ID: 132090704 | Neanderthal introgressed variant-containing enhancer experimental_78969 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (37299590..37299759) | | |
ID: 132089133 | Neanderthal introgressed variant-containing enhancer experimental_79062 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (37336039..37336208) | | |
ID: 132089132 | Neanderthal introgressed variant-containing enhancer experimental_78938 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (37278779..37278948) | | |
ID: 132089131 | Neanderthal introgressed variant-containing enhancer experimental_78906 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (37270229..37270398) | | |
ID: 132089130 | Neanderthal introgressed variant-containing enhancer experimental_78898 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (37267084..37267253) | | |
ID: 129992399 | ATAC-STARR-seq lymphoblastoid silent region 15349 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (37686765..37687074) | | |
ID: 129992398 | ATAC-STARR-seq lymphoblastoid silent region 15348 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (37685915..37686584) | | |
ID: 129992397 | ATAC-STARR-seq lymphoblastoid active region 21416 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (37682774..37682823) | | |
ID: 129992396 | ATAC-STARR-seq lymphoblastoid active region 21415 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (37675979..37676188) | | |
ID: 129992395 | ATAC-STARR-seq lymphoblastoid active region 21414 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (37632397..37632446) | | |
ID: 129992394 | ATAC-STARR-seq lymphoblastoid silent region 15347 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (37393031..37393080) | | |
ID: 129992393 | ATAC-STARR-seq lymphoblastoid active region 21413 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (37390003..37390052) | | |
ID: 127400540 | OCT4-NANOG hESC enhancer GRCh37_chr4:37655185-37655838 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (37653563..37654216) | | |
ID: 127400539 | H3K4me1 hESC enhancer GRCh37_chr4:37636677-37637177 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (37635055..37635555) | | |
ID: 127400538 | OCT4-NANOG hESC enhancer GRCh37_chr4:37608503-37609142 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (37606881..37607520) | | |
ID: 127400537 | H3K4me1 hESC enhancer GRCh37_chr4:37591959-37592459 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (37590337..37590837) | | |
ID: 127400536 | H3K4me1 hESC enhancer GRCh37_chr4:37591458-37591958 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (37589836..37590336) | | |
ID: 127400535 | H3K27ac hESC enhancer GRCh37_chr4:37562271-37562772 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (37560649..37561150) | | |
ID: 127400534 | H3K4me1 hESC enhancer GRCh37_chr4:37541047-37541547 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (37539425..37539925) | | |
ID: 126807032 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr4:37667691-37668890 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (37666069..37667268) | | |