ID: 132090071 | Neanderthal introgressed variant-containing enhancer experimental_26529 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (22188559..22188728) | | |
ID: 132090070 | Neanderthal introgressed variant-containing enhancer experimental_26510 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21969188..21969357) | | |
ID: 130007536 | ATAC-STARR-seq lymphoblastoid silent region 4287 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (22121378..22121437) | | |
ID: 130007535 | ATAC-STARR-seq lymphoblastoid active region 6097 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (22101841..22101980) | | |
ID: 127823808 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:22289754-22290362 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (22136820..22137428) | | |
ID: 127823807 | OCT4-NANOG hESC enhancer GRCh37_chr12:22201245-22201850 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (22048311..22048916) | | |
ID: 127823806 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:22199579-22200284 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (22046645..22047350) | | |
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: 112163548 | Sharpr-MPRA regulatory region 13841 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (22046035..22046471) | | |
ID: 110121489 | VISTA enhancer hs2151 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21891137..21892666) | | |
ID: 107984497 | sulfotransferase family 6B member 2, pseudogene [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (22104493..22140048, complement) | | |
ID: 107048983 | RNA, U1 small nuclear 149, pseudogene [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (22195469..22195629, complement) | | |
ID: 105369690 | uncharacterized LOC105369690 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (22063773..22082527, complement) | | |
ID: 105369689 | uncharacterized LOC105369689 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21662313..21829261) | | |
ID: 677880 | thioesterase superfamily member 4 pseudogene 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (22008458..22009588) | | |
ID: 55907 | cytidine monophosphate N-acetylneuraminic acid synthetase [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (22046218..22065668) | CSS | 603316 |
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: 6489 | ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (22193391..22334707, complement) | GD3S, SIAT8, SIAT8-A, SIAT8A, ST8SiaI | 601123 |