ID: 132090787 | Neanderthal introgressed variant-containing enhancer experimental_108402 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (87561981..87562150) | | |
ID: 132089693 | Neanderthal introgressed variant-containing enhancer experimental_108410 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (87570139..87570308) | | |
ID: 132089692 | Neanderthal introgressed variant-containing enhancer experimental_108408 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (87568188..87568357) | | |
ID: 132089691 | Neanderthal introgressed variant-containing enhancer experimental_108397 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (87559759..87559928) | | |
ID: 132089690 | Neanderthal introgressed variant-containing enhancer experimental_108388 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (87555834..87556003) | | |
ID: 130001981 | ATAC-STARR-seq lymphoblastoid active region 28523 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (87722446..87722495) | | |
ID: 130001980 | ATAC-STARR-seq lymphoblastoid active region 28522 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (87605468..87605527) | | |
ID: 130001979 | ATAC-STARR-seq lymphoblastoid active region 28521 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (87605368..87605417) | | |
ID: 129662466 | ReSE screen-validated silencer GRCh37_chr9:90308876-90309094 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (87693961..87694179) | | |
ID: 127815092 | H3K4me1 hESC enhancer GRCh37_chr9:90249751-90250336 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (87634836..87635421) | | |
ID: 127815091 | H3K4me1 hESC enhancer GRCh37_chr9:90234560-90235060 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (87619645..87620145) | | |
ID: 127815090 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:90215267-90215860 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (87600352..87600945) | | |
ID: 127815089 | H3K4me1 hESC enhancer GRCh37_chr9:90207629-90208129 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (87592714..87593214) | | |
ID: 127815088 | H3K4me1 hESC enhancer GRCh37_chr9:90186048-90186548 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (87571133..87571633) | | |
ID: 127815087 | H3K4me1 hESC enhancer GRCh37_chr9:90178705-90179204 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (87563790..87564289) | | |
ID: 127815086 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr9:90145230-90146212 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (87530315..87531297) | | |
ID: 126860672 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr9:90328302-90329501 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (87713387..87714586) | | |
ID: 126860671 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr9:90317453-90318652 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (87702538..87703737) | | |
ID: 126860670 | MED14-independent group 3 enhancer GRCh37_chr9:90314444-90315643 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (87699529..87700728) | | |
ID: 124902198 | uncharacterized LOC124902198 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (87751753..87759256, complement) | | |