ID: 132090135 | Neanderthal introgressed variant-containing enhancer experimental_30226 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (59005204..59005373) | | |
ID: 132090134 | Neanderthal introgressed variant-containing enhancer experimental_30204 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (58965759..58965928) | | |
ID: 132090133 | Neanderthal introgressed variant-containing enhancer experimental_30105 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (58741297..58741466) | | |
ID: 132090132 | Neanderthal introgressed variant-containing enhancer experimental_30091 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (58718717..58718886) | | |
ID: 130008172 | ATAC-STARR-seq lymphoblastoid silent region 4602 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (58921279..58921388) | | |
ID: 130008171 | ATAC-STARR-seq lymphoblastoid silent region 4601 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (58920551..58920660) | | |
ID: 130008170 | ATAC-STARR-seq lymphoblastoid silent region 4600 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (58920051..58920130) | | |
ID: 130008169 | ATAC-STARR-seq lymphoblastoid active region 6570 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (58919401..58919670) | | |
ID: 127824414 | H3K4me1 hESC enhancer GRCh37_chr12:59327314-59327814 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (58933533..58934033) | | |
ID: 127824413 | NANOG hESC enhancer GRCh37_chr12:59318825-59319449 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (58925044..58925668) | | |
ID: 127824412 | H3K4me1 hESC enhancer GRCh37_chr12:59254059-59254582 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (58860277..58860800) | | |
ID: 127824411 | H3K4me1 hESC enhancer GRCh37_chr12:59235169-59235668 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (58841387..58841886) | | |
ID: 126861547 | BRD4-independent group 4 enhancer GRCh37_chr12:59281329-59282528 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (58887547..58888746) | | |
ID: 124902949 | uncharacterized LOC124902949 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (58588284..58590537) | | |
ID: 124629386 | Sharpr-MPRA regulatory region 8919 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (58670687..58670981) | | |
ID: 110121374 | VISTA enhancer hs1468 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (58967849..58970737) | | |
ID: 105369791 | LRIG3 divergent transcript [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (58920704..59130875) | | |
ID: 101927653 | long intergenic non-protein coding RNA 2388 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (58565959..58781716, complement) | | |
ID: 100506869 | uncharacterized LOC100506869 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (58591702..58812669) | | |
ID: 100129227 | ribosomal protein S6 pseudogene 22 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (59020144..59020925) | RPS6_10_1242 | |