ID: 129934655 | ATAC-STARR-seq lymphoblastoid silent region 11901 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119234660..119234709) | | |
ID: 129934654 | ATAC-STARR-seq lymphoblastoid active region 16446 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119232939..119233138) | | |
ID: 129934653 | ATAC-STARR-seq lymphoblastoid silent region 11900 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119224417..119224486) | | |
ID: 129934652 | ATAC-STARR-seq lymphoblastoid silent region 11899 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119223577..119224356) | | |
ID: 129660796 | ReSE screen-validated silencer GRCh37_chr2:119843263-119843429 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119085687..119085853) | | |
ID: 127274524 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:120013256-120014122 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119255680..119256546) | | |
ID: 127274523 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:120011987-120012930 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119254411..119255354) | | |
ID: 127274522 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:119998175-119998691 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119240599..119241115) | | |
ID: 127274521 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:119997658-119998174 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119240082..119240598) | | |
ID: 127274520 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:119954185-119955022 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119196609..119197446) | | |
ID: 127274519 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:119953346-119954184 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119195770..119196608) | | |
ID: 127274518 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:119914695-119915505 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119157119..119157929) | | |
ID: 127274517 | H3K4me1 hESC enhancer GRCh37_chr2:119892423-119892923 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119134847..119135347) | | |
ID: 127274516 | H3K4me1 hESC enhancer GRCh37_chr2:119891922-119892422 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119134346..119134846) | | |
ID: 127274515 | H3K4me1 hESC enhancer GRCh37_chr2:119870527-119871192 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119112951..119113616) | | |
ID: 126806331 | MED14-independent group 3 enhancer GRCh37_chr2:119975074-119976273 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119217498..119218697) | | |
ID: 126806330 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr2:119868745-119869944 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119111169..119112368) | | |
ID: 122819146 | Sharpr-MPRA regulatory region 13360 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119218873..119219167) | | |
ID: 107985941 | uncharacterized LOC107985941 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119171101..119206649, complement) | | |
ID: 106481050 | RNA, 7SL, cytoplasmic 468, pseudogene [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119169822..119170115) | | |