ID: 132088761 | Neanderthal introgressed variant-containing enhancer experimental_53336 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (156239038..156239207) | | |
ID: 129934944 | ATAC-STARR-seq lymphoblastoid active region 16661 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (156343342..156343401) | | |
ID: 129934943 | ATAC-STARR-seq lymphoblastoid silent region 12018 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (156342322..156342931) | | |
ID: 129934942 | ATAC-STARR-seq lymphoblastoid active region 16659 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (156332903..156332982) | | |
ID: 129934941 | ATAC-STARR-seq lymphoblastoid silent region 12016 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (156332473..156332672) | | |
ID: 129934940 | ATAC-STARR-seq lymphoblastoid active region 16658 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (156309223..156309312) | | |
ID: 129660828 | ReSE screen-validated silencer GRCh37_chr2:157031916-157032139 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (156175404..156175627) | | |
ID: 129388935 | MPRA-validated peak3906 silencer [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (156051513..156051713) | | |
ID: 129388934 | MPRA-validated peak3905 silencer [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (156049063..156049263) | | |
ID: 129388933 | MPRA-validated peak3904 silencer [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (156021423..156021623) | | |
ID: 127275066 | H3K27ac hESC enhancer GRCh37_chr2:157198093-157198646 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (156341581..156342134) | | |
ID: 127275065 | NANOG-H3K27ac hESC enhancer GRCh37_chr2:157197537-157198092 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (156341025..156341580) | | |
ID: 127275064 | H3K27ac hESC enhancer GRCh37_chr2:157190964-157191836 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (156334452..156335324) | | |
ID: 127275063 | H3K27ac hESC enhancer GRCh37_chr2:157149084-157149974 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (156292572..156293462) | | |
ID: 127275062 | H3K4me1 hESC enhancer GRCh37_chr2:156903772-156904272 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (156047260..156047760) | | |
ID: 127275061 | OCT4-NANOG hESC enhancer GRCh37_chr2:156697781-156698549 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (155841269..155842037) | | |
ID: 126806384 | MED14-independent group 3 enhancer GRCh37_chr2:156939984-156941183 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (156083472..156084671) | | |
ID: 124906082 | uncharacterized LOC124906082 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (156347108..156367286) | | |
ID: 110120673 | VISTA enhancer hs411 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (155870069..155871093) | | |
ID: 105373703 | uncharacterized LOC105373703 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (155756065..155914313, complement) | | |