ID: 132089379 | Neanderthal introgressed variant-containing enhancer experimental_91390 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (170304609..170304778) | | |
ID: 129661896 | ReSE screen-validated silencer GRCh37_chr6:170752981-170753211 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (170443893..170444123) | | |
ID: 127408020 | H3K4me1 hESC enhancer GRCh37_chr6:170757529-170758036 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (170448441..170448948) | | |
ID: 127408019 | H3K4me1 hESC enhancer GRCh37_chr6:170749082-170749660 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (170439994..170440572) | | |
ID: 127408018 | H3K4me1 hESC enhancer GRCh37_chr6:170742555-170743054 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (170433467..170433966) | | |
ID: 127408017 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:170712439-170713033 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (170403351..170403945) | | |
ID: 127408016 | NANOG hESC enhancer GRCh37_chr6:170664768-170665298 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (170355680..170356210) | | |
ID: 127408015 | OCT4-H3K4me1 hESC enhancer GRCh37_chr6:170604755-170605382 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (170295667..170296294) | | |
ID: 127408014 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:170576285-170576861 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (170267197..170267773) | | |
ID: 127408013 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:170575708-170576284 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (170266620..170267196) | | |
ID: 126859914 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr6:170695897-170697096 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (170386809..170388008) | | |
ID: 126859913 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr6:170591232-170592431 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (170282144..170283343) | | |
ID: 124906547 | uncharacterized LOC124906547 [Homo sapiens (human)] | | | |
ID: 124901477 | uncharacterized LOC124901477 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (170441731..170447989, complement) | | |
ID: 124901475 | uncharacterized LOC124901475 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (170395586..170400769) | | |
ID: 124901474 | uncharacterized LOC124901474 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (170380147..170393138, complement) | | |
ID: 124901235 | uncharacterized LOC124901235 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (170459331..170463114, complement) | | |
ID: 123881371 | Sharpr-MPRA regulatory region 11687 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (170434121..170434415) | | |
ID: 110121051 | VISTA enhancer hs1310 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (170438007..170439776) | | |
ID: 107986676 | uncharacterized LOC107986676 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (170436232..170441020) | | |