ID: 132088881 | Neanderthal introgressed variant-containing enhancer experimental_65660 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (157626739..157626908) | | |
ID: 129937820 | ATAC-STARR-seq lymphoblastoid silent region 14847 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (158105810..158105859) | | |
ID: 129937819 | ATAC-STARR-seq lymphoblastoid active region 20743 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (158097998..158098167) | | |
ID: 129661140 | ReSE screen-validated silencer GRCh37_chr3:157220998-157221232 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (157503209..157503443) | | |
ID: 127399033 | H3K4me1 hESC enhancer GRCh37_chr3:157820715-157821322 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (158102926..158103533) | | |
ID: 127399032 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:157737752-157738378 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (158019963..158020589) | | |
ID: 127399031 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:157217362-157217925 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (157499573..157500136) | | |
ID: 127399030 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:157216797-157217361 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (157499008..157499572) | | |
ID: 127399029 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:156992312-156992853 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (157274523..157275064) | | |
ID: 127399028 | NANOG hESC enhancer GRCh37_chr3:156973526-156974057 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (157255737..157256268) | | |
ID: 126806858 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr3:157751099-157752298 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (158033310..158034509) | | |
ID: 115995530 | CRISPRi-validated cis-regulatory element chr3.4666 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (157534753..157535190) | | |
ID: 114827843 | VISTA enhancer hs2571 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (157247166..157253098) | | |
ID: 110120724 | VISTA enhancer hs638 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (157871437..157872574) | | |
ID: 108449887 | hs1251 and hs1262 enhancers downstream of SHOX2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (158057953..158063431) | | |
ID: 106480847 | RN7SK pseudogene 46 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (157930492..157930725, complement) | | |
ID: 105374179 | uncharacterized LOC105374179 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (157240811..157251050, complement) | | |
ID: 101928236 | uncharacterized LOC101928236 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (157173700..157393946) | | |
ID: 152078 | solute carrier family 66 member 1 like, pseudogene [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (157543312..157601094) | C3orf55, PQLC2L, SLC66A1L, SLC66A2L | |
ID: 79674 | ventricular zone expressed PH domain containing 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (157259742..157503605, complement) | MELT, VEPH | 609594 |