ID: 866 | serpin family A member 6 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (94304248..94323336, complement) | CBG | 122500 |
ID: 2099 | estrogen receptor 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (151656672..152129619) | ER, ESR, ESRA, ESTRR, Era, NR3A1 | 133430 |
ID: 6532 | solute carrier family 6 member 4 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (30194319..30235697, complement) | 5-HTT, 5-HTTLPR, 5HTT, HTT, OCD1, SERT, SERT1, hSERT | 182138 |
ID: 5265 | serpin family A member 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (94376747..94390635, complement) | A1A, A1AT, AAT, PI, PI1, PRO2275, alpha1AT, nNIF | 107400 |
ID: 2335 | fibronectin 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (215360865..215436068, complement) | CIG, ED-B, FINC, FN, FNZ, GFND, GFND2, LETS, MSF, SMDCF | 135600 |
ID: 3115 | major histocompatibility complex, class II, DP beta 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (33075990..33089696) | DPB1, HLA-DP, HLA-DP1B, HLA-DPB | 142858 |
ID: 5176 | serpin family F member 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (1762060..1777565) | EPC-1, OI12, OI6, PEDF, PIG35 | 172860 |
ID: 121278 | tryptophan hydroxylase 2 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (71938845..72032440) | ADHD7, NTPH | 607478 |
ID: 3169 | forkhead box A1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (37589552..37595249, complement) | HNF3A, TCF3A | 602294 |
ID: 3170 | forkhead box A2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (22580998..22585490, complement) | HNF-3-beta, HNF3B, TCF3B | 600288 |
ID: 1284 | collagen type IV alpha 2 chain [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (110307284..110513209) | BSVD2, ICH, POREN2 | 120090 |
ID: 1690 | cochlin [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (30874559..30895615) | COCH-5B25B2, DFNA9, DFNB110, COCH | 603196 |
ID: 3843 | importin 5 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (97953675..98024296) | IMB3, KPNB3, Pse1, RANBP5, imp5 | 602008 |
ID: 5655 | kallikrein related peptidase 10 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (51012739..51020097, complement) | NES1, PRSSL1 | 602673 |
ID: 5066 | peptidylglycine alpha-amidating monooxygenase [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (102754783..103031105) | PAL-1, PHM, PAM | 170270 |
ID: 10609 | prolyl 3-hydroxylase family member 4 (inactive) [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41801953..41811949, complement) | LEPREL4, NO55, NOL55, SC65 | 617419 |
ID: 7485 | guided entry of tail-anchored proteins factor 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39380326..39428528) | CHD5, WRB | 602915 |
ID: 200895 | dihydrofolate reductase 2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (94057922..94063320, complement) | DHFRL1, DHFRP4 | 616588 |
ID: 79006 | meteorin, glial cell differentiation regulator [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (715118..719655) | C16orf23, c380A1.2 | 610998 |
ID: 29035 | HUWE1 associated protein modifying stress responses [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (9091644..9121635) | C16orf72, PRO0149, TAPR1 | |