| ID: 132090032 | Neanderthal introgressed variant-containing enhancer experimental_24921 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114529420..114529589) | | |
| ID: 132090031 | Neanderthal introgressed variant-containing enhancer experimental_24915 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114526269..114526438) | | |
| ID: 129663248 | ReSE screen-validated silencer GRCh37_chr12:115056546-115056730 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114618741..114618925) | | |
| ID: 127825188 | H3K4me1 hESC enhancer GRCh37_chr12:115173261-115174104 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114735456..114736299) | | |
| ID: 127825187 | H3K4me1 hESC enhancer GRCh37_chr12:115138140-115138949 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114700335..114701144) | | |
| ID: 127825186 | H3K4me1 hESC enhancer GRCh37_chr12:115136449-115137301 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114698644..114699496) | | |
| ID: 127825185 | H3K4me1 hESC enhancer GRCh37_chr12:115135594-115136448 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114697789..114698643) | | |
| ID: 127825184 | H3K4me1 hESC enhancer GRCh37_chr12:115134740-115135593 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114696935..114697788) | | |
| ID: 127825183 | NANOG hESC enhancer GRCh37_chr12:115113537-115114038 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114675732..114676233) | | |
| ID: 127825182 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:115109877-115110436 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114672072..114672631) | | |
| ID: 127825181 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:115109316-115109876 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114671511..114672071) | | |
| ID: 127825180 | NANOG hESC enhancer GRCh37_chr12:115079511-115080012 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114641706..114642207) | | |
| ID: 124903026 | uncharacterized LOC124903026 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114621397..114622924) | | |
| ID: 124900329 | small nucleolar RNA SNORA27 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114737704..114737798) | | |
| ID: 121838564 | Sharpr-MPRA regulatory region 166 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114692844..114693138) | | |
| ID: 110120878 | VISTA enhancer hs483 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114685997..114687700) | | |
| ID: 109286556 | TBX3 promoter region [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114684177..114684686) | | |
| ID: 106479190 | RN7SK pseudogene 216 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114504876..114505187, complement) | | |
| ID: 105370000 | TBX3 antisense RNA 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114682292..114767988) | | |
| ID: 105369999 | uncharacterized LOC105369999 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (114733755..114734755, complement) | | |