ID: 130065849 | ATAC-STARR-seq lymphoblastoid silent region 12901 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38674457..38674566) | | |
ID: 130065848 | ATAC-STARR-seq lymphoblastoid silent region 12900 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38646217..38646336) | | |
ID: 129391174 | MPRA-validated peak4211 silencer [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38685943..38686143) | | |
ID: 129391173 | MPRA-validated peak4208 silencer [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38577732..38577932) | | |
ID: 127893306 | H3K4me1 hESC enhancer GRCh37_chr20:37357057-37357716 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38728414..38729073) | | |
ID: 127893305 | H3K4me1 hESC enhancer GRCh37_chr20:37354984-37355521 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38726341..38726878) | | |
ID: 127893304 | NANOG-H3K4me1 hESC enhancer GRCh37_chr20:37342659-37343160 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38714016..38714517) | | |
ID: 127893303 | H3K27ac hESC enhancer GRCh37_chr20:37236926-37237426 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38608283..38608783) | | |
ID: 127893302 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:37229033-37229574 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38600390..38600931) | | |
ID: 127893301 | H3K27ac hESC enhancer GRCh37_chr20:37193517-37194017 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38564874..38565374) | | |
ID: 127893300 | H3K4me1 hESC enhancer GRCh37_chr20:37189333-37189849 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38560690..38561206) | | |
ID: 125387270 | H3K4me1 hESC enhancer GRCh37_chr20:37355736-37356396 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38727093..38727753) | | |
ID: 120285842 | VISTA enhancer hs2620 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38691862..38693085) | | |
ID: 111365218 | GATA motif-containing MPRA enhancer 112/113 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38666473..38666617) | | |
ID: 100616190 | microRNA 548o-2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38516563..38516632) | | |
ID: 391247 | GINS complex subunit 2 (Psf2 homolog) pseudogene [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38614371..38615532, complement) | | |
ID: 343578 | Rho GTPase activating protein 40 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38601809..38650653) | C20orf95, dJ1100H13.4 | |
ID: 149685 | adipogenin [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38581197..38588463) | SMAF1 | 611396 |
ID: 140761 | ribosomal protein S3 pseudogene 2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38537750..38538459) | RPS3_4_1701, dJ927M24.3 | |
ID: 140679 | solute carrier family 32 member 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38724486..38729372) | DEE114, GEFSP12, VGAT, VIAAT, VIAAT GEFSP12 | 616440 |