ID: 132090070 | Neanderthal introgressed variant-containing enhancer experimental_26510 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21969188..21969357) | | |
ID: 130007534 | ATAC-STARR-seq lymphoblastoid active region 6096 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21795417..21795466) | | |
ID: 130007533 | ATAC-STARR-seq lymphoblastoid active region 6094 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21657514..21657763) | | |
ID: 130007532 | ATAC-STARR-seq lymphoblastoid active region 6093 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21657394..21657483) | | |
ID: 127823805 | H3K4me1 hESC enhancer GRCh37_chr12:22093793-22094770 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21940859..21941836) | | |
ID: 127823804 | H3K4me1 hESC enhancer GRCh37_chr12:22052631-22053131 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21899697..21900197) | | |
ID: 127823803 | H3K4me1 hESC enhancer GRCh37_chr12:22052130-22052630 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21899196..21899696) | | |
ID: 127823802 | H3K4me1 hESC enhancer GRCh37_chr12:21926997-21927994 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21774063..21775120) | | |
ID: 127823801 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:21810675-21811203 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21657741..21658323) | | |
ID: 124629328 | H3K4me1 hESC enhancer GRCh37_chr12:21925998-21926996 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21773064..21774062) | | |
ID: 110121489 | VISTA enhancer hs2151 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21891137..21892666) | | |
ID: 105369689 | uncharacterized LOC105369689 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21662313..21829261) | | |
ID: 102724261 | uncharacterized LOC102724261 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21725611..21757870, complement) | | |
ID: 677880 | thioesterase superfamily member 4 pseudogene 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (22008458..22009588) | | |
ID: 10060 | ATP binding cassette subfamily C member 9 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21797389..21941426, complement) | ABC37, ATFB12, CANTU, CMD1O, IDMYS, SUR2 | 601439 |
ID: 3945 | lactate dehydrogenase B [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21635342..21657842, complement) | HEL-S-281, LDH-B, LDH-HD, TRG-5, LDHB | 150100 |
ID: 3764 | potassium inwardly rectifying channel subfamily J member 8 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21764955..21774706, complement) | KIR6.1, uKATP-1 | 600935 |