chrom_info ( chrom VARCHAR(25), start_pt INTEGER, stop_pt INTEGER, species VARCHAR(25), ) repeat_family_info ( family VARCHAR(50) ) repeat_class_info ( class VARCHAR(50) ) repeat_lineage_info ( lineage VARCHAR(50) ) tfbind_info ( factor VARCHAR(25), id VARCHAR(20) ) genes ( id INTEGER, symbol VARCHAR(50), official VARCHAR(1), description VARCHAR(200), type_of_gene VARCHAR(55), chrom VARCHAR(10), start_pt INTEGER, stop_pt INTEGER, orientation VARCHAR(1), cds_start INTEGER, cds_stop INTEGER, function_summary VARCHAR(500), source VARCHAR(10), num_of_exons SMALLINT, evidence VARCHAR(2) ) gene_dbIDs ( id INTEGER, db VARCHAR(50), dbID VARCHAR(50), ) exons ( name VARCHAR(20), chrom VARCHAR(10), start_pt INTEGER, stop_pt INTEGER, gene_id INTEGER, orientation VARCHAR(1), ) conserved_regions ( local_id INTEGER, chrom VARCHAR(10), start_pt INTEGER, stop_pt INTEGER, species VARCHAR(50) min_perc_id SMALLINT, ave_percent_identity DECIMAL(5,2), num_of_segs SMALLINT, ) seq_file ( ID VARCHAR(9), seq_file VARCHAR(500), start_pt INTEGER, stop_pt INTEGER, header VARCHAR(500) ) local_alignments ( chrom VARCHAR(10), start_pt INTEGER, stop_pt INTEGER, score INTEGER, ID INTEGER, orientation VARCHAR(30), species VARCHAR(50), start2 INTEGER, stop2 INTEGER, other_seq VARCHAR(9), ) gap_free_align ( local_id INTEGER, chrom VARCHAR(10), start_pt INTEGER , stop_pt INTEGER , percent_identity SMALLINT, orientation VARCHAR(30), species VARCHAR(50), chrom2 VARCHAR(25), start2 INTEGER, stop2 INTEGER, len GENERATED ALWAYS AS (stop_pt - start_pt + 1), pct_bin GENERATED ALWAYS AS (INTEGER(percent_identity / 10)), ) gene_alias ( gene_id INTEGER, name VARCHAR(100), source VARCHAR(50), ) gene_cdd ( gene_id INTEGER, name VARCHAR(300), domain_acc VARCHAR(50), ) gene_model_prots ( gene_id INTEGER, protein VARCHAR(50), acc_no VARCHAR(50) ) gene_product ( gene_id INTEGER, name VARCHAR(200) ) gene_ontology ( gene_id INTEGER, category VARCHAR(100), term VARCHAR(250), evidence_code VARCHAR(20), source VARCHAR(50), goID VARCHAR(50) ) go_defs_info ( term VARCHAR(200), goID VARCHAR(20), definition VARCHAR(2000), comments VARCHAR(1000) ) evid_code_info ( code VARCHAR(20), description VARCHAR(200) ) snps ( snp_id INTEGER, dbsource VARCHAR(10), chrom VARCHAR(10), start_pt INTEGER, stop_pt INTEGER, ) snp_allele ( snp_id INTEGER , allele VARCHAR(700) , freq DECIMAL(20,19), type_of VARCHAR(50), ) repeats ( name VARCHAR(50), class VARCHAR(50), family VARCHAR(50), strand VARCHAR(1), chrom VARCHAR(10), start_pt INTEGER, stop_pt INTEGER, milliDiv SMALLINT, lineage VARCHAR(30), ) gene_expr ( gene_id INTEGER, tissue VARCHAR(100), dbsource VARCHAR(50) ) gene_disorders ( gene_id INTEGER, disorder VARCHAR(150), pos_by VARCHAR(50) ) tfbinding_sites ( chrom VARCHAR(10), start_pt INTEGER, stop_pt INTEGER, strand VARCHAR(1), score DECIMAL(3,2), id VARCHAR(20) ) conserved_binding_sites ( chrom VARCHAR(10), start_pt INTEGER, stop_pt INTEGER, strand VARCHAR(5), score DECIMAL(3,2), id VARCHAR(20) ) recomb_rate ( chrom VARCHAR(10), start_pt INTEGER, stop_pt INTEGER, name VARCHAR(20), recomb_rate INTEGER, recomb_rateF INTEGER, recomb_rateM INTEGER, source VARCHAR(20), ) CpGislands ( chrom VARCHAR(10), start_pt INTEGER, stop_pt INTEGER, name VARCHAR(50), ) other_genes ( name VARCHAR(255), chrom VARCHAR(10), strand VARCHAR(1), start_pt INTEGER, stop_pt INTEGER, cds_start INTEGER, cds_stop INTEGER, exon_cnt SMALLINT, id INTEGER, track_name VARCHAR(50) ) other_exons ( name SMALLINT, chrom VARCHAR(10), strand VARCHAR(1), start_pt INTEGER, stop_pt INTEGER, gene_id INTEGER ) genename_search ( gene_id INTEGER, names VARCHAR(4000) ) regulatory_potential ( chrom VARCHAR(10), start_pt INTEGER, stop_pt INTEGER, score DECIMAL(4,3), dim_bins GENERATED ALWAYS AS (INTEGER(score)) ) gc_percent ( chrom VARCHAR(10), start_pt INTEGER, stop_pt INTEGER, score DECIMAL(4,1) ) expressionData ( GENEID INTEGER, AFFY VARCHAR(35), Fetal_brain DECIMAL(10,1), Cerebellum DECIMAL(10,1), Whole_Brain DECIMAL(10,1), Cortex DECIMAL(10,1), Caudate_nucleus DECIMAL(10,1), Amygdala DECIMAL(10,1), Thalamus DECIMAL(10,1), Corpus_callosum DECIMAL(10,1), Spinal_cord DECIMAL(10,1), Whole_Blood DECIMAL(10,1), Testis DECIMAL(10,1), Pancreas DECIMAL(10,1), Placenta DECIMAL(10,1), Pituitary_gland DECIMAL(10,1), Thyroid DECIMAL(10,1), Prostate_Cancer DECIMAL(10,1), Prostate DECIMAL(10,1), Ovary DECIMAL(10,1), OVR278E DECIMAL(10,1), OVR278S DECIMAL(10,1), Uterus DECIMAL(10,1), DRG DECIMAL(10,1), Salivary_gland DECIMAL(10,1), Trachea DECIMAL(10,1), Lung DECIMAL(10,1), Thymus DECIMAL(10,1), Spleen DECIMAL(10,1), Adrenal_gland DECIMAL(10,1), Kidney DECIMAL(10,1), Fetal_liver DECIMAL(10,1), Liver DECIMAL(10,1), Heart DECIMAL(10,1), HUVEC DECIMAL(10,1), THYplus DECIMAL(10,1), THYminus DECIMAL(10,1), Myelogenous_k562 DECIMAL(10,1), Lymphoblastic_molt4 DECIMAL(10,1), Burkitts_Daudi DECIMAL(10,1), Burkitts_Raji DECIMAL(10,1), Hep3b DECIMAL(10,1), A2058 DECIMAL(10,1), DOHH2 DECIMAL(10,1), GA10 DECIMAL(10,1), HL60 DECIMAL(10,1), K422 DECIMAL(10,1), Ramos DECIMAL(10,1), WSU DECIMAL(10,1) ) expressionTissue_info ( TissueName VARCHAR(25) ) multiple_aligns ( chrom VARCHAR(25), start_pt INTEGER, stop_pt INTEGER, strand VARCHAR(1), align_id INTEGER, local_id INTEGER, species_build VARCHAR(10), align_builds VARCHAR(50), score DECIMAL(12,5), score_bin INTEGER GENERATED ALWAYS AS (INTEGER(score / 10000)) ) mult_align_segments ( chrom VARCHAR(25), start_pt INTEGER, stop_pt INTEGER, gap_size SMALLINT, local_id INTEGER ) enzyme_info ( enzyme VARCHAR(25), pattern VARCHAR(25) ) restriction_sites ( chrom VARCHAR(10), start_pt INTEGER, stop_pt INTEGER, enzyme VARCHAR(25) ) parallel_aligns ( chrom VARCHAR(10), start_pt INTEGER, stop_pt INTEGER, align VARCHAR(20), repeat VARCHAR(20) ) regulatory_potential_mult ( chrom VARCHAR(10), start_pt INTEGER, stop_pt INTEGER, score DECIMAL(25, 24), score_bin INTEGER GENERATED ALWAYS AS (INTEGER(score * 1000)) ) gene_orthologs ( gene_id INTEGER, species VARCHAR(25), gene_id2 INTEGER, gene_sym VARCHAR(50), chrom VARCHAR(10), start_pt INTEGER, stop_pt INTEGER, protein_identity DECIMAL(5,2), cds_identity DECIMAL(5,2) ) --internal table to keep track of mRNA and EST tables --they are multiple tables with same structure psl_info ( tablename varchar(50), label varchar(50) ) --this used for many tables --human_mrna, human_est, nonhuman_est, nonhuman_mrna, spliced_ests psl ( id INTEGER, matches INTEGER, misMatches INTEGER, repMatches INTEGER, nCount INTEGER, qNumInsert INTEGER, qBaseInsert INTEGER, tNumInsert INTEGER, tBaseInsert INTEGER, strand VARCHAR(2), qchrom VARCHAR(25), qSize INTEGER, qstart_pt INTEGER, qstop_pt INTEGER, chrom VARCHAR(10), chromSize INTEGER, start_pt INTEGER, stop_pt INTEGER, blockCount INTEGER ) --tables to go with above tables psl_block ( psl_id INTEGER, chrom VARCHAR(10), start_pt INTEGER, stop_pt INTEGER, qchrom VARCHAR(25), qstart_pt INTEGER, qstop_pt INTEGER ) --another set of general table types, bed table from UCSC --our tables:tigr_gene_index, unigene bed_info ( tablename VARCHAR(50), label VARCHAR(50), tabtype VARCHAR(50), blocktab VARCHAR(50), xprtab VARCHAR(50) ) bed ( id INTEGER, chrom VARCHAR(10), start_pt INTEGER, stop_pt INTEGER, name VARCHAR(100), score SMALLINT, strand VARCHAR(1), thickStart INTEGER, thickEnd INTEGER, reserved INTEGER, blockCount INTEGER ) bed_blocks ( bed_id INTEGER, chrom VARCHAR(10), start_pt INTEGER, stop_pt INTEGER ) net_aligns ( build VARCHAR(10), level SMALLINT, block VARCHAR(1), chrom VARCHAR(10), start_pt INTEGER, stop_pt INTEGER, strand VARCHAR(1), chrom2 VARCHAR(25), start2 INTEGER, stop2 INTEGER, chainID INTEGER, align_bases INTEGER, score DOUBLE, qOver INTEGER, qDup INTEGER, syn_type VARCHAR(10), N_bases INTEGER, N_bases2 INTEGER, rep_bases INTEGER, rep_bases2 INTEGER, lsrep_bases INTEGER, lsrep_bases2 INTEGER, ancrep_bases INTEGER, ancrep_bases2 INTEGER, trf_bases INTEGER, trf_bases2 INTEGER ) blat_aligns ( id INTEGER, matches INTEGER, misMatches INTEGER, repMatches INTEGER, nCount INTEGER, qNumInsert INTEGER, qBaseInsert INTEGER, tNumInsert INTEGER, tBaseInsert INTEGER, strand VARCHAR(2), species VARCHAR(50), qchrom VARCHAR(25), qSize INTEGER, qstart_pt INTEGER, qstop_pt INTEGER, chrom VARCHAR(10), chromSize INTEGER, start_pt INTEGER, stop_pt INTEGER, blockCount INTEGER ) rnaGene ( chrom VARCHAR(10) NOT NULL, start_pt INTEGER NOT NULL, stop_pt INTEGER NOT NULL, name VARCHAR(50), score DECIMAL(6,1), strand VARCHAR(1) NOT NULL, source VARCHAR(40) NOT NULL, type VARCHAR(20) NOT NULL, fullScore DECIMAL(7,2), isPsuedo INTEGER ) isochore ( chrom VARCHAR(10) NOT NULL, start_pt INTEGER NOT NULL, stop_pt INTEGER NOT NULL, gc_score DECIMAL(4,1) ) --more tables for internal use align_info ( align_type VARCHAR(10), align_id SMALLINT, order_of SMALLINT, species VARCHAR(50), build VARCHAR(25) ) chain_info ( species VARCHAR(25), build VARCHAR(10), chain_file VARCHAR(50) )