ID: 132090155 | Neanderthal introgressed variant-containing enhancer experimental_31616 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (105454219..105454388) | | |
ID: 130010087 | ATAC-STARR-seq lymphoblastoid active region 7979 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (105177362..105177411) | | |
ID: 130010086 | ATAC-STARR-seq lymphoblastoid silent region 5488 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (105166044..105166093) | | |
ID: 130010085 | ATAC-STARR-seq lymphoblastoid active region 7978 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (105139851..105140260) | | |
ID: 130010084 | ATAC-STARR-seq lymphoblastoid active region 7977 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (105139591..105139800) | | |
ID: 129663378 | ReSE screen-validated silencer GRCh37_chr13:105926712-105926889 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (105274361..105274538) | | |
ID: 127826829 | OCT4-NANOG hESC enhancer GRCh37_chr13:106469046-106469979 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (105816697..105817630) | | |
ID: 127826828 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:106034971-106035756 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (105382621..105383406) | | |
ID: 127826827 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:106034184-106034970 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (105381834..105382620) | | |
ID: 127826826 | OCT4-NANOG hESC enhancer GRCh37_chr13:105934754-105935689 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (105282403..105283338) | | |
ID: 127826825 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr13:105931493-105931993 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (105279142..105279642) | | |
ID: 127826824 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr13:105930992-105931492 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (105278641..105279141) | | |
ID: 127826823 | OCT4-NANOG hESC enhancer GRCh37_chr13:105760089-105760627 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (105107738..105108276) | | |
ID: 126861836 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr13:105998132-105999331 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (105345781..105346980) | | |
ID: 124903244 | uncharacterized LOC124903244 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (105904743..105909706) | | |
ID: 110121473 | VISTA enhancer hs1991 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (105115722..105119547) | | |
ID: 110120930 | VISTA enhancer hs759 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (105363248..105364577) | | |
ID: 107984609 | uncharacterized LOC107984609 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (104999320..105007434, complement) | | |
ID: 105370345 | uncharacterized LOC105370345 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (105572076..105706856, complement) | | |
ID: 105370344 | uncharacterized LOC105370344 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (105410816..105414224) | | |