ID: 132088641 | Neanderthal introgressed variant-containing enhancer experimental_3606 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212461027..212461196) | | |
ID: 132088640 | Neanderthal introgressed variant-containing enhancer experimental_3589 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212453611..212453780) | | |
ID: 129932467 | ATAC-STARR-seq lymphoblastoid active region 2504 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212433426..212433515) | | |
ID: 129932466 | ATAC-STARR-seq lymphoblastoid silent region 1795 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212432706..212433265) | | |
ID: 129932465 | ATAC-STARR-seq lymphoblastoid silent region 1794 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212414538..212414597) | | |
ID: 129660486 | ReSE screen-validated silencer GRCh37_chr1:212558425-212558608 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212385083..212385266) | | |
ID: 129388743 | MPRA-validated peak686 silencer [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212364253..212364453) | | |
ID: 127271509 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:212687383-212688110 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212514041..212514768) | | |
ID: 127271508 | H3K4me1 hESC enhancer GRCh37_chr1:212661052-212661590 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212487710..212488248) | | |
ID: 127271507 | H3K4me1 hESC enhancer GRCh37_chr1:212656212-212656712 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212482870..212483370) | | |
ID: 127271506 | H3K4me1 hESC enhancer GRCh37_chr1:212645425-212645925 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212472083..212472583) | | |
ID: 127271505 | H3K4me1 hESC enhancer GRCh37_chr1:212644924-212645424 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212471582..212472082) | | |
ID: 127271504 | H3K4me1 hESC enhancer GRCh37_chr1:212635334-212635848 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212461992..212462506) | | |
ID: 127271503 | H3K4me1 hESC enhancer GRCh37_chr1:212626055-212626874 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212452713..212453532) | | |
ID: 127271502 | H3K27ac hESC enhancer GRCh37_chr1:212541033-212541616 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212367691..212368274) | | |
ID: 127271501 | H3K27ac hESC enhancer GRCh37_chr1:212540447-212541032 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212367105..212367690) | | |
ID: 124904506 | uncharacterized LOC124904506 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212461665..212465947, complement) | | |
ID: 122149494 | Sharpr-MPRA regulatory region 5085 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212467947..212468241) | | |
ID: 115804245 | CRISPRi-validated cis-regulatory element chr1.11595 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212430995..212431282) | | |
ID: 105372908 | uncharacterized LOC105372908 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212506402..212514782, complement) | | |