1611
1978

25
LI:813500.1:2001JAN12
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1612
1826

25
LI:813500.1:2001JAN12
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963

25
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25
LI:813500.1:2001JAN12
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25
LI:813500.1:2001JAN12
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25
LI:813500.1:2001JAN12
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245
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25
LI:813500.1:2001JAN12
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259
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25
LI:813500.1:2001JAN12
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263
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25
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25
LI:813500.1:2001JAN12
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743

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25
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25
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25
LI:813500.1:2001JAN12
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2077

25
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25
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2003

25
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25
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430
1041

25
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539
931

26
LI:1037251.1:2001JAN12
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90
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243
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333
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1621

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1460

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1314

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1681

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1
419

26
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LI:2032187.1:2001JAN12
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293
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27
LI:2032187.1:2001JAN12
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922

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LI:2032187.1:2001JAN12
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LI:2032187.1:2001JAN12
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27
LI:2032187.1:2001JAN12
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27
LI:2032187.1:2001JAN12
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LI:2032187.1:2001JAN12
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LI:2032187.1:2001JAN12
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LI:2032187.1:2001JAN12
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27
LI:2032187.1:2001JAN12
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LI:347572.1:2001JAN12
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28
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2548

28
LI:347572.1:2001JAN12
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2748

28
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2672

28
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2571

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2059
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2347

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LI:222105.1:2001JAN12
5268184H1
2276
2433

33
LI:222105.1:2001JAN12
6982245H1
1868
2476

33
LI:222105.1:2001JAN12
g4123872
2693
2928

33
LI:222105.1:2001JAN12
3607719H1
1828
1928

33
LI:222105.1:2001JAN12
8097469H1
871
1443

33
LI:222105.1:2001JAN12
6753975H1
885
1499

33
LI:222105.1:2001JAN12
625468H1
792
1032

33
LI:222105.1:2001JAN12
6983060H1
853
1402

33
LI:222105.1:2001JAN12
8113670H1
855
1469

33
LI:222105.1:2001JANI2
1374191H1
2866
2928

33
LI:222105.1:2001JAN12
3998619H1
2649
2778

33
LI:222105.1:2001JAN12
397834T6
2655
2885

33
LI:222105.1:2001JAN12
g5543498
2660
2928

33
LI:222105.1:2001JAN12
2856775H1
2672
2928

33
LI:222105.1:2001JAN12
462594H1
2685
2873

33
LI:222105.1:2001JAN12
3740888H1
2687
2901

33
LI:222105.1:2001JAN12
3364340H1
2688
2931

33
LI:222105.1:2001JAN12
7699633H1
678
1162

33
LI:222105.1:2001JAN12
g5445748
2791
2928

33
LI:222105.1:2001JAN12
93230508
2860
2931

33
LI:222105.1:2001JAN12
5336032H1
2259
2477

33
LI:222105.1:2001JAN12
285132H1
1796
2005

33
LI:222105.1:2001JAN12
g4194131
2621
2931

33
LI:222105.1:2001JAN12
909685H1
2644
2928

33
LI:222105.1:2001JAN12
900923H1
2648
2913

33
LI:222105.1:2001JAN12
900922H1
2648
2890

33
LI:222105.1:2001JAN12
4302596H1
2649
2901

33
LI:222105.1:2001JAN12
3997210H1
2649
2804

33
LI:222105.1:2001JAN12
2648357H1
2597
2846

33
LI:222105.1:2001JAN12
1300340T6
2606
2889

33
LI:222105.1:2001JAN12
917086H1
1788
1971

33
LI:222105.1:2001JAN12
408689H1
1796
2058

33
LI:222105.1:2001JAN12
g2080434
2256
2716

33
LI:222105.1:2001JAN12
1842652R6
2247
2725

33
LI:222105.1:2001JAN12
1676867H1
2252
2463

33
LI:222105.1:2001JAN12
445738H1
2153
2430

33
LI:222105.1:2001JAN12
8193862H1
2165
2463

33
LI:222105.1:2001JAN12
2953417H1
2184
2483

33
LI:222105.1:2001JAN12
2925471H1
2208
2465

33
LI:222105.1:2001JAN12
715635H1
2174
2452

33
LI:222105.1:2001JAN12
717127H1
2174
2445

33
LI:222105.1:2001JAN12
1332387F6
2176
2522

33
LI:222105.1:2001JAN12
1402589H1
2176
2441

33
LI:222105.1:2001JAN12
818233H1
2211
2463

33
LI:222105.1:2001JAN12
6313074H1
2213
2463

33
LI:222105.1:2001JAN12
2443683H1
2227
2459

33
LI:222105.1:2001JAN12
1720394H1
2234
2457

33
LI:222105.1:2001JAN12
1842652H1
2247
2476

33
LI:222105.1:2001JAN12
3335135H1
567
739

33
LI:222105.1:2001JAN12
1756117H1
667
775

33
LI:222105.1:2001JAN12
2155703H1
672
875

33
LI:222105.1:2001JAN12
3239110H1
676
755

33
LI:222105.1:2001JAN12
g4665427
2740
2927

33
LI:222105.1:2001JAN12
g2036843
2741
2928

33
LI:222105.1:2001JAN12
1926455H1
2750
2928

33
LI:222105.1:2001JAN12
1926455R6
2750
2928

33
LI:222105.1:2001JAN12
1522791H1
2771
2928

33
LI:222105.1:2001JAN12
g1015246
2783
2916

33
LI:222105.1:2001JAN12
g1014231
2783
2928

33
LI:222105.1:2001JAN12
3149822H1
2787
2928

33
LI:222105.1:2001JAN12
3323427H1
562
831

33
LI:222105.1:2001JAN12
g3958413
2569
2677

33
LI:222105.1:2001JAN12
g2287807
2579
2928

33
LI:222105.1:2001JAN12
1300340F6
2579
2928

33
LI:222105.1:2001JAN12
1300340H1
2579
2831

33
LI:222105.1:2001JAN12
g2264076
2585
2928

33
LI:222105.1:2001JAN12
6504482H1
1751
1991

33
LI:222105.1:2001JAN12
341590H1
1756
2022

33
LI:222105.1:2001JAN12
378462H1
1756
1972

33
LI:222105.1:2001JAN12
1543868H1
1757
1969

33
LI:222105.1:2001JAN12
5924923H1
1788
2062

33
LI:222105.1:2001JAN12
2642319H1
505
710

33
LI:222105.1:2001JAN12
3771518H1
1732
2030

33
LI:222105.1:2001JAN12
2859109H1
1732
1935

33
LI:222105.1:2001JAN12
7354381H1
492
1084

33
LI:222105.1:2001JAN12
1926455T6
2739
2881

33
LI:222105.1:2001JAN12
5947131H1
2738
2931

33
LI:222105.1:2001JAN12
4072055H1
1710
1997

33
LI:222105.1:2001JAN12
8033408H1
1708
1855

33
LI:222105.1:2001JAN12
1211413R1
1710
2217

33
LI:222105.1:2001JAN12
1211413H1
1710
1975

33
LI:222105.1:2001JAN12
7762249J1
331
426

33
LI:222105.1:2001JAN12
7642129J1
470
783

33
LI:222105.1:2001JAN12
4306411H1
475
622

33
LI:222105.1:2001JAN12
7176225F8
320
438

33
LI:222105.1:2001JAN12
2571555H1
2714
2937

33
LI:222105.1:2001JAN12
g1955117
2716
2887

33
LI:222105.1:2001JAN12
g2432148
2731
2931

33
LI:222105.1:2001JAN12
4574566H1
2732
2929

33
LI:222105.1:2001JAN12
285455H1
2734
2928

33
LI:222105.1:2001JAN12
6854812H1
2714
2928

33
LI:222105.1:2001JAN12
4911394H1
2568
2835

33
LI:222105.1:2001JAN12
4500877H1
2570
2831

33
LI:222105.1:2001JAN12
g3959218
2558
2676

33
LI:222105.1:2001JAN12
2414524H1
2558
2665

33
LI:222105.1:2001JAN12
g2878154
2558
2722

33
LI:222105.1:2001JAN12
5305130H1
2041
2277

33
LI:222105.1:2001JAN12
1007852H1
2043
2342

33
LI:222105.1:2001JAN12
6529606H1
2048
2468

33
LI:222105.1:2001JAN12
5378309H1
2128
2389

33
LI:222105.1:2001JAN12
6350041H2
2050
2377

33
LI:222105.1:2001JAN12
6343875H1
2051
2322

33
LI:222105.1:2001JAN12
6350682H1
2051
2326

33
LI:222105.1:2001JAN12
3434235H1
2084
2327

33
LI:222105.1:2001JAN12
g3250400
2117
2298

33
LI:222105.1:2001JAN12
2430463H1
2117
2397

33
LI:222105.1:2001JAN12
512931H1
2153
2359

33
LI:222105.1:2001JAN12
g3421916
2127
2462

33
LI:222105.1:2001JAN12
7626196J1
2006
2477

33
LI:222105.1:2001JAN12
7701858H1
2006
2415

33
LI:222105.1:2001JAN12
7701858J2
2006
2123

33
LI:222105.1:2001JAN12
5550253H1
2022
2278

33
LI:222105.1:2001JAN12
916806H1
2026
2301

33
LI:222105.1:2001JAN12
2603907H1
1955
2212

33
LI:222105.1:2001JAN12
1386161H1
1974
2207

33
LI:222105.1:2001JAN12
1444911H1
1975
2241

33
LI:222105.1:2001JAN12
7120410H1
1685
1870

33
LI:222105.1:2001JAN12
7176225H1
320
441

33
LI:222105.1:2001JAN12
5921182H1
2707
2928

33
LI:222105.1:2001JAN12
983413T1
2707
2887

33
LI:222105.1:2001JAN12
2157952H1
2708
2933

33
LI:222105.1:2001JAN12
4069081H1
2708
2930

33
LI:222105.1:2001JAN12
810217H1
2710
2928

33
LI:222105.1:2001JAN12
900000H1
2711
2928

33
LI:222105.1:2001JAN12
900000T1
2711
2882

33
LI:222105.1:2001JAN12
900524H1
2711
2830

33
LI:222105.1:2001JAN12
2476377F6
1659
1949

33
LI:222105.1:2001JAN12
2476377H1
1659
1893

33
LI:222105.1:2001JAN12
7595853H1
1684
2120

33
LI:222105.1:2001JAN12
1789314H1
1650
1911

33
LI:222105.1:2001JAN12
476980H1
227
478

33
LI:222105.1:2001JAN12
7403149H1
256
438

33
LI:222105.1;2001JAN12
5198126H1
1893
2140

33
LI:222105.1:2001JAN12
4751130H1
1952
2240

33
LI:222105.1:2001JAN12
6803219J1
1387
1961

33
LI:222105.1:2001JAN12
6572119H1
1424
1728

33
LI:222105.1:2001JAN12
2918119H1
1426
1710

33
LI:222105.1:2001JAN12
2520896H1
1459
1703

33
LI:222105.1:2001JAN12
2187587H1
1483
1594

33
LI:222105.1:2001JAN12
2187433H1
1483
1599

33
LI:222105.1:2001JAN12
3280152W
1492
1755

33
LI:222105.1:2001JAN12
8109305W
1498
2140

33
LI:222105.1:2001JAN12
g3214187
1503
1859

33
LI:222105.1:2001JAN12
7740157H1
1502
2053

33
LI:222105.1:2001JAN12
g1970051
1503
1646

33
LI:222105.1:2001JAN12
3322816H1
1525
1801

33
LI:222105.1:2001JAN12
7283089H1
1557
2133

33
LI:222105.1:2001JAN12
1650438H1
1560
1740

33
LI:222105.1:2001JAN12
7386335H1
1
214

33
LI:222105.1:2001JAN12
8122932H1
59
383

33
LI:222105.1:2001JAN12
6356420F8
100
436

33
LI:222105.1:2001JAN12
2495754H1
115
348

33
LI:222105.1:2001JAN12
7469345H1
210
644

33
LI:222105.1:2001JAN12
7406641H1
1
353

33
LI:222105.1:2001JAN12
g2910345
1
57

33
LI:222105.1:2001JAN12
6753975J1
1
363

33
LI:222105.1:2001JAN12
g5848785
1
345

33
LI:222105.1:2001JAN12
g2080358
2557
2915

33
LI:222105.1:2001JAN12
6937583H1
2558
2756

33
LI:222105.1:2001JAN12
6803219H1
1887
2459

33
LI:222105.1:2001JAN12
3358989H1
1868
2098

33
LI:222105.1:2001JAN12
5134450H1
1870
2127

33
LI:222105.1:2001JAN12
2612419H1
1305
1582

33
LI:222105.1:2001JAN12
2112293H1
1359
1608

33
LI:222105.1:2001JAN12
2624024H1
2697
2928

33
LI:222105.1:2001JAN12
2548561H1
2697
2928

33
LI:222105.1:2001JAN12
3272683H1
2698
2928

33
LI:222105.1:2001JAN12
547730H1
2698
2928

33
LI:222105.1:2001JAN12
2888190H1
2701
2931

33
LI:222105.1:2001JAN12
1701864H1
2701
2897

33
LI:222105.1:2001JAN12
1417478H1
2705
2928

33
LI:222105.1:2001JAN12
983413H1
2707
2928

33
LI:222105.1:2001JAN12
056819H1
2695
2900

33
LI:222105.1:2001JAN12
2734088H1
2696
2929

33
LI:222105.1:2001JAN12
2761594H1
2697
2928

33
LI:222105.1:2001JAN12
7398940H1
1090
1641

33
LI:222105.1:2001JAN12
7398390H1
1092
1641

33
LI:222105.1:2001JAN12
7398401H1
1137
1641

33
LI:222105.1:2001JAN12
3597056H1
1177
1354

33
LI:222105.1:2001JAN12
7407244H1
1177
1410

33
LI:222105.1:2001JAN12
7699633J1
1202
1842

33
LI:222105.1:2001JAN12
6945777H1
1241
1603

33
LI:222105.1:2001JAN12
2763913H1
1242
1502

33
LI:222105.1:2001JAN12
7762249H1
1270
1693

33
LI:222105.1:2001JAN12
7703861H1
906
1433

33
LI:222105.1:2001JAN12
7397959H1
998
1641

33
LI:222105.1:2001JAN12
7100230H1
1026
1089

33
LI:222105.1:2001JAN12
g4176133
2548
2931

33
LI:222105.1:2001JAN12
g3230671
2548
2931

33
LI:222105.1:2001JAN12
g4874876
2548
2928

33
LI:222105.1:2001JAN12
g4453467
2548
2927

33
LI:222105.1:2001JAN12
g5671047
2548
2934

33
LI:222105.1:2001JAN12
g6085943
2548
2928

33
LI:222105.1:2001JAN12
g3002121
2548
2719

33
LI:222105.1:2001JAN12
805806H1
2548
2717

33
LI:222105.1:2001JAN12
g4188610
2548
2926

33
LI:222105.1:2001JAN12
777275R1
2554
2928

33
LI:222105.1:2001JAN12
777275H1
2554
2774

33
LI:222105.1:2001JAN12
7456830H1
2540
2753

33
LI:222105.1:2001JAN12
6272171H2
2540
2944

33
LI:222105.1:2001JAN12
5379306H1
2542
2702

33
LI:222105.1:2001JAN12
g4110835
2544
2928

33
LI:222105.1:2001JAN12
g4187376
2544
2931

33
LI:222105.1:2001JAN12
5375234H1
2546
2675

33
LI:222105.1:2001JAN12
g3693080
2547
2928

33
LI:222105.1:2001JAN12
079984H1
2547
2636

33
LI:222105.1:2001JAN12
g8364535
2548
2939

33
LI:222105.1:2001JAN12
2809175H1
2277
2470

33
LI:222105.1:2001JAN12
1957384H1
2280
2527

33
LI:222105.1:2001JAN12
916258H1
2286
2421

33
LI:222105.1:2001JAN12
1359150H1
2305
2463

33
LI:222105.1:2001JAN12
3838392H1
2366
2519

33
LI:222105.1:2001JAN12
2643055H1
2387
2476

33
LI:222105.1:2001JAN12
1842652T6
2468
2879

33
LI:222105.1:2001JAN12
4304712H1
2538
2814

33
LI:222105.1:2001JAN12
2292893H1
2694
2930

33
LI:222105.1:2001JAN12
2944459H1
2694
2913

34
LI:816737.2:2001JAN12
6396780H1
3207
3426

34
LI:816737.2:2001JAN12
2910364H1
3241
3498

34
LI:816737.2:2001JAN12
g1989191
1954
2341

34
LI:816737.2:2001JAN12
g4620385
2516
2700

34
LI:816737.2:2001JAN12
754388H1
3194
3450

34
LI:816737.2:2001JAN12
7041613H1
3199
3799

34
LI:816737.2:2001JAN12
6398585H1
3207
3488

34
LI:816737.2:2001JAN12
2105028H1
1951
2207

34
LI:816737.2:2001JAN12
g7151890
1926
2327

34
LI:816737.2:2001JAN12
g5526096
1921
2322

34
LI:816737.2:2001JAN12
6411534H1
1505
2054

34
LI:816737.2:2001JAN12
7618511H1
1513
2046

34
LI:816737.2:2001JAN12
4147335H1
1576
1891

34
LI:816737.2:2001JAN12
5540901H1
1633
1856

34
LI:816737.2:2001JAN12
2910019H1
1639
1928

34
LI:816737.2:2001JAN12
6410893H1
1645
1977

34
LI:816737.2:2001JAN12
8110880H1
1724
2324

34
LI:816737.2:2001JAN12
8024726J1
1774
2417

34
LI:816737.2:2001JAN12
7993975H1
1779
2348

34
LI:816737.2:2001JAN12
6592403H1
1799
2433

34
LI:816737.2:2001JAN12
7263053H1
1800
2347

34
LI:816737.2:2001JAN12
2911091H1
1803
2074

34
LI:816737.2:2001JAN12
2909285H1
1813
2093

34
LI:816737.2:2001JAN12
5730613H1
1887
2147

34
LI:816737.2:2001JAN12
g7236539
1897
2327

34
LI:816737.2:2001JAN12
g6199128
1899
2313

34
LI:816737.2:2001JAN12
g1897788
1168
1251

34
LI:816737.2:2001JAN12
2913215H1
3163
3431

34
LI:816737.2:2001JAN12
6411420H1
2506
3054

34
LI:816737.2:2001JAN12
7619120J1
2356
2964

34
LI:816737.2:2001JAN12
g7278272
2466
2704

34
LI:816737.2:2001JAN12
g4523480
2366
2782

34
LI:816737.2:2001JAN12
3925302H1
2474
2768

34
LI:816737.2:2001JAN12
g705891
2438
2744

34
LI:816737.2:2001JAN12
g7044021
2354
2702

34
LI:816737.2:2001JAN12
6408778H1
2321
2692

34
LI:816737.2:2001JAN12
6413215H1
2821
3304

34
LI:816737.2:2001JAN12
2864306H1
2852
3117

34
LI:816737.2:2001JAN12
2911451H1
2904
3108

34
LI:816737.2:2001JAN12
6408549H1
2908
3508

34
LI:816737.2:2001JAN12
6409975H1
2909
3394

34
LI:816737.2:2001JAN12
3483490H1
2927
3213

34
LI:816737.2:2001JAN12
6405529H1
2945
3294

34
LI:816737.2:2001JAN12
6412773F8
3040
3603

34
LI:816737.2:2001JAN12
6412373H1
3040
3583

34
LI:816737.2;2001JAN12
6410744H1
3048
3364

34
LI:816737.2:2001JAN12
6410835H1
3049
3373

34
LI:816737.2:2001JAN12
6405083H1
3082
3392

34
LI:816737.2:2001JAN12
6412125H1
3136
3359

34
LI:816737.2:2001JAN12
g7155152
2297
2700

34
LI:816737.2:2001JAN12
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LI:816737.2:2001JAN12
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34
LI:816737.2:2001JAN12
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34
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34
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893
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34
LI:816737.2:2001JAN12
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953
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34
LI:816737.2:2001JAN12
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34
LI:816737.2:2001JAN12
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34
LI:816737.2:2001JAN12
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34
LI:816737.2:2001JAN12
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34
LI:816737.2:2001JAN12
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34
LI:816737.2:2001JAN12
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34
LI:816737.2:2001JAN12
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34
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34
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34
LI:816737.2:2001JAN12
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34
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34
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34
LI:816737.2:2001JAN12
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34
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34
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34
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34
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34
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34
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34
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34
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34
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34
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34
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34
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34
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34
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34
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LI:475524.1:2001JAN12
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37
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37
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37
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37
LI:814346.1:2001JAN12
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37
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37
LI:814346.1:2001JAN12
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37
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LI:814346.1:2001JAN12
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37
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37
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37
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37
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37
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37
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37
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37
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37
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37
LI:814346.1:2001JAN12
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37
LI:814346.1:2001JAN12
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37
LI:814346.1:2001JAN12
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37
LI:814346.1:2001JAN12
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37
LI:814346.1:2001JAN12
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37
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37
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38
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38
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38
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38
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38
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38
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38
LI:898195.6:2001JAN12
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38
LI:898195.6:2001JAN12
2318591R6
4059
4262

38
LI:898195.6:2001JAN12
5725624H1
3287
3901

38
LI:898195.6:2001JAN12
2538423H1
3277
3464

38
LI:898195.6:2001JAN12
71493831V1
2379
3004

38
LI:898195.6:2001JAN12
71489870V1
2371
3127

38
LI:898195.6:2001JAN12
7075767H1
1784
2335

38
LI:898195.6:2001JAN12
3814857H1
3277
3530

38
LI:898195.6:2001JAN12
g1319137
2725
3256

38
LI:898195.6:2001JAN12
909186H1
2668
2896

38
LI:898195.6:2001JAN12
499524319
2695
3153

38
LI:898195.6:2001JAN12
71493631V1
2685
3250

38
LI:898195.6:2001JAN12
71490430V1
1379
2115

38
LI:898195.6:2001JAN12
2269233H1
4039
4238

38
LI:898195.6:2001JAN12
2278423H1
4048
4318

38
LI:898195.6:2001JAN12
850139T6
4015
4335

38
LI:898195.6:2001JAN12
4204612H1
3268
3570

38
LI:898195.6:2001JAN12
4972615H1
3263
3555

38
LI:898195.6:2001JAN12
7748961H1
3181
3735

38
LI:898195.6:2001JAN12
g1201165
3251
3510

38
LI:898195.6:2001JAN12
4972491H1
3264
3554

38
LI:898195.6:2001JAN12
850139R6
3146
3372

38
LI:898195.6:2001JAN12
71490015V1
1375
1994

38
LI:898195.6:2001JAN12
70539842V1
1361
2008

38
LI:898195.6:2001JAN12
g2878100
3994
4405

38
LI:898195.6:2001JAN12
2268212H1
3139
3408

38
LI:898195.6:2001JAN12
2268285H1
3139
3399

38
LI:898195.6:2001JAN12
850139H1
3146
3332

38
LI:898195.6:2001JAN12
g823068
2671
3004

38
LI:898195.6:2001JAN12
398353916
2668
3226

38
LI:898195.6:2001JAN12
1495736H1
2668
2917

38
LI:898195.6:2001JAN12
71492961V1
2088
2733

38
LI:898195.6:2001JAN12
2268285R6
3139
3577

38
LI:898195.6:2001JAN12
71489542V1
1762
2347

38
LI:898195.6:2001JAN12
71489909V1
1345
1980

38
LI:898195.6:2001JAN12
71489910V1
1350
1947

38
LI:898195.6:2001JAN12
3622989H1
3958
4251

38
LI:898195.6:2001JAN12
g3430146
3972
4381

38
LI:898195.6:2001JAN12
g2115030
3993
4380

38
LI:898195.6:2001JAN12
g6472938
2655
2996

38
LI:898195.6:2001JAN12
g2229530
3950
4262

38
LI:898195.6:2001JAN12
4043165H1
3077
3243

38
LI:898195.6:2001JAN12
6286950H2
3100
3667

38
LI:898195.6:2001JAN12
218893H1
3130
3365

38
LI:898195.6:2001JAN12
2616038H1
3016
3242

38
LI:898195.6:2001JAN12
4570890H1
3052
3250

38
LI:898195.6:2001JAN12
71490796V1
2087
2750

38
LI:898195.6:2001JAN12
g1148373
3918
4238

38
LI:898195.6:2001JAN12
g5541266
3932
4256

38
LI:898195.6:2001JAN12
g5663591
3895
4377

38
LI:898195.6:2001JAN12
g4264588
2964
3250

38
LI:898195.6:2001JAN12
7033996H1
3007
3598

38
LI:898195.6:2001JAN12
1711980H1
2963
3194

38
LI:898195.6:2001JAN12
6918253H1
2655
3175

38
LI:898195.6:2001JAN12
g6474994
3891
4378

38
LI:898195.6:2001JAN12
71493906V1
2644
3250

38
LI:898195.6:2001JAN12
g6047753
2628
2996

38
LI:898195.6:2001JAN12
2447382F6
2628
3092

38
LI:898195.6:2001JAN12
2447382H1
2628
2864

38
LI:898195.6:2001JAN12
71491219V1
1642
2338

38
LI:898195.6:2001JAN12
4356674H1
1676
1815

38
LI:898195.6:2001JAN12
71514685V1
1736
2137

38
LI:898195.6:2001JAN12
71495018V1
1746
2480

38
LI:898195.6:2001JAN12
71493340V1
1753
2482

38
LI:898195.6:2001JAN12
110706R6
1751
2381

38
LI:898195.6:2001JAN12
6860682H1
1758
2285

38
LI:898195.6:2001JAN12
60208534U1
1756
2264

38
LI:898195.6:2001JAN12
60210281U2
1756
2264

38
LI:898195.6:2001JAN12
7447963T2
3863
4275

38
LI:898195.6:2001JAN12
1711980F6
2963
3503

38
LI:898195.6:2001JAN12
728574T6
2611
3203

38
LI:898195.6:2001JAN12
71491947V1
1332
2077

38
LI:898195.6:2001JAN12
g4329755
2947
3354

38
LI:898195.6:2001JAN12
g4308505
2594
3005

38
LI:898195.6:2001JAN12
3386565H1
2604
2769

38
LI:898195.6:2001JAN12
6466260H1
2611
3141

38
LI:898195.6:2001JAN12
6702126H1
1536
1671

38
LI:898195.6:2001JAN12
7055263H1
1569
2181

38
LI:898195.6:2001JAN12
71492674V1
1586
2247

38
LI:898195.6:2001JAN12
71491332V1
1600
2318

38
LI:898195.6:2001JAN12
71494832V1
1605
2259

38
LI:898195.6:2001JAN12
71495440V1
1550
2100

38
LI:898195.6:2001JAN12
2571272H1
2591
2851

38
LI:898195.6:2001JAN12
g3920068
2590
2996

38
LI:898195.6:2001JAN12
71490723V1
2082
2749

38
LI:898195.6:2001JAN12
71490472V1
1331
1961

38
LI:898195.6:2001JAN12
71492182V1
1336
1894

38
LI:898195.6:2001JAN12
71494843V1
1348
1999

38
LI:898195.6:2001JAN12
6610413T2
2868
3183

38
LI:898195.6:2001JAN12
71493130V1
2095
2840

38
LI:898195.6:2001JAN12
71489915V1
1506
1950

38
LI:898195.6:2001JAN12
71494638V1
1317
2139

38
LI:898195.6:2001JAN12
71491632V1
1254
2040

38
LI:898195.6:2001JAN12
7196285H1
1259
1756

38
LI:898195.6:2001JAN12
71490973V1
1272
1981

38
LI:898195.6:2001JAN12
71494231V1
1283
1922

38
LI:898195.6:2001JAN12
70533396V1
1309
1708

38
LI:898195.6:2001JAN12
71493328V1
1332
2125

38
LI:898195.6:2001JAN12
6533967H1
2589
2888

38
LI:898195.6:2001JAN12
7159246H1
621
1181

38
LI:898195.6:2001JAN12
5617155R6
628
829

38
LI:898195.6:2001JAN12
5547413H1
631
718

38
LI:898195.6:2001JAN12
71492138V1
631
1174

38
LI:898195.6:2001JAN12
g766423
643
934

38
LI:898195.6:2001JAN12
4995243H1
653
914

38
LI:898195.6:2001JAN12
4995243F9
671
1280

38
LI:898195.6:2001JAN12
71503002V1
700
887

38
LI:898195.6:2001JAN12
2408642H1
737
958

38
LI:898195.6:2001JAN12
71493077V1
811
1434

38
LI:898195.6:2001JAN12
7444781T2
819
1344

38
LI:898195.6:2001JAN12
71490327V1
938
1428

38
LI:898195.6:2001JAN12
6973635H1
959
1574

38
LI:898195.6:2001JAN12
7037377H1
980
1596

38
LI:898195.6:2001JAN12
71494208V1
1041
1789

38
LI:898195.6:2001JAN12
71495382V1
1067
1692

38
LI:898195.6:2001JAN12
71490356V1
1086
1861

38
LI:898195.6:2001JAN12
5369675H1
1092
1339

38
LI:898195.6:2001JAN12
71491107V1
1111
1917

38
LI:898195.6:2001JAN12
g2207950
1155
1682

38
LI:898195.6:2001JAN12
71504614V1
1214
1929

38
LI:898195.6:2001JAN12
7591984H1
1196
1844

38
LI:898195.6:2001JAN12
71504314V1
1249
1930

38
LI:898195.6:2001JAN12
71489617V1
1227
2008

38
LI:898195.6:2001JAN12
71492957V1
1240
2042

38
LI:898195.6:2001JAN12
71507314V1
1248
1930

38
LI:898195.6:2001JAN12
g1948998
597
886

38
LI:898195.6:2001JAN12
6619702H1
598
1202

38
LI:898195.6:2001JAN12
5617155R8
625
829

38
LI:898195.6:2001JAN12
2749245H1
3849
4126

38
LI:898195.6:2001JAN12
4511284H1
3851
4141

38
LI:898195.6:2001JAN12
2268285T6
3824
4217

38
LI:898195.6:2001JAN12
6933855H1
2108
2711

38
LI:898195.6:2001JAN12
71493386V1
2077
2473

38
LI:898195.6:2001JAN12
2671118F6
591
1165

38
LI:898195.6:2001JAN12
3629862H1
591
882

38
LI:898195.6:2001JAN12
2671118H1
591
850

38
LI:898195.6:2001JAN12
71490246V1
2815
3378

38
LI:898195.6:2001JAN12
2298219H1
2815
3073

38
LI:898195.6:2001JAN12
3593805
2523
3001

38
LI:898195.6:2001JAN12
2207851
2554
2995

38
LI:898195.6:2001JAN12
g3593268
2571
3003

38
LI:898195.6:2001JAN12
71491946V1
2077
2828

38
LI:898195.6:2001JAN12
g2007104
578
942

38
LI:898195.6:2001JAN12
g4650843
578
2996

38
LI:898195.6:2001JAN12
7255387H1
561
1147

38
LI:898195.6:2001JAN12
g7022682
562
2996

38
LI:898195.6:2001JAN12
1987775H1
563
762

38
LI:898195.6:2001JAN12
8125276H1
522
1147

38
LI:898195.6:2001JAN12
7997854H1
525
1114

38
LI:898195.6:2001JAN12
4179939H1
539
774

38
LI:898195.6:2001JAN12
8003770H1
541
1146

38
LI:898195.6:2001JAN12
7994210H1
503
1088

38
LI:898195.6:2001JAN12
7267059H2
502
1062

38
LI:898195.6:2001JAN12
8116748H1
512
1121

38
LI:898195.6:2001JAN12
8133184H1
511
1160

38
LI:898195.6:2001JAN12
6349561H2
518
868

38
LI:898195.6:2001JAN12
71491559V1
473
868

38
LI:898195.6:2001JAN12
3983539F6
474
856

38
LI:898195.6:2001JAN12
3983539H1
474
691

38
LI:898195.6:2001JAN12
71513785V1
474
672

38
LI:898195.6:2001JAN12
71493903V1
474
1000

38
LI:898195.6:2001JAN12
71495030V1
474
988

38
LI:898195.6:2001JAN12
5649669H1
3713
3947

38
LI:898195.6:2001JAN12
7451851T1
3750
4266

38
LI:898195.6:2001JAN12
g5394901
3758
4241

38
LI:898195.6:2001JAN12
2405018H1
3784
4019

38
LI:898195.6:2001JAN12
g7038644
2800
3250

38
LI:898195.6:2001JAN12
2088126H1
2516
2778

38
LI:898195.6:2001JAN12
71489807V1
2053
2766

38
LI:898195.6:2001JAN12
71491508V1
1536
2373

38
LI:898195.6:2001JAN12
3786850H1
3692
3931

38
LI:898195.6:2001JAN12
3116845H1
2788
3096

38
LI:898195.6:2001JAN12
4760765H1
2790
3108

38
LI:898195.6:2001JAN12
3112816T6
2774
3210

38
LI:898195.6:2001JAN12
71491496V1
2043
2815

38
LI:898195.6:2001JAN12
5544139H1
1467
1627

38
LI:898195.6:2001JAN12
6531363H1
1513
1891

38
LI:898195.6:2001JAN12
71494444V1
1500
2116

38
LI:898195.6:2001JAN12
71493302V1
474
1120

38
LI:898195.6:2001JAN12
6377935H1
2765
3054

38
LI:898195.6:2001JAN12
70538653V1
1993
2494

38
LI:898195.6:2001JAN12
71494757V1
1992
2782

38
LI:898195.6:2001JAN12
7162193H1
2011
2614

38
LI:898195.6:2001JAN12
g1993262
2012
2449

38
LI:898195.6:2001JAN12
71489883V1
2016
2645

38
LI:898195.6:2001JAN12
71493184V1
2045
2673

38
LI:898195.6:2001JAN12
71492658V1
1984
2624

38
LI:898195.6:2001JAN12
71492344V1
1465
2115

38
LI:898195.6:2001JAN12
71492153V1
474
1114

38
LI:898195.6:2001JAN12
g2216813
3690
4096

38
LI:898195.6:2001JAN12
3886194H1
3659
3913

38
LI:898195.6:2001JAN12
1403832W
3675
3945

38
LI:898195.6:2001JAN12
71494313V1
1938
2701

38
LI:898195.6:2001JAN12
6584035H1
43
630

38
LI:898195.6:2001JAN12
5645518H1
464
740

38
LI:898195.6:2001JAN12
g5112262
2765
3250

38
LI:898195.6:2001JAN12
60208536U1
2513
2996

38
LI:898195.6:2001JAN12
71495479V1
2462
2994

38
LI:898195.6:2001JAN12
7041488H1
2493
3093

38
LI:898195.6:2001JAN12
g5755441
2509
3000

38
LI:898195.6:2001JAN12
995180H1
1844
2101

38
LI:898195.6:2001JAN12
71493412V1
1854
2504

38
LI:898195.6:2001JAN12
7637472H1
1862
2350

38
LI:898195.6:2001JAN12
2303263H1
1879
2159

38
LI:898195.6:2001JAN12
71492496V1
1886
2391

38
LI:898195.6:2001JAN12
71492871V1
1900
2680

38
LI:898195.6:2001JAN12
71490023V1
1899
2582

38
LI:898195.6:2001JAN12
71495435V1
1901
2608

38
LI:898195.6:2001JAN12
71492029V1
1912
2709

38
LI:898195.6:2001JAN12
71503961V1
1926
2352

38
LI:898195.6:2001JAN12
71491939V1
1914
2710

38
LI:898195.6:2001JAN12
6355207H1
1920
2250

38
LI:898195.6:2001JAN12
995015R1
1844
2118

38
LI:898195.6:2001JAN12
995188H1
1844
2100

38
LI:898195.6:2001JAN12
71492712V1
1833
2509

38
LI:898195.6:2001JAN12
6610413H2
1876
2444

38
LI:898195.6:2001JAN12
3625291H1
3659
3930

38
LI:898195.6:2001JAN12
7445377T1
3589
4132

38
LI:898195.6:2001JAN12
g4438704
2758
2997

38
LI:898195.6:2001JAN12
3723637H1
2447
2739

38
LI:898195.6:2001JAN12
71518506V1
2460
2666

38
LI:898195.6:2001JAN12
6587005H1
2348
2896

38
LI:898195.6:2001JAN12
728574H1
2326
2567

38
LI:898195.6:2001JAN12
728574R6
2325
2737

38
LI:898195.6:2001JAN12
71492930V1
1428
2014

38
LI:898195.6:2001JAN12
71491594V1
1428
2015

38
LI:898195.6:2001JAN12
71495469V1
1448
2116

38
LI:898195.6:2001JAN12
71518483V1
1447
1809

38
LI:898195.6:2001JAN12
5046976H1
1
267

38
LI:898195.6:2001JAN12
7367170H1
9
408

38
LI:898195.6:2001JAN12
523396H1
3333
3578

38
LI:898195.6:2001JAN12
g2229528
3342
3748

38
LI:898195.6:2001JAN12
2679381H1
3345
3671

38
LI:898195.6:2001JAN12
g2115320
3377
3784

38
LI:898195.6:2001JAN12
2279854H1
3464
3736

38
LI:898195.6:2001JAN12
772531H1
3475
3755

38
LI:898195.6:2001JAN12
4826651H1
3506
3764

38
LI:898195.6:2001JAN12
1784781H1
3517
3736

38
LI:898195.6:2001JAN12
4721426H1
3526
3802

38
LI:898195.6:2001JAN12
5167963H1
3529
3618

38
LI:898195.6:2001JAN12
2754913H1
3542
3807

38
LI:898195.6:2001JAN12
7027158H1
2751
3250

38
LI:898195.6:2001JAN12
g795429
2757
2996

38
LI:898195.6:2001JAN12
2447382T6
2723
3250

38
LI:898195.6:2001JAN12
4712875H1
2720
2981

38
LI:898195.6:2001JAN12
743887T6
2725
3204

38
LI:898195.6:2001JAN12
5600615H1
2721
2996

38
LI:898195.6:2001JAN12
2671118T6
2443
2956

38
LI:898195.6:2001JAN12
71505439V1
2406
2842

38
LI:898195.6:2001JAN12
2909248H1
2408
2617

38
LI:898195.6:2001JAN12
4656934H1
2422
2646

38
LI:898195.6:2001JAN12
3110269F6
2145
2493

38
LI:898195.6:2001JAN12
3110269H1
2146
2458

38
LI:898195.6:2001JAN12
g1319256
2145
2736

38
LI:898195.6:2001JAN12
g827697
2195
2495

38
LI:898195.6:2001JAN12
71492270V1
2221
2983

38
LI:898195.6:2001JAN12
71495453V1
2253
2933

38
LI:898195.6:2001JAN12
3251857H1
2254
2598

38
LI:898195.6:2001JAN12
71492005V1
2255
2840

38
LI:898195.6:2001JAN12
71493164V1
2259
2695

38
LI:898195.6:2001JAN12
71489641V1
2284
2994

38
LI:898195.6:2001JAN12
71491634V1
2305
2677

38
LI:898195.6:2001JAN12
71492036V1
2307
3081

38
LI:898195.6:2001JAN12
4976428H1
2317
2587

38
LI:898195.6:2001JAN12
71495122V1
2324
2574

38
LI:898195.6:2001JAN12
71490407V1
2331
3065

38
LI:898195.6:2001JAN12
71493706V1
2089
2628

38
LI:898195.6:2001JAN12
71492686V1
2135
2893

38
LI:898195.6:2001JAN12
71493381V1
2141
2840

38
LI:898195.6:2001JAN12
71493965V1
1406
2052

38
LI:898195.6:2001JAN12
71494883V1
1423
2052

38
LI:898195.6:2001JAN12
2722154F6
4154
4253

38
LI:898195.6:2001JAN12
g2881456
4176
4384

38
LI:898195.6:2001JAN12
g2216716
4207
4379

39
LI:210497.2:2001JAN12
4741947F8
1
417

39
LI:210497.2:2001JAN12
4741947H1
1
279

40
LI:110297.4:2001JAN12
70786692V1
1157
1753

40
LI:110297.4:2001JAN12
2856676H1
951
1243

40
LI:110297.4:2001JAN12
70648923V1
961
1555

40
LI:110297.4:2001JAN12
70783945V1
565
995

40
LI:110297.4:2001JAN12
70781901V1
565
1024

40
LI:110297.4:2001JAN12
4671416H1
1868
2110

40
LI:110297.4:2001JAN12
2913921H1
1898
2157

40
LI:110297.4:2001JAN12
g1164230
1545
1861

40
LI:110297.4:2001JAN12
2689635H1
1577
1823

40
LI:110297.4:2001JAN12
4116764H1
1391
1517

40
LI:110297.4:2001JAN12
70023942D1
1311
1860

40
LI:110297.4:2001JAN12
70029139D1
1311
1843

40
LI:110297.4:2001JAN12
5600036H1
1319
1841

40
LI:110297.4:2001JAN12
70782999V1
1186
1706

40
LI:110297.4:2001JAN12
70783823V1
1265
1863

40
LI:110297.4:2001JAN12
g1165659
1285
1555

40
LI:110297.4:2001JAN12
g2206862
1302
1801

40
LI:110297.4:2001JAN12
70783080V1
948
1503

40
LI:110297.4:2001JAN12
2104414H1
1566
1853

40
LI:110297.4:2001JAN12
4520010H1
323
570

40
LI:110297.4:2001JAN12
3983764F6
82
369

40
LI:110297.4:2001JAN12
3983764H1
82
384

40
LI:110297.4:2001JAN12
7995279H1
162
721

40
LI:110297.4:2001JAN12
3029528H1
193
458

40
LI:110297.4:2001JAN12
70784202V1
565
1192

40
LI:110297.4:2001JAN12
724533R7
565
1108

40
LI:110297.4:2001JAN12
70785603V1
565
1066

40
LI:110297.4:2001JAN12
70785643V1
565
1033

40
LI:110297.4:2001JAN12
70026552D1
1588
2072

40
LI:110297.4:2001JAN12
3742365H1
1593
1846

40
LI:110297.4:2001JAN12
1462519H1
1612
1858

40
LI:110297.4:2001JAN12
7726316J1
1022
1687

40
LI:110297.4:2001JAN12
70782675V1
1053
1702

40
LI:110297.4:2001JAN12
g1925661
1133
1519

40
LI:110297.4:2001JAN12
70025407D1
1907
2215

40
LI:110297.4:2001JAN12
70029342D1
1907
2215

40
LI:110297.4:2001JAN12
70029258D1
1907
2214

40
LI:110297.4:2001JAN12
g2206464
1913
2086

40
LI:110297.4:2001JAN12
g3674744
1920
2086

40
LI:110297.4:2001JAN12
724533T7
1941
2429

40
LI:110297.4:2001JAN12
70781763V1
948
1589

40
LI:110297.4:2001JAN12
3449854H1
951
1207

40
LI:110297.4:2001JAN12
3449854R6
951
1538

40
LI:110297.4:2001JAN12
2856676F6
951
1442

40
LI:110297.4:2001JAN12
70027082D1
951
1395

40
LI:110297.4:2001JAN12
70783970V1
1153
1790

40
LI:110297.4:2001JAN12
3449854T6
1941
2422

40
LI:110297.4:2001JAN12
70783020V1
967
1571

40
LI:110297.4:2001JAN12
5753034H1
699
1210

40
LI:110297.4:2001JAN12
70782038V1
565
1079

40
LI:110297.4:2001JAN12
70783480V1
566
1037

40
LI:110297.4:2001JAN12
g1920167
1133
1585

40
LI:110297.4:2001JAN12
3449608H1
1138
1335

40
LI:110297.4:2001JAN12
70785513V1
903
1460

40
LI:110297.4:2001JAN12
70785412V1
1402
1960

40
LI:110297.4:2001JAN12
70026769D1
1394
1799

40
LI:110297.4:2001JAN12
70025601D1
1410
1846

40
LI:110297.4:2001JAN12
70781899V1
1401
2051

40
LI:110297.4:2001JAN12
70028622D1
1435
1846

40
LI:110297.4:2001JAN12
6309439H1
1472
1996

40
LI:110297.4:2001JAN12
6515321H1
1482
1795

40
LI:110297.4:2001JAN12
70786740V1
898
1508

40
LI:110297.4:2001JAN12
70787200V1
1868
2415

40
LI:110297.4:2001JAN12
353306R6
1579
2002

40
LI:110297.4:2001JAN12
353306H1
1579
1810

40
LI:110297.4:2001JAN12
70785718V1
1580
1846

40
LI:110297.4:2001JAN12
70028710D1
1587
1846

40
LI:110297.4:2001JAN12
70784006V1
1348
1919

40
LI:110297.4:2001JAN12
70782667V1
1342
1845

40
LI:110297.4:2001JAN12
70786499V1
1357
1846

40
LI:110297.4:2001JAN12
2263980H1
1546
1789

40
LI:110297.4:2001JAN12
70782057V1
1849
2407

40
LI:110297.4:2001JAN12
7726316H1
660
1219

40
LI:110297.4:2001JAN12
1624704H1
460
681

40
LI:110297.4:2001JAN12
g2001257
536
835

40
LI:110297.4:2001JAN12
70786774V1
556
1184

40
LI:110297.4:2001JAN12
70786966V1
556
1186

40
LI:110297.4:2001JAN12
353306T6
1954
2410

40
LI:110297.4:2001JAN12
70027255D1
1979
2215

40
LI:110297.4:2001JAN12
70029345D1
1988
2215

40
LI:110297.4:2001JAN12
1353179F1
1995
2471

40
LI:110297.4:2001JAN12
1353179H1
1995
2245

40
LI:110297.4:2001JAN12
3149528H1
2009
2284

40
LI:110297.4:2001JAN12
3983764T6
2058
2442

40
LI:110297.4:2001JAN12
608911H1
2062
2309

40
LI:110297.4:2001JAN12
2256872H1
2078
2332

40
LI:110297.4:2001JAN12
g1142341
2088
2465

40
LI:110297.4:2001JAN12
g3336427
2090
2472

40
LI:110297.4:2001JAN12
3782340H1
2091
2358

40
LI:110297.4:2001JAN12
g3835146
2102
2474

40
LI:110297.4:2001JAN12
g3742491
2102
2465

40
LI:110297.4:2001JAN12
g3835091
2102
2474

40
LI:110297.4:2001JAN12
g3927350
2110
2465

40
LI:110297.4:2001JAN12
g7039435
2143
2465

40
LI:110297.4:2001JAN12
g1148144
2169
2470

40
LI:110297.4:2001JAN12
3738323H1
2184
2470

40
LI:110297.4:2001JAN12
2856676T6
2185
2422

40
LI:110297.4:2001JAN12
904425H1
2215
2467

40
LI:110297.4:2001JAN12
g1925662
2226
2476

40
LI:110297.4:2001JAN12
3451908T6
2243
2413

40
LI:110297.4:2001JAN12
g5639182
2254
2467

40
LI:110297.4:2001JAN12
2375691T6
2266
2427

40
LI:110297.4:2001JAN12
5874106H1
2267
2470

40
LI:110297.4:2001JAN12
2375691F6
2273
2468

40
LI:110297.4:2001JAN12
2375691H1
2273
2464

40
LI:110297.4:2001JAN12
g1920007
2346
2476

40
LI:110297.4:2001JAN12
724533H1
565
797

40
LI:110297.4:2001JAN12
70785147V1
565
1236

40
LI:110297.4:2001JAN12
g4089290
1
392

40
LI:110297.4:2001JAN12
4028996H1
1621
1846

40
LI:110297.4:2001JAN12
70025095D1
1623
2033

40
LI:110297.4:2001JAN12
70786818V1
566
1210

40
LI:110297.4:2001JAN12
70781846V1
585
1233

40
LI:110297.4:2001JAN12
2960369H2
636
943

40
LI:110297.4:2001JAN12
1987506H1
643
856

40
LI:110297.4:2001JAN12
70786215V1
973
1420

40
LI:110297.4:2001JAN12
2840594H1
1730
1951

40
LI:110297.4:2001JAN12
70026254D1
1774
2215

40
LI:110297.4:2001JAN12
70785140V1
1868
2465

40
LI:110297.4:2001JAN12
70027257D1
1868
2215

41
LI:2051312.1:2001JAN12
5496076H1
1
239

41
LI:2051312.1:2001JAN12
71633936V1
321
781

41
LI:2051312.1:2001JAN12
71635207V1
340
781

41
LI:2051312.1:2001JAN12
71634519V1
291
781

41
LI:2051312.1:2001JAN12
71634870V1
369
781

41
LI:2051312.1:2001JAN12
71635242V1
423
780

41
LI:2051312.1:2001JAN12
71607340V1
621
781

41
LI:2051312.1:2001JAN12
71637573V1
124
781

41
LI:2051312.1:2001JAN12
71637992V1
147
781

41
LI:2051312.1:2001JAN12
71639182V1
96
780

41
LI:2051312.1:2001JAN12
71638290V1
362
780

41
LI:2051312.1:2001JAN12
71636821V1
309
779

41
LI:2051312.1:2001JAN12
5496076R6
328
779

41
LI:2051312.1:2001JAN12
71635391V1
381
779

41
LI:2051312.1:2001JAN12
71638124V1
155
692

41
LI:2051312.1:2001JAN12
71637632V1
66
781

41
LI:2051312.1:2001JAN12
71638247V1
86
781

41
LI:2051312.1:2001JAN12
71638024V1
59
781

41
LI:2051312.1:2001JAN12
71635765V1
85
781

41
LI:2051312.1:2001JAN12
71638514V1
97
781

41
LI:2051312.1:2001JAN12
71634090V1
91
781

41
LI:2051312.1:2001JAN12
71634725V1
73
781

41
LI:2051312.1:2001JAN12
71635487V1
113
781

41
LI:2051312.1:2001JAN12
2586589H1
395
663

41
LI:2051312.1:2001JAN12
71638551V1
163
780

41
LI:2051312.1:2001JAN12
71635931V1
213
781

41
LI:2051312.1:2001JAN12
71637959V1
316
780

41
LI:2051312.1:2001JAN12
71638163V1
328
782

41
LI:2051312.1:2001JAN12
71635455V1
344
781

41
LI:2051312.1:2001JAN12
6045011F8
624
1213

41
LI:2051312.1:2001JAN12
6045011H1
619
1201

41
LI:2051312.1:2001JAN12
6560080H1
489
1084

41
LI:2051312.1:2001JAN12
6850955H1
518
1045

41
LI:2051312.1:2001JAN12
6560080F8
489
997

41
LI:2051312.1:2001JAN12
71633951V1
45
778

41
LI:2051312.1:2001JAN12
3566902F6
115
792

41
LI:2051312.1:2001JAN12
71638659V1
146
781

41
LI:2051312.1:2001JAN12
71634906V1
35
781

41
LI:2051312.1:2001JAN12
5496076F6
1
441

41
LI:2051312.1:2001JAN12
4074128H1
127
425

41
LI:2051312.1:2001JAN12
3568923H1
98
406

41
LI:2051312.1:2001JAN12
3566902H1
114
352

41
LI:2051312.1:2001JAN12
7203805H1
1071
1637

41
LI:2051312.1:2001JAN12
5092837H1
1501
1636

41
LI:2051312.1:2001JAN12
6560080T8
1089
1364

41
LI:2051312.1:2001JAN12
270703817
740
1324

41
LI:2051312.1:2001JAN12
3566902T6
657
1297

41
LI:2051312.1:2001JAN12
6045011J1
726
1290

41
LI:2051312.1:2001JAN12
6045011R8
803
1290

41
LI:2051312.1:2001JAN12
2815381H1
57
116

42
LI:350272.2:2001JAN12
174100216
1041
1512

42
LI:350272.2:2001JAN12
3844367H1
626
942

42
LI:350272.2:2001JAN12
960820T6
1037
1515

42
LI:350272.2:2001JAN12
1741002R6
1041
1550

42
LI:350272.2:2001JAN12
4010536H1
1031
1266

42
LI:350272.2:2001JAN12
644238R6
834
1410

42
LI:350272.2:2001JAN12
644238H1
834
892

42
LI:350272.2:2001JAN12
2511182H1
1024
1352

42
LI:350272.2:2001JAN12
7764948H1
133
494

42
LI:350272.2:2001JAN12
g2270187
1175
1553

42
LI:350272.2:2001JAN12
6383176H1
1297
1512

42
LI:350272.2:2001JAN12
g4618967
1154
1550

42
LI:350272.2:2001JAN12
g2575091
620
875

42
LI:350272.2:2001JAN12
2206242H1
619
871

42
LI:350272.2:2001JAN12
4241989H1
408
742

42
LI:350272.2:2001JAN12
g2674996
415
827

42
LI:350272.2:2001JAN12
g1186534
421
828

42
LI:350272.2:2001JAN12
7326176H1
442
909

42
LI:350272.2:2001JAN12
6311958H1
458
892

42
LI:350272.2:2001JAN12
6201854H1
470
912

42
LI:350272.2:2001JAN12
3559406H1
469
574

42
LI:350272.2:2001JAN12
5306551H1
1287
1419

42
LI:350272.2:2001JAN12
5306583H1
1288
1449

42
LI:350272.2:2001JAN12
7082642H1
1
232

42
LI:350272.2:2001JAN12
6758676J1
1
582

42
LI:350272.2:2001JAN12
8176753H1
117
790

42
LI:350272.2:2001JAN12
g2669493
1153
1552

42
LI:350272.2:2001JAN12
2116744H1
810
892

42
LI:350272.2:2001JAN12
1864387H1
804
892

42
LI:350272.2:2001JAN12
g5755616
1126
1556

42
LI:350272.2:2001JAN12
g2465965
1143
1556

42
LI:350272.2:2001JAN12
3740987H1
323
625

42
LI:350272.2:2001JAN12
5020588T1
338
779

42
LI:350272.2:2001JAN12
603382H1
320
576

42
LI:350272.2:2001JAN12
2538770H1
320
536

42
LI:350272.2:2001JAN12
5020696T1
319
780

42
LI:350272.2:2001JAN12
g4074869
1113
1556

42
LI:350272.2:2001JAN12
6606673H1
1076
1551

42
LI:350272.2:2001JAN12
g4970896
1077
1555

42
LI:350272.2:2001JAN12
g4125734
1079
1539

42
LI:350272.2:2001JAN12
g3741618
1094
1559

42
LI:350272.2:2001JAN12
g6038705
1110
1550

42
LI:350272.2:2001JAN12
2697244H1
565
854

42
LI:350272.2:2001JAN12
4665428H1
570
845

42
LI:350272.2:2001JAN12
708387H1
587
865

42
LI:350272.2:2001JAN12
g3213833
597
826

42
LI:350272.2:2001JAN12
2715220H1
603
850

42
LI:350272.2:2001JAN12
6486886H1
617
1161

42
LI:350272.2:2001JAN12
g2577306
1301
1550

42
LI:350272.2:2001JAN12
644238T6
1287
1516

42
LI:350272.2:2001JAN12
6326064H1
1288
1553

42
LI:350272.2:2001JAN12
6552652H1
762
1293

42
LI:350272.2:2001JAN12
4138187H1
785
892

42
LI:350272.2:2001JAN12
6552052H1
762
1227

42
LI:350272.2:2001JAN12
g5812197
1335
1536

42
LI:350272.2:2001JAN12
1684883H1
1344
1550

42
LI:350272.2:2001JAN12
3932451H1
1363
1550

42
LI:350272.2:2001JAN12
211293H1
1365
1557

42
LI:350272.2:2001JAN12
211696H1
1365
1550

42
LI:350272.2:2001JAN12
633648H1
1372
1563

42
LI:350272.2:2001JAN12
3565543H1
1384
1508

42
LI:350272.2:2001JAN12
g2359505
1463
1550

42
LI:350272.2:2001JAN12
g4649884
1466
1544

42
LI:350272.2:2001JAN12
6615126H1
1488
1550

42
LI:350272.2:2001JAN12
7322258H1
232
865

42
LI:350272.2:2001JAN12
2127622H1
260
527

42
LI:350272.2:2001JAN12
1684883T6
1061
1515

42
LI:350272.2:2001JAN12
1684883F6
1061
1550

42
LI:350272.2:2001JAN12
3621890H1
1050
1132

42
LI:350272.2:2001JAN12
211114H1
1051
1101

42
LI:350272.2:2001JAN12
581813T6
1052
1512

42
LI:350272.2:2001JAN12
g2820887
1053
1553

42
LI:350272.2:2001JAN12
5766360H1
665
1183

42
LI:350272.2:2001JAN12
3016843H1
692
892

42
LI:350272.2:2001JAN12
g5755074
1271
1556

42
LI:350272.2:2001JAN12
6843381H1
1271
1382

42
LI:350272.2:2001JAN12
g2669985
1217
1446

42
LI:350272.2:2001JAN12
2561156H1
1226
1522

42
LI:350272.2:2001JAN12
g5364704
1229
1551

42
LI:350272.2:2001JAN12
1637245H1
1207
1419

42
LI:350272.2:2001JAN12
g4267877
1205
1544

42
LI:350272.2:2001JAN12
g4267523
1203
1544

42
LI:350272.2:2001JAN12
g4267458
1203
1544

42
LI:350272.2:2001JAN12
g2900340
636
815

42
LI:350272.2:2001JAN12
2805489H1
659
914

42
LI:350272.2:2001JAN12
581813R6
193
553

42
LI:350272.2:2001JAN12
g3307326
1184
1559

42
LI:350272.2:2001JAN12
g2715505
1185
1556

42
LI:350272.2:2001JAN12
4353485H1
1050
1139

42
LI:350272.2:2001JAN12
g4079566
1300
1550

42
LI:350272.2:2001JAN12
1888879H1
510
800

42
LI:350272.2:2001JAN12
6058322H1
555
894

42
LI:350272.2:2001JAN12
4121623H1
558
857

42
LI:350272.2:2001JAN12
960820R6
562
938

42
LI:350272.2:2001JAN12
960820H1
562
841

42
LI:350272.2:2001JAN12
3490063H1
471
771

42
LI:350272.2:2001JAN12
g7153657
480
827

42
LI:350272.2:2001JAN12
8167852H1
492
1120

42
LI:350272.2:2001JAN12
5865088H1
182
475

42
LI:350272.2:2001JAN12
581813H1
193
465

42
LI:350272.2:2001JAN12
g5397025
1182
1550

42
LI:350272.2:2001JAN12
g855861
1192
1547

42
LI:350272.2:2001JAN12
4010319H1
1041
1260

42
LI:350272.2:2001JAN12
1741002H1
1041
1125

42
LI:350272.2:2001JAN12
2650967H1
1042
1224

42
LI:350272.2:2001JAN12
4013519H1
1050
1264

42
LI:350272.2:2001JAN12
4353493H1
1050
1141

43
LI:1085472.4:2001JAN12
7987779H1
2601
3017

43
LI:1085472.4:2001JAN12
3781866F7
2601
3002

43
LI:1085472.4:2001JAN12
71367354V1
2601
3099

43
LI:1085472.4:2001JAN12
71366182V1
2601
3145

43
LI:1085472.4:2001JAN12
3869194F6
2601
2942

43
LI:1085472.4:2001JAN12
3781866F6
2601
2804

43
LI:1085472.4:2001JAN12
71370688V1
2601
2727

43
LI:1085472.4:2001JAN12
3869194H1
2601
2725

43
LI:1085472.4:2001JAN12
1802440H1
2601
2701

43
LI:1085472.4:2001JAN12
658162H1
2601
2686

43
LI:1085472.4:2001JAN12
70016474D1
2601
2657

43
LI:1085472.4:2001JAN12
70015482D1
2601
2657

43
LI:1085472.4:2001JAN12
4108457H1
2954
3221

43
LI:1085472.4:2001JAN12
7340664H1
2972
3597

43
LI:1085472.4:2001JAN12
4933091H1
2992
3230

43
LI:1085472.4:2001JAN12
70016523D1
3003
3496

43
LI:1085472.4:2001JAN12
4341990H1
3016
3265

43
LI:1085472.4:2001JAN12
5407487H1
3043
3296

43
LI:1085472.4:2001JAN12
2617950H1
3055
3318

43
LI:1085472.4:2001JAN12
6603445H1
3067
3206

43
LI:1085472.4:2001JAN12
4650576H1
3068
3354

43
LI:1085472.4:2001JAN12
6395196H1
3071
3225

43
LI:1085472.4:2001JAN12
70017457D1
3096
3489

43
LI:1085472.4:2001JAN12
70014308D1
2468
2882

43
LI:1085472.4:2001JAN12
g1472629
2597
2923

43
LI:1085472.4:2001JAN12
71372045V1
2601
2727

43
LI:1085472.4:2001JAN12
3386621H1
2845
3004

43
LI:1085472.4:2001JAN12
7630053J1
2857
3498

43
LI:1085472.4:2001JAN12
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2863
3095

43
LI:1085472.4:2001JAN12
1823282H1
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43
LI:1085472.4:2001JAN12
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43
LI:1085472.4:2001JAN12
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2885
3278

43
LI:1085472.4:2001JAN12
5511808H1
2907
3155

43
LI:1085472.4:2001JAN12
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2933
3510

43
LI:1085472.4:2001JAN12
3781871H1
2601
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43
LI:1085472.4:2001JAN12
3781867H1
2601
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43
LI:1085472.4:2001JAN12
1802440F6
2601
2792

43
LI:1085472.4:2001JAN12
4327538H1
2601
2686

43
LI:1085472.4:2001JAN12
2763622H1
2624
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43
LI:1085472.4:2001JAN12
4202242H1
2627
2780

43
LI:1085472.4:2001JAN12
7426017H1
2630
3252

43
LI:1085472.4:2001JAN12
6599647H1
2651
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43
LI:1085472.4:2001JAN12
7766094J1
2657
3061

43
LI:1085472.4:2001JAN12
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2670
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43
LI:1085472.4:2001JAN12
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2670
3177

43
LI:1085472.4:2001JAN12
6937773R8
2679
3358

43
LI:1085472.4:2001JAN12
4820435H1
2701
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43
LI;1085472.4:2001JAN12
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2772
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43
LI:1085472.4:2001JAN12
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2773
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43
LI:1085472.4:2001JAN12
2509043F6
2824
3248

43
LI:1085472.4:2001JAN12
2509043H1
2824
3085

43
LI:1085472.4:2001JAN12
2778212F6
2827
3334

43
LI:1085472.4:2001JAN12
2778212H1
2827
3081

43
LI:1085472.4:2001JAN12
2872122H1
2830
3134

43
LI:1085472.4:2001JAN12
6298454H1
2601
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43
LI:1085472.4:2001JAN12
4934841F6
1207
1762

43
LI:1085472.4:2001JAN12
7383285H1
1261
1609

43
LI:1085472.4:2001JAN12
3082109H1
1310
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43
LI:1085472.4:2001JAN12
649924H1
1328
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43
LI:1085472.4:2001JAN12
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2037

43
LI:1085472.4:2001JAN12
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1489
1998

43
LI:1085472.4:2001JAN12
5032294H1
1590
1762

43
LI:1085472.4:2001JAN12
7667194H1
1600
2184

43
LI:1085472.4:2001JAN12
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1740
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43
LI:1085472.4:2001JAN12
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43
LI:1085472.4:2001JAN12
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43
LI:1085472.4:2001JAN12
7762086J1
1823
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43
LI:1085472.4:2001JAN12
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1833
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43
LI:1085472.4:2001JAN12
3040429H1
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2132

43
LI:1085472.4:2001JAN12
7979208H1
1950
2304

43
LI:1085472.4:2001JAN12
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1976
2304

43
LI:1085472.4:2001JAN12
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1999
2304

43
LI:1085472.4:2001JAN12
8099682H1
2137
2750

43
LI:1085472.4:2001JAN12
6937773H1
2145
2304

43
LI:1085472.4:2001JAN12
6937773F8
2146
2744

43
LI:1085472.4:2001JAN12
1729838H1
2228
2304

43
LI:1085472.4:2001JAN12
8053354J1
452
1017

43
LI:1085472.4:2001JAN12
7384254H1
466
1017

43
LI:1085472.4:2001JAN12
8267087H1
500
875

43
LI:1085472.4:2001JAN12
6355031F8
805
1230

43
LI:1085472.4:2001JAN12
6993231H1
864
1255

43
LI:1085472.4:2001JAN12
7765508J1
918
1556

43
LI:1085472.4:2001JAN12
2765041H1
1004
1175

43
LI:1085472.4:2001JAN12
6355463H1
1009
1238

43
LI:1085472.4:2001JAN12
6355432H1
1028
1238

43
LI:1085472.4:2001JAN12
8013915H1
1064
1584

43
LI:1085472.4:2001JAN12
6488391F9
1068
1687

43
LI:1085472.4:2001JAN12
6488391H1
1068
1474

43
LI:1085472.4:2001JAN12
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1144
1286

43
LI:1085472.4:2001JAN12
4031565F8
1148
1661

43
LI:1085472.4:2001JAN12
4934841H1
1207
1491

43
LI:1085472.4:2001JAN12
7766520J1
1
555

43
LI:1085472.4:2001JAN12
7385651H1
68
706

43
LI:1085472.4:2001JAN12
g6656244
180
616

43
LI:1085472.4:2001JAN12
7766520H1
205
885

43
LI:1085472.4:2001JAN12
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326
647

43
LI:1085472.4:2001JAN12
7728326H1
434
867

43
LI:1085472.4:2001JAN12
g2107297
1
390

44
LI:1190272.1:2001JAN12
5722642H1
70
626

44
LI:1190272.1:2001JAN12
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738
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44
LI:1190272.1:2001JAN12
g1792770
751
1082

44
LI:1190272.1:2001JAN12
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765
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44
LI:1190272.1:2001JAN12
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772
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44
LI:1190272.1:2001JAN12
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647
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44
LI:1190272.1:2001JAN12
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720
1083

44
LI:1190272.1:2001JAN12
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725
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44
LI:1190272.1:2001JAN12
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296

44
LI:1190272.1:2001JAN12
6335579H1
53
639

44
LI:1190272.1:2001JAN12
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53
336

44
LI:1190272.1:2001JAN12
6294680H1
52
296

44
LI:1190272.1:2001JAN12
7719486J1
1
379

44
LI:1190272.1:2001JAN12
g6650542
1
1087

44
LI:1190272.1:2001JAN12
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131
649

44
LI:1190272.1:2001JAN12
002242H1
645
1055

44
LI:1190272.1:2001JAN12
7742643H1
484
957

44
LI:1190272.1:2001JAN12
g1162646
638
1080

44
LI:1190272.1:2001JAN12
g3598316
579
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44
LI:1190272.1:2001JAN12
g3432529
599
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44
LI:1190272.1:2001JAN12
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604
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44
LI:1190272.1:2001JAN12
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611
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44
LI:1190272.1:2001JAN12
g3231777
614
1089

44
LI:1190272.1:2001JAN12
g2197997
854
1080

44
LI:1190272.1:2001JAN12
6589156H1
523
1089

44
LI:1190272.1:2001JAN12
92052982
920
1090

44
LI:1190272.1:2001JAN12
g3801217
775
1083

44
LI:1190272.1:2001JAN12
70513918V1
75
602

44
LI:1190272.1:2001JAN12
5970131H1
70
614

44
LI:1190272.1:2001JAN12
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217
600

44
LI:1190272.1:2001JAN12
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330
1030

44
LI:1190272.1:2001JAN12
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330
621

44
LI:1190272.1:2001JAN12
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593

44
LI:1190272.1:2001JAN12
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633

44
LI:1190272.1:2001JAN12
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598

44
LI:1190272.1:2001JAN12
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591

44
LI:1190272.1:2001JAN12
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589

44
LI:1190272.1:2001JAN12
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330
583

44
LI:1190272.1:2001JAN12
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330
581

44
LI:1190272.1:2001JAN12
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131
649

44
LI:1190272.1:2001JAN12
5603809H1
186
444

44
LI:1190272.1:2001JAN12
70433375D2
217
600

44
LI:1190272.1:2001JAN12
g2167301
615
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44
LI:1190272.1:2001JAN12
91765314
618
1087

44
LI:1190272.1:2001JAN12
5468034H1
70
280

44
LI:1190272.1:2001JAN12
g1162429
704
1080

44
LI:1190272.1:2001JAN12
g4113765
732
1073

44
LI:1190272.1:2001JAN12
5350781H1
82
337

44
LI:1190272.1:2001JAN12
6717604F8
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626

44
LI:1190272.1:2001JAN12
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626

44
LI:1190272.1:2001JAN12
6335465H1
85
645

44
LI:1190272.1:2001JAN12
4923429F8
85
532

44
LI:1190272.1:2001JAN12
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57
658

44
LI:1190272.1:2001JAN12
5973544H1
90
617

44
LI:1190272.1:2001JAN12
91331187
111
573

44
LI:1190272.1:2001JAN12
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123
597

44
LI:1190272.1:2001JAN12
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130
531

44
LI:1190272.1:2001JAN12
7612525J1
1
416

44
LI:1190272.1:2001JAN12
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60
484

44
LI:1190272.1:2001JAN12
6717604H1
73
445

44
LI:1190272.1:2001JAN12
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75
636

44
LI:1190272.1:2001JAN12
70514963V1
75
633

44
LI:1190272.1:2001JAN12
6963747H1
434
887

44
LI:1190272.1:2001JAN12
6717604T8
477
912

44
LI:1190272.1:2001JAN12
6959682H1
330
651

44
LI:1190272.1:2001JAN12
6282416H1
330
416

44
LI:1190272.1:2001JAN12
5724550T8
415
733

44
LI:1190272.1:2001JAN12
001418H1
550
999

44
LI:1190272.1:2001JAN12
g5848464
579
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44
LI:1190272.1:2001JAN12
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64
141

45
LI:1086797.1:2001JAN12
7204577R8
203
633

45
LI:1086797.1:2001JAN12
1445162H1
3136
3409

45
LI:1086797.1:2001JAN12
4754255H1
3180
3424

45
LI:1086797.1:2001JAN12
7006595H1
3240
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45
LI:1086797.1:2001JAN12
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3245
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45
LI:1086797.1:2001JAN12
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3246
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45
LI:1086797.1:2001JAN12
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45
LI:1086797.1:2001JAN12
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45
LI:1086797.1:2001JAN12
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3257

45
LI:1086797.1:2001JAN12
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3098
3180

45
LI:1086797.1:2001JAN12
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3516

45
LI:1086797.1:2001JAN12
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3098
3508

45
LI:1086797.1:2001JAN12
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3098
3359

45
LI:1086797.1:2001JAN12
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2724
3000

45
LI:1086797.1:2001JAN12
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2837
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45
LI:1086797.1:2001JAN12
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45
LI:1086797.1:2001JAN12
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3582

45
LI:1086797.1:2001JAN12
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3000
3054

45
LI:1086797.1:2001JAN12
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3098
3521

45
LI:1086797.1:2001JAN12
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3521

45
LI:1086797.1:2001JAN12
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45
LI:1086797.1:2001JAN12
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914
1427

45
LI:1086797.1:2001JAN12
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912
1329

45
LI:1086797.1:2001JAN12
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1672

45
LI:1086797.1:2001JAN12
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145
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45
LI:1086797.1:2001JAN12
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2317
2829

45
LI:1086797.1:2001JAN12
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45
LI:1086797.1:2001JAN12
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3009

45
LI:1086797.1:2001JAN12
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3041

45
LI:1086797.1:2001JAN12
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45
LI:1086797.1:2001JAN12
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45
LI:1086797.1:2001JAN12
3282052H1
2537
2800

45
LI:1086797.1:2001JAN12
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45
LI:1086797.1:2001JAN12
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3198

45
LI:1086797.1:2001JAN12
2889461F6
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45
LI:1086797.1:2001JAN12
2889461H1
2701
2876

45
LI:1086797.1:2001JAN12
6824374H1
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45
LI:1086797.1:2001JAN12
7199082F8
776
1278

45
LI:1086797.1:2001JAN12
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45
LI:1086797.1:2001JAN12
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45
LI:1086797.1:2001JAN12
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2817

45
LI:1086797.1:2001JAN12
3605176T9
2299
2807

45
LI:1086797.1:2001JAN12
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1677

45
LI:1086797.1:2001JAN12
7165980R8
678
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45
LI:1086797.1:2001JAN12
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483
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45
LI:1086797.1:2001JAN12
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45
LI:1086797.1:2001JAN12
7197662F8
547
1242

45
LI:1086797.1:2001JAN12
7165980R6
650
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45
LI:1086797.1:2001JAN12
6935088R6
290
872

45
LI:1086797.1:2001JAN12
3605176F8
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45
LI:1086797.1:2001JAN12
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45
LI:1086797.1:2001JAN12
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1657
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45
LI:1086797.1:2001JAN12
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45
LI:1086797.1:2001JAN12
4153824H1
1673
1906

45
LI:1086797.1:2001JAN12
3766035H1
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2058

45
LI:1086797.1:2001JAN12
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2320

45
LI:1086797.1:2001JAN12
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1606

45
LI:1086797.1:2001JAN12
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45
LI:1086797.1:2001JAN12
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45
LI:1086797.1:2001JAN12
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1129
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45
LI:1086797.1:2001JAN12
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45
LI:1086797.1:2001JAN12
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45
LI:1086797.1:2001JAN12
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1078
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45
LI:1086797.1:2001JAN12
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45
LI:1086797.1:2001JAN12
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45
LI:1086797.1:2001JAN12
7163357F8
1031
1703

45
LI:1086797.1:2001JAN12
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1
301

45
LI:1086797.1:2001JAN12
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1
405

45
LI:1086797.1:2001JAN12
6935088H1
1
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45
LI:1086797.1:2001JAN12
g766318
3246
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46
LI:1144466.1:2001JAN12
5872651H1
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1610

46
LI:1144466.1:2001JAN12
570945T6
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2114

46
LI:1144466.1:2001JAN12
6417564H1
2046
2148

46
LI:1144466.1:2001JAN12
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549
995

46
LI:1144466.1:2001JAN12
570945H1
549
837

46
LI:1144466.1:2001JAN12
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534
1247

46
LI:1144466.1:2001JAN12
70936971V1
535
1194

46
LI:1144466.1:2001JAN12
70947577V1
539
1181

46
LI:1144466.1:2001JAN12
5487221H1
593
856

46
LI:1144466.1:2001JAN12
70947867V1
599
1121

46
LI:1144466.1:2001JAN12
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LI:1144466.1:2001JAN12
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46
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46
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46
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46
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LI:1144466.1:2001JAN12
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46
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46
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46
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46
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46
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46
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46
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46
LI:1144466.1:2001JAN12
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46
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47
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47
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47
LI:1147914.1:2001JAN12
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47
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48
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48
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48
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48
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48
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48
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48
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48
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48
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LI:758086.1:2001JAN12
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1154
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48
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48
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48
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LI:758086.1:2001JAN12
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333
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48
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LI:758086.1:2001JAN12
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48
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48
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LI:765245.5:2001JAN12
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49
LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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49
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49
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LI:765245.5:2001JAN12
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1101
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49
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LI:765245.5:2001JAN12
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49
LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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49
LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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88
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LI:765245.5:2001JAN12
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49
LI:765245.5:2001JAN12
8039196J1
170
923

49
LI:765245.5:2001JAN12
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194
737

49
LI:765245.5:2001JAN12
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246
895

49
LI:765245.5:2001JAN12
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933

49
LI:765245.5:2001JAN12
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986

49
LI:765245.5:2001JAN12
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933

49
LI:765245.5:2001JAN12
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49
LI:765245.5:2001JAN12
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1744

49
LI:765245.5:2001JAN12
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49
LI:765245.5:2001JAN12
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49
LI:765245.5:2001JAN12
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49
LI:765245.5:2001JAN12
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923
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49
LI:765245.5:2001JAN12
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49
LI:765245.5:2001JAN12
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49
LI:765245.5:2001JAN12
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49
LI:765245.5:2001JAN12
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49
LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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49
LI:765245.5:2001JAN12
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49
LI:765245.5:2001JAN12
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49
LI:765245.5:2001JAN12
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49
LI:765245.5:2001JAN12
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49
LI:765245.5:2001JAN12
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49
LI:765245.5:2001JAN12
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668
929

49
LI:765245.5:2001JAN12
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49
LI:765245.5:2001JAN12
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755
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49
LI:765245.5:2001JAN12
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49
LI:765245.5:2001JAN12
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49
LI:765245.5:2001JAN12
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49
LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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49
LI:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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L1:765245.5:2001JAN12
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LI:765245.5:2001JAN12
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50
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LI:335608.2:2001JAN12
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50
LI:335608.2:2001JAN12
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50
LI:335608.2:2001JAN12
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50
LI:335608.2:2001JAN12
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LI:335608.2:2001JAN12
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LI:335608.2:2001JAN12
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LI:335608.2:2001JAN12
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LI:335608.2:2001JAN12
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LI:335608.2:2001JAN12
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LI:335608.2:2001JAN12
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50
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LI:405795.1:2001JAN12
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LI:405795.1:2001JAN12
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LI:405795.1:2001JAN12
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LI:405795.1:2001JAN12
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LI:405795.1:2001JAN12
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LI:405795.1:2001JAN12
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LI:405795.1:2001JAN12
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LI:405795.1:2001JAN12
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LI:405795.1:2001JAN12
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LI:405795.1:2001JAN12
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LI:405795.1:2001JAN12
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52
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53
LI:239245.3:2001JAN12
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53
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53
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LI:239245.3:2001JAN12
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53
LI:239245.3:2001JAN12
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53
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53
LI:239245.3:2001JAN12
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53
LI:239245.3:2001JAN12
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53
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53
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53
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53
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53
LI:239245.3:2001JAN12
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53
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53
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53
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53
LI:239245.3:2001JAN12
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53
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53
LI:239245.3:2001JAN12
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2207
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53
LI:239245.3:2001JAN12
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53
LI:239245.3:2001JAN12
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53
LI:239245.3:2001JAN12
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53
LI:239245.3:2001JAN12
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53
LI:239245.3:2001JAN12
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53
LI:239245.3:2001JAN12
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53
LI:239245.3:2001JAN12
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53
LI:239245.3:2001JAN12
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53
LI:239245.3:2001JAN12
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1707

53
LI:239245.3:2001JAN12
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53
LI:239245.3:2001JAN12
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53
LI:239245.3:2001JAN12
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53
LI:239245.3:2001JAN12
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53
LI:239245.3:2001JAN12
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53
LI:239245.3:2001JAN12
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53
LI:239245.3:2001JAN12
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53
LI:239245.3:2001JAN12
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53
LI:239245.3:2001JAN12
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53
LI:239245.3:2001JAN12
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53
LI:239245.3:2001JAN12
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53
LI:239245.3:2001JAN12
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123
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53
LI:239245.3:2001JAN12
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123
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53
LI:239245.3:2001JAN12
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134
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53
LI:239245.3:2001JAN12
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1749
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53
LI:239245.3:2001JAN12
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53
LI:239245.3:2001JAN12
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1760
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53
LI:239245.3:2001JAN12
2842537H1
1757
1878

53
LI:239245.3:2001JAN12
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116
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53
LI:239245.3:2001JAN12
g5865529
2164
2569

53
LI:239245.3:2001JAN12
5216370H1
2165
2416

53
LI:239245.3:2001JAN12
g4452054
2166
2575

53
LI:239245.3:2001JAN12
g5879020
2166
2573

53
LI:239245.3:2001JAN12
826886H1
1530
1847

53
LI:239245.3:2001JAN12
g3736018
2271
2568

53
LI:239245.3:2001JAN12
g2328909
2269
2570

53
LI:239245.3:2001JAN12
g6116973
2290
2556

53
LI:239245.3:2001JAN12
70876454V1
1314
1824

53
LI:239245.3:2001JAN12
5703843H1
1903
2186

53
LI:239245.3:2001JAN12
70876377V1
1903
2355

53
LI:239245.3:2001JAN12
4361570H1
1907
2196

53
LI:239245.3:2001JAN12
7754262H1
862
1205

53
LI:239245.3:2001JAN12
4543041F8
1716
2330

53
LI:239245.3:2001JAN12
4543041H1
1716
1794

53
LI:239245.3:2001JAN12
2527887H1
1720
2070

53
LI:239245.3:2001JAN12
3550484H1
1721
1929

53
LI:239245.3:2001JAN12
70874265V1
1726
2272

53
LI:239245.3:2001JAN12
2737867H1
854
1030

53
LI:239245.3:2001JAN12
4884036F6
471
532

53
LI:239245.3:2001JAN12
7731661J1
810
1430

53
LI:239245.3:2001JAN12
7317594H1
820
1473

53
LI:239245.3:2001JAN12
2657291H1
839
1075

53
LI:239245.3:2001JAN12
4545275H1
847
1030

53
LI:239245.3:2001JAN12
961661R1
853
1381

53
LI:239245.3:2001JAN12
961661H1
853
1102

53
LI:239245.3:2001JAN12
2736351H1
854
1030

53
LI:239245.3:2001JAN12
70875758V1
1831
2165

53
LI:239245.3:2001JAN12
7093989H1
88
397

53
LI:239245.3:2001JAN12
7095177H1
88
397

53
LI:239245.3:2001JAN12
555356H1
92
320

53
LI:239245.3:2001JAN12
70873807V1
1512
1806

53
LI:239245.3:2001JAN12
1298202H1
1512
1726

53
LI:239245.3:2001JAN12
857713R1
1525
2145

53
LI:239245.3:2001JAN12
857713H1
1525
1756

53
LI:239245.3:2001JAN12
2794287H1
1653
1978

53
LI:239245.3:2001JAN12
3885390H2
1655
1957

53
LI:239245.3:2001JAN12
624335H1
1677
1908

53
LI:239245.3:2001JAN12
7748039H1
1694
2261

53
LI:239245.3:2001JAN12
7748046H1
1694
2262

53
LI:239245.3:2001JAN12
70875390V1
1696
2187

53
LI:239245.3:2001JAN12
71077335V1
1699
1932

53
LI:239245.3:2001JAN12
684887H1
1510
1813

53
LI:239245.3:2001JAN12
1256326H1
1510
1679

53
LI:239245.3:2001JAN12
7054670H1
1512
2096

53
LI:239245.3:2001JAN12
1298202F1
1512
1942

53
LI:239245.3:2001JAN12
6310557H1
1767
2439

53
LI:239245.3:2001JAN12
3600715H1
1765
2057

53
LI:239245.3:2001JAN12
2592814H1
1773
2023

53
LI:239245.3:2001JAN12
385678H1
1778
2076

53
LI:239245.3:2001JAN12
4852963H1
1787
2080

53
LI:239245.3:2001JAN12
213146H1
1802
2039

53
LI:239245.3:2001JAN12
207370H1
1802
2028

53
LI:239245.3:2001JAN12
7924721H1
1811
2428

53
LI:239245.3:2001JAN12
g1378507
1829
2118

53
LI:239245.3:2001JAN12
027545H1
1761
1940

53
LI:239245.3:2001JAN12
6310542H1
1767
2382

53
LI:239245.3:2001JAN12
2521749H1
1153
1402

53
LI:239245.3:2001JAN12
g1970688
1169
1477

53
LI:239245.3:2001JAN12
71075977V1
1652
1829

53
LI:239245.3:2001JAN12
71078829V1
1641
1830

53
LI:239245.3:2001JAN12
70874334V1
1661
2081

53
LI:239245.3:2001JAN12
3808662H1
1254
1468

53
LI:239245.3:2001JAN12
7596425H1
1280
1747

53
LI:239245.3:2001JAN12
7596517H1
1287
1487

53
LI:239245.3:2001JAN12
70874514V1
1292
1977

53
LI:239245.3:2001JAN12
7737983J1
1298
1966

53
LI:239245.3:2001JAN12
5641551H1
1219
1460

53
LI:239245.3:2001JAN12
3372035H1
1225
1488

53
LI:239245.3:2001JAN12
2208403F6
1239
1713

53
LI:239245.3:2001JAN12
2208403H1
1239
1468

53
LI:239245.3:2001JAN12
1232232F1
1243
1882

53
LI:239245.3:2001JAN12
1232232H1
1243
1468

53
LI:239245.3:2001JAN12
2097186H1
1254
1350

53
LI:239245.3:2001JAN12
1616965H1
1984
2082

53
LI:239245.3:2001JAN12
4274892H1
1990
2266

53
LI:239245.3:2001JAN12
3217425H1
1998
2285

53
LI:239245.3:2001JAN12
3794510H1
1999
2310

53
LI:239245.3:2001JAN12
71231645V1
2012
2538

53
LI:239245.3:2001JAN12
2917810H1
2018
2191

53
LI:239245.3:2001JAN12
1662812T6
2023
2532

53
LI:239245.3:2001JAN12
g3959977
2025
2208

53
LI:239245.3:2001JAN12
2939339H1
2050
2297

53
LI:239245.3:2001JAN12
71076381V1
2054
2242

53
LI:239245.3:2001JAN12
7618579J1
346
532

53
LI:239245.3:2001JAN12
6585411H1
428
532

53
LI:239245.3:2001JAN12
7735630J1
452
1057

53
LI:239245.3:2001JAN12
4884036H1
471
540

53
LI:239245.3:2001JAN12
5721616H1
1086
1451

53
LI:239245.3:2001JAN12
3009701H1
1086
1290

53
LI:239245.3:2001JAN12
8181792H1
1147
1774

53
LI:239245.3:2001JAN12
7092994H1
88
397

53
LI:239245.3:2001JAN12
71232340V1
1645
2115

53
LI:239245.3:2001JAN12
g1685867
2134
2574

53
LI:239245.3:2001JAN12
g6838404
2149
2568

53
LI:239245.3:2001JAN12
g3883938
2151
2563

53
LI:239245.3:2001JAN12
1617213H1
2156
2373

53
LI:239245.3:2001JAN12
1617284H1
2156
2362

53
LI:239245.3:2001JAN12
g1378402
2158
2565

53
LI:239245.3:2001JAN12
g2907599
2160
2570

53
LI:239245.3:2001JAN12
g1368095
2162
2569

53
LI:239245.3:2001JAN12
7655349H1
955
1249

53
LI:239245.3:2001JAN12
2584851H1
957
1223

53
LI:239245.3:2001JAN12
3290971H1
969
1235

53
LI:239245.3:2001JAN12
1702825H1
972
1172

53
LI:239245.3:2001JAN12
1966577R6
976
1304

53
LI:239245.3:2001JAN12
1966577H1
976
1230

53
LI:239245.3:2001JAN12
2840445H1
1044
1291

53
LI:239245.3:2001JAN12
3371148H1
1071
1340

53
LI:239245.3:2001JAN12
7341833H1
1076
1582

53
LI:239245.3:2001JAN12
g1639712
1079
1419

53
LI:239245.3:2001JAN12
70874892V1
1086
1675

53
LI:239245.3:2001JAN12
1256326F1
1510
1876

53
LI:239245.3:2001JAN12
2846001H1
1631
1931

53
LI:239245.3:2001JAN12
g2011313
1634
2052

53
LI:239245.3:2001JAN12
2846005H1
1631
1933

53
LI:239245.3:2001JAN12
70874202V1
1500
2079

53
LI:239245.3:2001JAN12
g4988929
1504
2008

53
LI:239245.3:2001JAN12
g4080167
1504
1944

53
LI:239245.3:2001JAN12
1954746H1
1505
1758

53
LI:239245.3:2001JAN12
5732588H1
1504
1749

53
LI:239245.3:2001JAN12
4657133H2
1506
1759

53
LI:239245.3:2001JAN12
g3741631
2178
2574

53
LI:239245.3:2001JAN12
7367941H1
2178
2569

53
LI:239245.3:2001JAN12
7334888H1
2182
2572

53
LI:239245.3:2001JAN12
g4997973
2190
2572

53
LI:239245.3:2001JAN12
g3649391
2191
2583

53
LI:239245.3:2001JAN12
7653736H1
863
1030

53
LI:239245.3:2001JAN12
g677683
863
1010

53
LI:239245.3:2001JAN12
3746982H1
863
968

53
LI:239245.3:2001JAN12
3600609H1
863
963

53
LI:239245.3:2001JAN12
923998H1
863
956

53
LI:239245.3:2001JAN12
5066463H1
863
956

53
LI:239245.3:2001JAN12
2820190F6
866
1322

53
LI:239245.3:2001JAN12
2820190H1
866
1084

53
LI:239245.3:2001JAN12
2527015H1
866
1044

53
LI:239245.3:2001JAN12
1662845H1
866
1026

53
LI:239245.3:2001JAN12
1602695H1
866
970

53
LI:239245.3:2001JAN12
908279H1
884
1018

53
LI:239245.3:2001JAN12
g654291
894
1139

53
LI:239245.3:2001JAN12
3190503H1
921
1229

53
LI:239245.3:2001JAN12
3190494H1
921
1159

53
LI:239245.3:2001JAN12
3338674H1
922
1171

53
LI:239245.3:2001JAN12
4916345H1
945
1244

53
LI:239245.3:2001JAN12
1255777H1
950
1194

53
LI:239245.3:2001JAN12
1442744H1
340
532

53
LI:239245.3:2001JAN12
g3277690
2125
2575

53
LI:239245.3:2001JAN12
5648193H1
1975
2413

53
LI:239245.3:2001JAN12
1616909H1
1984
2229

53
LI:239245.3:2001JAN12
210406H1
1958
2142

53
LI:239245.3:2001JAN12
1966577T6
1962
2538

53
LI:239245.3:2001JAN12
5050857H1
1963
2218

53
LI:239245.3:2001JAN12
5873551H1
1913
2211

53
LI:239245.3:2001JAN12
2820190T6
1949
2525

53
LI:239245.3:2001JAN12
978588H1
1951
2252

53
LI:239245.3:2001JAN12
978588R1
1953
2308

53
LI:239245.3:2001JAN12
4202459H1
1889
2166

53
LI:239245.3:2001JAN12
5701154H1
1903
2184

53
LI:239245.3:2001JAN12
7653736J1
235
431

53
LI:239245.3:2001JAN12
1621168H1
206
437

53
LI:239245.3:2001JAN12
7731661H1
155
532

53
LI:239245.3:2001JAN12
4140667H1
182
473

53
LI:239245.3:2001JAN12
7726218H1
191
447

53
LI:239245.3:2001JAN12
7726218J1
192
447

53
LI:239245.3:2001JAN12
7255960H2
144
532

53
LI:239245.3:2001JAN12
g3539348
1
374

53
LI:239245.3:2001JAN12
g3931954
1
369

53
LI:239245.3:2001JAN12
776737H1
68
120

53
LI:239245.3:2001JAN12
1985067H1
76
345

53
LI:239245.3:2001JAN12
70876515V1
1550
2105

53
LI:239245.3:2001JAN12
70874022V1
1571
2180

53
LI:239245.3:2001JAN12
3864706H1
1563
1941

53
LI:239245.3:2001JAN12
70875501V1
1580
1915

53
LI:239245.3:2001JAN12
2102912H1
1590
1864

53
LI:239245.3:2001JAN12
71076168V1
1593
1860

53
LI:239245.3:2001JAN12
71078401V1
1600
2023

53
LI:239245.3:2001JAN12
1300869H1
1601
1870

53
LI:239245.3:2001JAN12
g1685978
1606
1939

53
LI:239245.3:2001JAN12
g2026868
1611
1979

53
LI:239245.3:2001JAN12
6162750H1
1623
2183

53
LI:239245.3:2001JAN12
2597777H1
1618
1922

53
LI:239245.3:2001JAN12
g1373526
1623
2083

53
LI:239245.3:2001JAN12
7182776H1
1625
2192

53
LI:239245.3:2001JAN12
7182777H1
1625
2208

53
LI:239245.3:2001JAN12
7182380H1
1625
2096

53
LI:239245.3:2001JAN12
7182715H1
1625
2164

53
LI:239245.3:2001JAN12
g2279137
2081
2570

53
LI:239245.3:2001JAN12
g2360853
2082
2567

53
LI:239245.3:2001JAN12
878611T1
2084
2526

53
LI:239245.3:2001JAN12
878611R1
2084
2471

53
LI:239245.3:2001JAN12
878611H1
2084
2326

53
LI:239245.3:2001JAN12
g4833713
2092
2569

53
LI:239245.3:2001JAN12
212294H1
2097
2321

53
LI:239245.3:2001JAN12
1696062H1
2078
2301

53
LI:239245.3:2001JAN12
702577H1
1414
1657

53
LI:239245.3:2001JAN12
5732556H1
1467
1726

53
LI:239245.3:2001JAN12
70874813V1
1486
2161

53
LI:239245.3:2001JAN12
70873366V1
1494
2015

53
LI:239245.3:2001JAN12
7746913H1
1378
2004

53
LI:239245.3:2001JAN12
70874721V1
1390
1736

53
LI:239245.3:2001JAN12
70874010V1
1394
1941

53
LI:239245.3:2001JAN12
71231919V1
1404
2088

53
LI:239245.3:2001JAN12
7618579H1
1398
2040

53
LI:239245.3:2001JAN12
4137232H1
1409
1718

53
LI:239245.3:2001JAN12
7736457J1
143
532

53
LI:239245.3:2001JAN12
g2670184
2495
2565

53
LI:239245.3:2001JAN12
2956393H1
2249
2532

53
LI:239245.3:2001JAN12
2955719H1
2249
2531

53
LI:239245.3:2001JAN12
g3932853
2252
2572

53
LI:239245.3:2001JAN12
g3202786
2255
2569

53
LI:239245.3:2001JAN12
g3679306
2256
2563

53
LI:239245.3:2001JAN12
g1994399
2269
2569

53
LI:239245.3:2001JAN12
g1390701
2268
2557

53
LI:239245.3:2001JAN12
2503776H1
2335
2569

53
LI:239245.3:2001JAN12
5326624H1
2311
2562

53
LI:239245.3:2001JAN12
g654218
2327
2575

53
LI:239245.3:2001JAN12
2504103H1
2335
2538

53
LI:239245.3:2001JAN12
g2674844
2404
2583

53
LI:239245.3:2001JAN12
g2563163
2381
2568

53
LI:239245.3:2001JAN12
2519285T6
2395
2633

53
LI:239245.3:2001JAN12
3703849H1
2397
2569

53
LI:239245.3:2001JAN12
1910802T6
2409
2533

53
LI:239245.3:2001JAN12
2883983H1
2433
2569

53
LI:239245.3:2001JAN12
2756734H1
2457
2569

53
LI:239245.3:2001JAN12
g3049728
2487
2563

54
LI:142384.5:2001JAN12
7603466H1
2612
3069

54
LI:142384.5:2001JAN12
g7155580
2612
3039

54
LI:142384.5:2001JAN12
g6641619
2660
3055

54
LI:142384.5:2001JAN12
g7701867
2668
3055

54
LI:142384.5:2001JAN12
7168104H1
2673
3030

54
LI:142384.5:2001JAN12
7692414J1
2702
3007

54
LI:142384.5:2001JAN12
g8008089
2734
3055

54
LI:142384.5:2001JAN12
7957058J1
2516
2933

54
LI:142384.5:2001JAN12
8036889J1
571
1163

54
LI:142384.5:2001JAN12
7400862H1
623
1127

54
LI:142384.5:2001JAN12
7380279H1
675
1246

54
LI:142384.5:2001JAN12
7582606H1
693
1129

54
LI:142384.5:2001JAN12
7720989H1
704
1315

54
LI:142384.5:2001JAN12
8324749J1
765
1190

54
LI:142384.5:2001JAN12
7725609H1
767
1239

54
LI:142384.5:2001JAN12
8002540H1
775
1401

54
LI:142384.5:2001JAN12
7440540H1
560
1148

54
LI:142384.5:2001JAN12
6991082HI
53
274

54
LI:142384.5:2001JAN12
g4195018
56
224

54
LI:142384.5:2001JAN12
g5444909
62
196

54
LI:142384.5:2001JAN12
g4736683
62
531

54
LI:142384.5:2001JAN12
g5765521
62
542

54
LI:142384.5:2001JAN12
g5110384
62
537

54
LI:142384.5:2001JAN12
g5744052
80
524

54
LI:142384.5:2001JAN12
7181281H1
85
634

54
LI:142384.5:2001JAN12
7586630H1
314
807

54
LI:142384.5:2001JAN12
7734637H1
331
842

54
LI:142384.5:2001JAN12
7633218H1
363
621

54
LI:142384.5:2001JAN12
7702987J1
361
573

54
LI:142384.5:2001JAN12
7633218J1
391
620

54
LI:142384.5:2001JAN12
3801178H1
366
564

54
LI:142384.5:2001JAN12
6606927H1
422
806

54
LI:142384.5:2001JAN12
5725556H1
465
939

54
LI:142384.5:2001JAN12
7721053J1
536
1154

54
LI:142384.5:2001JAN12
8002558H1
775
1449

54
LI:142384.5:2001JAN12
7726134J1
782
1004

54
LI:142384.5:2001JAN12
7726134H1
782
1004

54
LI:142384.5:2001JAN12
8081712U1
847
1484

54
LI:142384.5:2001JAN12
8268318H1
847
1301

54
LI:142384.5:2001JAN12
6459774H1
854
1149

54
LI:142384.5:2001JAN12
7717159J1
955
1589

54
LI:142384.5:2001JAN12
7717159H1
1039
1620

54
LI:142384.5:2001JAN12
7621301J1
1069
1705

54
LI:142384.5:2001JAN12
8024879J1
1075
1728

54
LI:142384.5:2001JAN12
7994967H1
1122
1796

54
LI:142384.5:2001JAN12
7693912J2
1137
1670

54
LI:142384.5:2001JAN12
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54
LI:142384.5:2001JAN12
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54
LI:142384.5:2001JAN12
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54
LI:142384.5:2001JAN12
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54
LI:142384.5:2001JAN12
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1994

54
LI:142384.5:2001JAN12
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1931

54
LI:142384.5:2001JAN12
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2203

54
LI:142384.5:2001JAN12
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54
LI:142384.5:2001JAN12
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54
LI:142384.5:2001JAN12
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54
LI:142384.5:2001JAN12
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54
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LI:142384.5:2001JAN12
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LI:142384.5:2001JAN12
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54
LI:142384.5:2001JAN12
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54
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55
LI:2068768.1:2001JAN12
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56
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56
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56
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56
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LI:2118074.1:2001JAN12
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LI:2118074.1:2001JAN12
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56
LI:2118074.1:2001JAN12
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192
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LI:2118074.1:2001JAN12
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56
LI:2118074.1:2001JAN12
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1
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56
LI:2118074.1:2001JAN12
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1
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57
LI:1189068.4:2001JAN12
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LI:1189068.4:2001JAN12
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LI:1189068.4:2001JAN12
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LI:1189068.4:2001JAN12
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57
LI:1189068.4:2001JAN12
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LI:1189068.4:2001JAN12
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57
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LI:1189068.4:2001JAN12
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LI:1189068.4:2001JAN12
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323
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LI:1189068.4:2001JAN12
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325
768

57
LI:1189068.4:2001JAN12
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441
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LI:1189068.4:2001JAN12
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LI:1189068.4:2001JAN12
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LI:1189068.4:2001JAN12
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LI:1189068.4:2001JAN12
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LI:1189068.4:2001JAN12
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57
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57
LI:1189068.4:2001JAN12
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58
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LI:2118704.1:2001JAN12
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58
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58
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58
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LI:2118704.1:2001JAN12
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LI:2118704.1:2001JAN12
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LI:2118704.1:2001JAN12
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58
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LI:031700.2:2001JAN12
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LI:031700.2:2001JAN12
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LI:031700.2:2001JAN12
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LI:2120122.1:2001JAN12
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60
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60
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60
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LI:413584.1:2001JAN12
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LI:413584.1:2001JAN12
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LI:413584.1:2001JAN12
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LI:413584.1:2001JAN12
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738
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LI:413584.1:2001JAN12
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LI:413584.1:2001JAN12
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LI:413584.1:2001JAN12
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LI:413584.1:2001JAN12
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LI:413584.1:2001JAN12
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LI:413584.1:2001JAN12
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LI:413584.1:2001JAN12
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63
LI:413584.1:2001JAN12
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63
LI:413584.1:2001JAN12
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LI:413584.1:2001JAN12
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LI:2122897.2:2001JAN12
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LI:2122897.2:2001JAN12
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761

68
LI:2122897.2;2001JAN12
70601467V1
508
761

68
LI:2122897.2:2001JAN12
4438637F8
508
766

68
LI:2122897.2:2001JAN12
4122257H1
674
761

68
LI:2122897.2:2001JAN12
g4269040
1035
1390

68
LI:2122897.2:2001JAN12
g3424416
1287
1389

68
LI:2122897.2:2001JAN12
8282552T1
902
1153

68
LI:2122897.2:2001JAN12
70602026V1
532
761

68
LI:2122897.2:2001JAN12
3690665F6
494
654

68
LI:2122897.2:2001JAN12
6583638H1
508
652

68
LI:2122897.2:2001JAN12
1653640H1
1105
1321

68
LI:2122897.2:2001JAN12
71741923V1
365
761

68
LI:2122897.2:2001JAN12
1551840H1
500
707

68
LI:2122897.2:2001JAN12
71738610V1
570
701

68
LI:2122897.2:2001JAN12
4438637H1
508
693

68
LI:2122897.2:2001JAN12
5351563H1
508
677

68
LI:2122897.2:2001JAN12
2060566H1
508
672

68
LI:2122897.2:2001JAN12
70599945V1
508
761

68
LI:2122897.2:2001JAN12
g2540873
1027
1391

68
LI:2122897.2:2001JAN12
g1422963
1173
1361

68
LI:2122897.2:2001JAN12
1422495H1
1027
1109

68
LI:2122897.2:2001JANI2
7061305F8
541
761

68
LI:2122897.2:2001JAN12
6597257F6
1027
1389

68
LI:2122897.2:2001JAN12
6597257F8
1027
1309

68
LI:2122897.2:2001JAN12
70601390V1
508
763

68
LI:2122897.2:2001JAN12
71746492V1
204
783

68
LI:2122897.2:2001JAN12
71743705V1
251
783

68
LI:2122897.2:2001JAN12
659903H1
1046
1323

68
LI:2122897.2:2001JAN12
g3050614
1263
1320

68
LI:2122897.2:2001JAN12
70602338V1
679
1112

68
LI:2122897.2:2001JAN12
71742394V1
210
927

68
LI:2122897.2:2001JAN12
71744775V1
201
821

68
LI:2122897.2:2001JAN12
3690665H1
494
795

68
LI:2122897.2:2001JAN12
7001467R8
202
794

68
LI:2122897.2:2001JAN12
7621750H1
237
772

68
LI:2122897.2:2001JAN12
71746378V1
282
786

68
LI:2122897.2:2001JAN12
6597429F8
1027
1402

68
LI:2122897.2:2001JAN12
71744345V1
723
1389

68
LI:2122897.2:2001JAN12
6840505H1
1006
1380

68
LI:2122897.2:2001JAN12
g2335604
958
1363

68
LI:2122897.2:2001JAN12
g892146
1046
1403

68
LI:2122897.2:2001JAN12
1841836H1
1170
1375

68
LI:2122897.2:2001JAN12
g5858210
1027
1390

68
LI:2122897.2:2001JAN12
70601310V1
499
761

68
LI:2122897.2:2001JAN12
2867016H1
1027
1166

68
LI:2122897.2:2001JAN12
2825806T6
1027
1346

68
LI:2122897.2:2001JAN12
70601290V1
1027
1252

68
LI:2122897.2:2001JAN12
1338987T6
1217
1281

68
LI:2122897.2:2001JAN12
2867016T6
1027
1275

68
LI:2122897.2:2001JAN12
6597429T8
1027
1285

68
LI:2122897.2:2001JAN12
6335075T8
1079
1285

68
LI:2122897.2:2001JAN12
3501989T6
1027
1275

68
LI:2122897.2:2001JAN12
g316924
1027
1246

68
LI:2122897.2:2001JAN12
7001467H1
937
1258

68
LI:2122897.2:2001JAN12
7001467F8
596
1258

68
LI:2122897.2:2001JAN12
2357307H1
1000
1240

68
LI:2122897.2:2001JAN12
4893845T8
1027
1216

68
LI:2122897.2:2001JAN12
70597232V1
707
1228

68
LI:2122897.2:2001JAN12
5970773T7
718
1204

68
LI:2122897.2:2001JAN12
70599974V1
508
761

68
LI:2122897.2:2001JAN12
70597746V1
508
761

68
LI:2122897.2:2001JAN12
g890921
984
1370

68
LI:2122897.2:2001JAN12
1997878T6
1133
1349

68
LI:2122897.2:2001JAN12
1919262H1
1077
1349

68
LI:2122897.2:2001JAN12
3690665T6
1027
1358

68
LI:2122897.2:2001JAN12
1225775T6
1027
1346

68
LI:2122897.2:2001JAN12
g3047646
1041
1351

68
LI:2122897.2:2001JAN12
70598341V1
508
761

68
LI:2122897.2:2001JAN12
g4649260
1027
1204

68
LI:2122897.2:2001JAN12
g5528625
983
1204

68
LI:2122897.2:2001JAN12
70598245V1
508
761

68
LI:2122897.2:2001JAN12
7354283H1
1027
1371

69
LI:2053195.3:2001JAN12
g5054453
29
286

69
LI:2053195.3:2001JAN12
g3147156
29
307

69
LI:2053195.3:2001JAN12
1308962H1
1
163

69
LI:2053195.3:2001JAN12
4742155H1
5
171

70
LI:439397.6:2001JAN12
7725467J1
444
1004

70
LI:439397.6:2001JAN12
417346H1
528
696

70
LI:439397.6:2001JAN12
5526237H2
751
1019

70
LI:439397.6:2001JAN12
71022920V1
777
1362

70
LI:439397.6:2001JAN12
70350975D1
804
1210

70
LI:439397.6:2001JAN12
7645980J1
1
608

70
LI:439397.6:2001JAN12
7725467H1
361
1004

71
LI:816379.6:2001JAN12
71862354V1
964
1396

71
LI:816379.6:2001JAN12
71862484V1
965
1396

71
LI:816379.6:2001JAN12
5755024H1
965
1396

71
LI:816379.6:2001JAN12
70514498D1
973
1396

71
LI:816379.6:2001JAN12
837155R1
999
1374

71
LI:816379.6:2001JAN12
70723496V1
1011
1396

71
LI:816379.6:2001JAN12
733063R1
1023
1396

71
LI;816379.6:2001JAN12
057744H1
1202
1392

71
LI:816379.6:2001JAN12
70510238D1
1215
1396

71
LI:816379.6:2001JAN12
70511221V1
1251
1375

71
LI:816379.6:2001JAN12
g4523810
1251
1396

71
LI:816379.6:2001JAN12
5353076H1
1251
1396

71
LI:816379.6:2001JAN12
621158H1
1252
1396

71
LI:816379.6:2001JAN12
621001H1
1252
1396

71
LI:816379.6:2001JAN12
2069960H1
1268
1396

71
LI:816379.6:2001JAN12
611497H1
1312
1396

71
LI:816379.6:2001JAN12
2318093H1
1548
1808

71
LI:816379.6:2001JAN12
2365110H1
1562
1788

71
LI:816379.6:2001JAN12
6541505H1
1563
2122

71
LI:816379.6:2001JAN12
2367584H1
1571
1799

71
LI:816379.6:2001JAN12
5262880H1
1617
1786

71
LI:816379.6:2001JAN12
2364628F6
1728
2154

71
LI:816379.6:2001JAN12
2364628H1
1728
1958

71
LI:816379.6:2001JAN12
2364628T6
1721
2204

71
LI:816379.6:2001JAN12
3562875H1
1762
2058

71
LI:816379.6:2001JAN12
640040H1
1154
1419

71
LI:816379.6:2001JAN12
5394221H1
1150
1405

71
LI:816379.6:2001JAN12
2869942H1
1155
1410

71
LI:816379.6:2001JAN12
2634306H1
1162
1412

71
LI:816379.6:2001JAN12
488003H1
1163
1417

71
LI:816379.6:2001JAN12
g2322646
1172
1608

71
LI:816379.6:2001JAN12
70923704V1
1184
1608

71
LI:816379.6:2001JAN12
2841649H1
1185
1422

71
LI:816379.6:2001JAN12
3034616H1
1188
1396

71
LI:816379.6:2001JAN12
g4175581
1188
1612

71
LI:816379.6:2001JAN12
4596909F6
1189
1375

71
LI:816379.6:2001JAN12
g2874255
1044
1393

71
LI:816379.6:2001JAN12
386476H1
1053
1330

71
LI:816379.6:2001JAN12
6514626H1
1074
1396

71
LI:816379.6:2001JAN12
70433255D1
1088
1396

71
LI:816379.6:2001JAN12
71275888V1
1120
1397

71
LI:816379.6:2001JAN12
71862635V1
950
1396

71
LI:816379.6:2001JAN12
70516131D1
958
1396

71
LI:816379.6:2001JAN12
71862788V1
961
1359

71
LI:816379.6:2001JAN12
2858353H1
1768
2033

71
LI:816379.6:2001JAN12
2961864H1
1772
2047

71
LI:816379.6:2001JAN12
5341535H1
1826
1934

71
LI:816379.6:2001JAN12
g1046751
729
1025

71
LI:816379.6:2001JAN12
71276608V1
771
1165

71
LI:816379.6:2001JAN12
71276635V1
777
1102

71
LI:816379.6:2001JAN12
70924007V1
789
1396

71
LI:816379.6:2001JAN12
71275891V1
794
1259

71
LI:816379.6:2001JAN12
70924234V1
794
1368

71
LI:816379.6:2001JAN12
71276231V1
802
1297

71
LI:816379.6:2001JAN12
5825651H1
817
1394

71
LI:816379.6:2001JAN12
70925679V1
828
1361

71
LI:816379.6:2001JAN12
70924744V1
840
1396

71
LI:816379.6:2001JAN12
70925722V1
843
1359

71
LI:816379.6:2001JAN12
70923524V1
852
1290

71
LI:816379.6:2001JAN12
70924039V1
866
1396

71
LI:816379.6:2001JAN12
7729811J1
879
1375

71
LI:816379.6:2001JAN12
71863033V1
875
1396

71
LI:816379.6:2001JAN12
71862558V1
886
1396

71
LI:816379.6:2001JAN12
71862587V1
922
1396

71
LI:816379.6:2001JAN12
70513587D1
930
1396

71
LI:816379.6:2001JAN12
70516118D1
936
1394

71
LI:816379.6:2001JAN12
8052754J1
1
624

71
LI:816379.6:2001JAN12
7764417J1
118
654

71
LI:816379.6:2001JAN12
7401916H1
190
685

71
LI:816379.6:2001JAN12
70923844V1
346
799

71
LI:816379.6:2001JAN12
70924180V1
346
933

71
LI:816379.6:2001JAN12
70924465V1
346
862

71
LI:816379.6:2001JAN12
70924539V1
346
895

71
LI:816379.6:2001JAN12
71276579V1
346
940

71
LI:816379.6:2001JAN12
70923858V1
346
896

71
LI:816379.6:2001JAN12
1260150F6
346
654

71
LI:816379.6:2001JAN12
1260150H1
346
590

71
LI:816379.6:2001JAN12
70923076V1
491
1036

71
LI:816379.6:2001JAN12
g712423
588
836

71
LI:816379.6:2001JAN12
g703559
588
849

71
LI:816379.6:2001JAN12
71276111V1
595
1199

71
LI:816379.6:2001JAN12
70924950V1
667
1097

71
LI:816379.6:2001JAN12
70925379V1
666
1226

71
LI:816379.6:2001JAN12
7964383H1
690
1267

71
LI:816379.6:2001JAN12
356585R6
724
1104

71
LI:816379.6:2001JAN12
2024316H1
1122
1406

71
LI:816379.6:2001JAN12
g3416935
1144
1396

71
LI:816379.6:2001JAN12
4157360H1
1147
1384

71
LI:816379.6:2001JAN12
4597309H1
1189
1435

71
LI:816379.6:2001JAN12
g1046650
1190
1396

71
LI:816379.6:2001JAN12
1493337H1
1192
1421

72
LI:2123452.4:2001JAN12
1456029T6
6
472

72
LI:2123452.4:2001JAN12
g5546101
191
470

72
LI:2123452.4:2001JAN12
1448389T6
58
469

72
LI:2123452.4:2001JAN12
g1067509
339
447

72
LI:2123452.4:2001JAN12
2928882H1
157
427

72
LI:2123452.4:2001JAN12
1456029F6
6
288

72
LI:2123452.4:2001JAN12
3448555H1
1
194

72
LI:2123452.4:2001JAN12
1456029H1
6
112

73
LI:474559.8:2001JAN12
71120072V1
1
647

74
LI:1089871.1:2001JAN12
70762020V1
1
125

74
LI:1089871.1:2001JAN12
70759980V1
1
704

74
LI:1089871.1:2001JAN12
70757962V1
1
481

74
LI:1089871.1:2001JAN12
2959305F6
1
471

74
LI:1089871.1:2001JAN12
70762245V1
1
554

74
LI:1089871.1:2001JAN12
g1972285
4
165

74
LI:1089871.1:2001JAN12
3887422H1
30
300

74
LI:1089871.1:2001JAN12
70761421V1
121
461

74
LI:1089871.1:2001JAN12
70758433V1
311
843

74
LI:1089871.1:2001JAN12
70757906V1
320
724

74
LI:1089871.1:2001JAN12
70763177V1
371
840

74
LI:1089871.1:2001JAN12
70762620V1
490
872

74
LI:1089871.1:2001JAN12
70761079V1
531
851

74
LI:1089871.1:2001JAN12
70762764V1
531
851

74
LI:1089871.1:2001JAN12
70759582V1
1236
1481

74
LI:1089871.1:2001JAN12
70759021V1
1285
1928

74
LI:1089871.1:2001JAN12
70758815V1
1294
1468

74
LI:1089871.1:2001JAN12
70757721V1
1302
1481

74
LI:1089871.1:2001JAN12
70767224V1
1310
1481

74
LI:1089871.1:2001JAN12
70761857V1
1314
1481

74
LI:1089871.1:2001JAN12
70764826V1
1381
1912

74
LI:1089871.1:2001JAN12
70758307V1
1409
1976

74
LI:1089871.1:2001JAN12
70760140V1
1774
2154

74
LI:1089871.1:2001JAN12
70761329V1
1779
2007

74
LI:1089871.1:2001JAN12
2959305T6
1821
2277

74
LI:1089871.1:2001JAN12
70760716V1
1843
2265

74
LI:1089871.1:2001JAN12
70762468V1
537
851

74
LI:1089871.1:2001JAN12
70758821V1
542
843

74
LI:1089871.1:2001JAN12
70761878V1
551
843

74
LI:1089871.1:2001JAN12
70762741V1
616
851

74
LI:1089871.1:2001JAN12
70757636V1
681
1265

74
LI:1089871.1:2001JAN12
70758209V1
685
851

74
LI:1089871.1:2001JAN12
70761553V1
685
851

74
LI:1089871.1:2001JAN12
70759811V1
685
1251

74
LI:1089871.1:2001JAN12
70761311V1
717
1320

74
LI:1089871.1:2001JAN12
70760042V1
759
1286

74
LI:1089871.1:2001JAN12
70760336V1
781
1320

74
LI:1089871.1:2001JAN12
70760101V1
1132
1481

74
LI:1089871.1:2001JAN12
70760117V1
1158
1484

74
LI:1089871.1:2001JAN12
70760813V1
1158
1315

74
LI:1089871.1:2001JAN12
70757952V1
1158
1374

74
LI:1089871.1:2001JAN12
70759158V1
1158
1394

74
LI:1089871.1:2001JAN12
70760818V1
1158
1394

74
LI:1089871.1:2001JAN12
70757680V1
1158
1467

74
LI:1089871.1:2001JAN12
7Q761293V1
1158
1458

74
LI:1089871.1:2001JAN12
70759646V1
1158
1609

74
LI:1089871.1:2001JAN12
70761118V1
1158
1458

74
LI:1089871.1:2001JAN12
70762739V1
1158
1481

74
LI:1089871.1:2001JAN12
70761840V1
1161
1477

74
LI:1089871.1:2001JAN12
70762279V1
1164
1481

74
LI:1089871.1:2001JAN12
70762802V1
1195
1481

75
LI:289608.1:2001JAN12
4786611H1
1
252

75
LI:289608.1:2001JAN12
5388881F8
111
661

75
LI:289608.1:2001JAN12
5388881H1
111
191

75
LI:289608.1:2001JAN12
5388881T8
113
630

75
LI:289608.1:2001JAN12
4786611F6
1
452

[0325]

5

TABLE 4

SEQ ID NO:
Template ID
Tissue Distribution

1
LI:418914.1:2001JAN12
Sense Organs - 56%, Respiratory System - 24%

2
LI:246108.7:2001JAN12
Nervous System - 54%, Male Genitalia - 23%, Digestive System - 23%

3
LI:204262.2:2001JAN12
Unclassified/Mixed - 16%, Urinary Tract - 13%, Sense Organs - 12%

4
LI:331661.1:2001JAN12
Nervous System - 43%, Endocrine System - 29%, Hemic and Immune System - 21%

5
LI:335074.1:2001JAN12
Exocrine Glands - 86%

6
LI:154608.1:2001JAN12
Urinary Tract - 31%, Nervous System - 31%, Male Genitalia - 23%

7
LI:462889.1:2001JAN12
Embryonic Structures - 75%, Musculoskeletal System - 12%

8
LI:236680.2:2001JAN12
Unclassified/Mixed - 11%, CardiovascularSystem - 11%

9
LI:228186.1:2001JAN12
Sense Organs - 14%, Unclassified/Mixed - 11%

10
LI:721233.1:2001JAN12
Nervous System - 100%

11
LI:291759.2:2001JAN12
Digestive System - 17%, Urinary Tract - 13%, Connective Tissue - 12%

12
LI:292613.17:2001JAN12
Urinary Tract - 29%, Nervous System - 29%, Digestive System - 21%, Male Genitalia - 21%

13
LI:412959.15:2001JAN12
Embryonic Structures - 73%, Urinary Tract - 13%

14
LI:482512.3:2001JAN12
Sense Organs - 32%, Endocrine System - 10%

15
LI:413231.6:2001JAN12
Digestive System - 38%, Respiratory System - 23%, Nervous System - 23%

16
LI:203383.1:2001JAN12
Musculoskeletal System - 36%, Germ Cells - 25%, Connective Tissue - 18%

17
LI:133186.4:2001JAN12
Urinary Tract - 50%, Male Genitalia - 38%, Nervous System - 13%

18
LI:238576.2:2001JAN12
Urinary Tract - 12%, Respiratory System - 12%

19
LI:903914.3:2001JAN12
Unclassified/Mixed - 13%, Skin - 11%, Nervous System - 10%

20
LI:150817.1:2001JAN12
Nervous System - 100%

21
LI:219627.1:2001JAN12
Unclassified/Mixed - 62%, Urinary Tract - 15%, Male Genitalia - 12%

22
LI:197812.4:2001JAN12
Urinary Tract - 100%

23
LI:101525.1:2001JAN12
Cardiovascular System - 91%

24
LI:891123.1:2001JAN12
Musculoskeletal System - 73%, Male Genitalia - 27%

25
LI:813500.1:2001JAN12
Male Genitalia - 46%, Digestive System - 21%, Female Genitalia - 13%, Nervous System - 13%

26
LI:1037251.1:2001JAN12
Sense Organs - 42%, Hemic and Immune System - 13%, Endocrine System - 11%

27
LI:2032187.1:2001JAN12
Hemic and Immune System - 54%, Connective Tissue - 42%

28
LI:347572.1:2001JAN12
CardiovascularSystem - 32%, Digestive System - 28%, Cardiovascular System - 12%

29
LI:007788.1:2001JAN12
Hemic and Immune System - 67%, Nervous System - 33%

30
LI:336872.1:2001JAN12
Embryonic Structures - 40%, Female Genitalia - 27%, Male Genitalia - 17%

31
LI:1143291.1:2001JAN12
Skin - 19%, Urinary Tract - 14%, Stomatognathic System - 12%

32
LI:093477.1:2001JAN12
Unclassified/Mixed - 93%

33
LI:222105.1:2001JAN12
CardiovascularSystem - 12%

34
LI:816737.2:2001JAN12
Female Genitalia - 29%, Hemic and Immune System - 15%, Urinary Tract - 13%

35
LI:475524.1:2001JAN12
Germ Cells - 47%, Liver - 17%

36
LI:383639.1:2001JAN12
Hemic and Immune System - 75%, Respiratory System - 10%

37
LI:814346.1:2001JAN12
Urinary Tract - 31%, Cardiovascular System - 12%, Hemic and Immune System - 11%

38
LI:898195.6:2001JAN12
Respiratory System - 18%, Embryonic Structures - 14%, Liver - 13%

39
LI:210497.2:2001JAN12
Hemic and Immune System - 100%

40
LI:110297.4:2001JAN12
Endocrine System - 20%, Unclassified/Mixed - 12%

41
LI:2051312.1:2001JAN12
Nervous System - 39%, Respiratory System - 18%, Cardiovascular System - 15%,

Female Genitalia - 15%

42
LI:350272.2:2001JAN12
Exocrine Glands - 19%, Cardiovascular System - 12%, Musculoskeletal System - 11%

43
LI:1085472.4:2001JAN12
Urinary Tract - 28%, Stomatognathic System - 20%, Female Genitalia - 14%

44
LI:1190272.1:2001JAN12
Skin - 50%, Nervous System - 11%

45
LI:1086797.1:2001JAN12
Embryonic Structures - 27%, Stomatognathic System - 19%, Digestive System - 16%

46
LI:1144466.1:2001JAN12
Embryonic Structures - 25%, Connective Tissue - 18%, Nervous System - 15%

47
LI:1147914.1:2001JAN12
Connective Tissue - 30%, Musculoskeletal System - 27%, Female Genitalia - 17%

48
LI:758086.1:2001JAN12
Nervous System - 27%, Cardiovascular System - 24%, Female Genitalia - 14%, Hemic and

Immune System - 14%, Exocrine Glands - 14%

49
LI:765245.5:2001JAN12
Pancreas - 18%, Exocrine Glands - 15%, Connective Tissue - 14%

50
LI:335608.2:2001JAN12
Stomatognathic System - 48%, Digestive System - 15%

51
LI:405795.1:2001JAN12
Embryonic Structures - 58%, Female Genitalia - 19%

52
LI:014872.1:2001JAN12
Connective Tissue - 80%

53
LI:239245.3:2001JAN12
Skin - 13%, Sense Organs - 13%, Respiratory System - 13%

54
LI:142384.5:2001JAN12
Stomatognathic System - 21%, Skin - 18%, Musculoskeletal System - 16%

55
LI:2068768.1:2001JAN12
Unclassified/Mixed - 100%

56
LI:2118074.1:2001JAN12
Endocrine System - 52%, Female Genitalia - 37%

57
LI:1189068.4:2001JAN12
Connective Tissue - 29%, Sense Organs - 26%

58
LI:2118704.1:2001JAN12
Sense Organs - 60%, Nervous System - 13%

59
LI:031700.2:2001JAN12
Female Genitalia - 64%, Urinary Tract - 27%

60
LI:2120122.1:2001JAN12
Unclassified/Mixed - 34%, Sense Organs - 23%, Germ Cells - 11%

61
LI:816174.1:2001JAN12
Digestive System - 22%, Male Genitalia - 22%, Exocrine Glands - 22%

62
LI:1189569.11:2001JAN12
Sense Organs - 92%

63
LI:413584.1:2001JAN12
Unclassified/Mixed - 54%, Embryonic Structures - 11%

64
LI:791042.1:2001JAN12
Digestive System - 25%, Urinary Tract - 22%, Embryonic Structures - 20%

65
LI:1167140.1:2001JAN12
Embryonic Structures - 23%, Exocrine Glands - 19%, Nervous System - 12%,

Respiratory System - 12%

66
LI:054831.1:2001JAN12
Digestive System - 60%, Hemic and Immune System - 40%

67
LI:1175083.1:2001JAN12
Germ Cells - 67%, Male Genitalia - 10%

68
LI:2122897.2:2001JAN12
CardiovascularSystem - 28%, Exocrine Glands - 18%, Cardiovascular System - 14%

69
LI:2053195.3:2001JAN12
Digestive System - 38%, Respiratory System - 38%, Hemic and Immune System - 25%

70
LI:439397.6:2001JAN12
Endocrine System - 33%, Exocrine Glands - 28%, Urinary Tract - 22%

71
LI:816379.6:2001JAN12
Hemic and Immune System - 29%, Urinary Tract - 17%, Endocrine System - 16%

72
LI:2123452.4:2001JAN12
Sense Organs - 71%, Embryonic Structures - 16%

74
LI:1089871.1:2001JAN12
Endocrine System - 55%, Female Genitalia - 27%, Hemic and Immune System - 18%

75
LI:289608.1:2001JAN12
Nervous System - 100%

[0326]

6

TABLE 5

SEQ ID NO:
Frame
Length
Start
Stop
GI Number
Probability Score
Annotation

76
1
177
460
990
g16551610
1.00E−11
(AK056259) unnamed protein product

76
1
177
460
990
g9837385
4.00E−07
retinitis pigmentosa GTPase

regulator-like protein

76
1
177
460
990
g16553150
1.00E−06
(AK057442) unnamed protein product

81
2
70
383
592
g12698182
2.00E−15
hypothetical protein

81
2
70
383
592
g7021164
8.00E−14
unnamed protein product

81
2
70
383
592
g16876883
1.00E−10
(BC016722) Unknown

(protein for IMAGE: 4075924)

82
2
239
2
718
g10437745
1.00E−120
unnamed protein product

82
2
239
2
718
g8926320
1.00E−115
corneal wound healing related protein

82
2
239
2
718
g12861811
1.00E−111
putative

83
2
114
362
703
g16751522
2.00E−35
(AB064543) dioxin inducible factor 3

83
2
114
362
703
g12002226
2.00E−32
C3HC4-type zinc finger protein

83
2
114
362
703
g10437296
2.00E−32
unnamed protein product

85
1
151
43
495
g15128221
1.00E−57
contains ESTs AU100786(C50379),

C26898(C50379), ˜similar

to Arabidopsis

thaliana

chromosome

1, F28N24.7˜unknown protein

85
1
151
43
495
g9502415
6.00E−46
Unknown protein

85
1
151
43
495
g15529270
6.00E−46
At1g29250/F28N24_8

86
2
104
569
880
g7770147
6.00E−16
PRO1847

86
2
104
569
880
g10437752
2.00E−14
unnamed protein product

86
2
104
569
880
g6650810
3.00E−14
PRO1902

89
1
85
1486
1740
g12006213
5.00E−32
DC46

92
1
125
196
570
g13938315
8.00E−42
Unknown (protein for MGC: 15634)

94
1
114
472
813
g12859423
2.00E−23
putative

94
1
114
472
813
g15919915
5.00E−23
putative

94
1
114
472
813
g1841551
5.00E−21
G16

95
2
110
1592
1921
g10438620
2.00E−24
unnamed protein product

95
2
110
1592
1921
g10437485
2.00E−23
unnamed protein product

95
2
110
1592
1921
g7020625
5.00E−23
unnamed protein product

96
2
100
1241
1540
g12698192
4.00E−19
hypothetical protein

96
2
100
1241
1540
g6690223
5.00E−13
PRO0470

96
2
100
1241
1540
g1389766
6.00E−11
unknown

99
2
60
1295
1474
g16303798
2.00E−09
(AF416714) unknown

99
2
60
1295
1474
g11493419
2.00E−09
PRO1367

99
2
60
1295
1474
g6690223
2.00E−08
PRO0470

103
2
135
71
475
g14250579
5.00E−07
hypothetical protein PP1628

103
2
135
71
475
g10441903
5.00E−07
unknown

108
2
197
125
715
g434779
1.00E−20
KIAA0112

108
2
197
125
715
g15278392
1.00E−20
homolog of yeast ribosome

biogenesis regulatory

protein RRS1

108
2
197
125
715
g12804751
1.00E−20
Similar to regulator for

ribosome resistance

homolog (S. cerevisiae)

110
2
257
113
883
g14017947
1.00E−27
KIAA1865 protein

110
2
257
113
883
g10636484
1.00E−27
polyglutamine-containing protein

113
1
129
1
387
g2589160
2.00E−60
DCRA

113
1
129
1
387
g2588993
3.00E−55
Dcra

113
1
129
1
387
g13277666
3.00E−55
Down syndrome critical region gene a

116
3
59
240
416
g14598201
4.00E−24
human CLASP-5

116
3
59
240
416
g16550121
3.00E−15
(AK055401) unnamed protein product

116
3
59
240
416
g14597912
3.00E−15
human CLASP-3

118
1
172
1105
1620
g4678717
4.00E−60
hypothetical protein

118
1
172
1105
1620
g3947678
4.00E−60
dJ206D15.3

118
1
172
1105
1620
g12853820
3.00E−17
putative

119
3
214
3
644
g12845866
5.00E−10
putative

121
2
204
116
727
g6841564
9.00E−16
HSPC172

121
2
204
116
727
g6650543
9.00E−16
unknown

121
2
204
116
727
g5531839
9.00E−16
PTD009

122
1
284
1375
2226
g14388466
3.00E−96
hypothetical protein

122
1
284
1375
2226
g14133251
3.00E−96
KIAA1479 protein

122
1
284
1375
2226
g10434456
3.00E−96
unnamed protein product

124
3
81
549
791
g5726235
2.00E−13
unknown protein U5/2

125
2
129
425
811
g14189960
2.00E−28
PRO0764

125
2
129
425
811
g11493463
2.00E−22
PRO2852

125
2
129
425
811
g9280152
6.00E−22
unnamed portein product

126
3
142
3
428
g1526432
3.00E−09
neutral calponin

126
3
142
3
428
g4432964
4.00E−09
h2-calponin

126
3
142
3
428
g51144
5.00E−09
h2-calponin

131
3
206
3
620
g16198439
1.00E−17
hypothetical protein FLJ13855

131
3
206
3
620
g15929470
1.00E−17
hypothetical protein FLJ13855

131
3
206
3
620
g10436290
1.00E−17
unnamed protein product

133
3
171
24
536
g14424725
8.00E−70
hypothetical protein FLJ13055

133
3
171
24
536
g10434892
8.00E−70
unnamed protein product

133
3
171
24
536
g12852801
9.00E−29
putative

135
1
186
460
1017
g13397124
7.00E−17
unnamed protein product

136
3
95
3
287
g5410527
3.00E−15
paracellin-1

138
1
73
55
273
g16549456
1.00E−07
(AK054840) unnamed protein product

138
1
73
55
273
g9437519
5.00E−07
MOST-1

138
1
73
55
273
g6690229
1.00E−06
PRO0483

140
1
103
148
456
g4809026
9.00E−37
suppressor of G2 allele of skp1 homolog

140
1
103
148
456
g15216168
9.00E−37
putative 40-6-3 protein

140
1
103
148
456
g12654187
9.00E−37
suppressor of G2 allele of SKP1,

S. cerevisiae
, homolog of

144
2
247
29
769
g14026730
8.00E−14
homoserine kinase

144
2
247
29
769
g7298468
5.00E−10
CG15164 gene product

144
2
247
29
769
g15075719
7.00E−09
PUTATIVE AMINOTRANSFERASE

PROTEIN

145
2
79
1040
1276
g1911548
2.00E−27
cytochrome c-like polypeptide

147
2
208
155
778
g5106956
4.00E−97
FH1/FH2 domain-containing protein FHOS

147
2
208
155
778
g12697935
4.00E−61
KIAA1695 protein

147
2
208
155
778
g10438624
4.00E−61
unnamed protein product

149
3
73
246
464
g14189976
6.00E−27
PRO2972

149
3
73
246
464
g3415134
1.00E−14
Phyb1

149
3
73
246
464
g12857019
1.00E−14
putative

151
3
158
3
476
g7243081
6.00E−90
KIAA1350 protein

152
3
84
315
566
g288145
1.00E−05
put. ORF

152
3
84
315
566
g6690248
6.00E−05
PRO0657

[0327]

7

TABLE 6

Program
Description
Reference
Parameter Threshold

ABI
A program that removes vector sequences and masks
Applied Biosystems,

FACTURA
ambiguous bases in nucleic acid sequences.
Foster City, CA.

ABI/
A Fast Data Finder useful in
Applied Biosystems,
Mismatch <50%

PARACEL
comparing and annotating amino
Foster City, CA;

FDF
acid or nucleic acid sequences.
Paracel Inc., Pasadena, CA.

ABI
A program that assembles nucleic acid sequences.
Applied Biosystems,

AutoAssembler

Foster City, CA.

BLAST
A Basic Local Alignment Search Tool useful in
Altschul, S.F. et al. (1990)
ESTs: Probability

sequence similarity search for amino acid and nucleic
J. Mol. Biol. 215: 403-410;
value = 1.0E−8

acid sequences. BLAST includes five functions:
Altschul, S.F. et al. (1997)
or less;

blastp, blastn, blastx, tblastn, and tblastx.
Nucleic Acids Res. 25: 3389-3402.
Full Length sequences:

Probability value =

1.0E−10 or less

FASTA
A Pearson and Lipman algorithm that searches for
Pearson, W. R. and
ESTs: fasta E

similarity between a query sequence and a group of
D. J. Lipman (1988) Proc. Natl.
value = 1.06E−6;

sequences of the same type. FASTA comprises as
Acad Sci. USA 85: 2444-2448;
Assembled ESTs: fasta

least five functions: fasta, tfasta, fastx, tfastx, and
Pearson, W. R. (1990) Methods Enzymol. 183: 63-98;
Identity = 95% or

ssearch.
and Smith, T. F. and M. S. Waterman (1981)
greater and

Adv. Appl. Math. 2: 482-489.
Matchlength =

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)
Probability value =

sequence against those in BLOCKS, PRINTS,
Nucleic Acids Res. 19: 6565-6572; Henikoff,
1.0E−3 or less

DOMO, PRODOM, and PFAM databases to search
J. G. and S. Henikoff (1996) Methods

for gene families, sequence homology, and structural
Enzymol. 266: 88-105; and Attwood, T. K. et

fingerprint regions.
al. (1997) J. Chem. Inf. Comput. Sci. 37: 417-424.

HMMER
An algorithm for searching a query sequence against
Krogh, A. et al. (1994) J. Mol. Biol.
PFAM hits:

hidden Markov model (HMM)-based databases of
235: 1501-1531; Sonnhammer, E. L. L. et al.
Probability value =

protein family consensus sequences, such as PFAM,
(1988) Nucleic Acids Res. 26: 320-322;
1.0E−3 or less;

INCY, SMART and TIGRFAM.
Durbin, R. et al. (1998) Our World View, in
Signal peptide hits:

a Nutshell, Cambridge Univ. Press, pp. 1-350.
Score = 0 or greater

ProfileScan
An algorithm that searches for structural and
Gribskov, M. et al. (1988) CABIOS 4: 61-66;
Normalized quality

sequence motifs in protein sequences that match
Gribskov, M. et al. (1989) Methods
score ≧ GCG

sequence patterns defined in Prosite.
Enzymol. 183: 146-159; Bairoch, A. et al.
specified “HIGH”

(1997) Nucleic Acids Res. 25: 217-221.
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. 8: 175-185;

sequencer traces with high sensitivity and probability.
Ewing, B. and P. Green (1998) Genome

Res. 8: 186-194.

Phrap
A Phils Revised Assembly Program including
Smith, T. F. and M. S. Waterman (1981) Adv.
Score = 120 or greater;

SWAT and CrossMatch, programs based on efficient
Appl. Math. 2: 482-489; Smith, T. F. and
Match length =

implementation of the Smith-Waterman algorithm,
M. S. Waterman (1981) J. Mol. Biol. 147: 195-197;
56 or greater

useful in searching sequence homology and
and Green, P., University of

assembling DNA sequences.
Washington, Seattle, WA.

Consed
A graphical tool for viewing and editing Phrap
Gordon, D. et al. (1998) Genome Res. 8: 195-202.

assemblies.

SPScan
A weight matrix analysis program that scans protein
Nielson, H. et al. (1997) Protein Engineering
Score = 3.5 or greater

sequences for the presence of secretory signal
10: 1-6; Claverie, J. M. and S. Audic (1997)

peptides.
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

determine orientation.
(1996) Protein Sci. 5: 363-371.

TMHMMER
A program that uses a hidden Markov model (HMM)
Sonnhammer, E.L. et al. (1998) Proc. Sixth

to delineate transmembrane segments on protein
Intl. Conf. On Intelligent Systems for Mol.

sequences and determine orientation.
Biol., 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
Bairoch, A. et al. (1997) Nucleic Acids Res.

patterns that matched those defined in Prosite.
25: 217-221; Wisconsin Package Program

Manual, version 9, page M51-59, Genetics

Computer Group, Madison, WI.

[0328]

Number	Date	Country
60261865	Jan 2001	US
60261979	Jan 2001	US
60261864	Jan 2001	US
60261981	Jan 2001	US
60263131	Jan 2001	US
60262208	Jan 2001	US
60262164	Jan 2001	US
60262599	Jan 2001	US
60263329	Jan 2001	US
60263063	Jan 2001	US
60262760	Jan 2001	US
60263070	Jan 2001	US
60263066	Jan 2001	US
60263077	Jan 2001	US
60263076	Jan 2001	US
60263074	Jan 2001	US
60263069	Jan 2001	US

Secretory molecules

Information

Publication Number

Date Filed

Date Published

Inventors

CPC

US Classifications

International Classifications

Abstract

Description

Claims

Priority Claims (17)

PCT Information