ID: 132089688 | Neanderthal introgressed variant-containing enhancer experimental_108369 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84575172..84575341) | | |
ID: 130001948 | ATAC-STARR-seq lymphoblastoid active region 28505 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84597296..84597505) | | |
ID: 130001947 | ATAC-STARR-seq lymphoblastoid silent region 19984 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84500432..84500501) | | |
ID: 130001946 | ATAC-STARR-seq lymphoblastoid active region 28504 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84296102..84296631) | | |
ID: 130001945 | ATAC-STARR-seq lymphoblastoid active region 28503 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84293845..84293924) | | |
ID: 130001944 | ATAC-STARR-seq lymphoblastoid active region 28502 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84293395..84293454) | | |
ID: 130001943 | ATAC-STARR-seq lymphoblastoid silent region 19983 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84261213..84261272) | | |
ID: 127815051 | NANOG hESC enhancer GRCh37_chr9:87185076-87185832 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84570161..84570917) | | |
ID: 127815050 | H3K27ac hESC enhancer GRCh37_chr9:86991346-86991846 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84376431..84376931) | | |
ID: 127815049 | NANOG hESC enhancer GRCh37_chr9:86891619-86892170 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84276704..84277255) | | |
ID: 127815048 | H3K4me1 hESC enhancer GRCh37_chr9:86787894-86788403 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84172979..84173488) | | |
ID: 127815047 | OCT4-NANOG hESC enhancer GRCh37_chr9:86766071-86767007 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84151156..84152092) | | |
ID: 127815046 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:86595901-86596409 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (83980986..83981494) | | |
ID: 127815045 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:86595393-86595900 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (83980469..83980985) | | |
ID: 126860660 | MED14-independent group 3 enhancer GRCh37_chr9:87127109-87128308 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84512194..84513393) | | |
ID: 126860659 | BRD4-independent group 4 enhancer GRCh37_chr9:86916903-86918102 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84301988..84303187) | | |
ID: 126860658 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr9:86892303-86893502 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84277388..84278587) | | |
ID: 124902192 | uncharacterized LOC124902192 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84443723..84465560) | | |
ID: 124310575 | Sharpr-MPRA regulatory region 11289 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84206214..84206508) | | |
ID: 108281174 | SLC28A3 intron nontranscribed chromatin-defined enhancer [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84356019..84356757) | | |