ID: 132088644 | Neanderthal introgressed variant-containing enhancer experimental_3744 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212569248..212569417) | | |
ID: 129932474 | ATAC-STARR-seq lymphoblastoid silent region 1801 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212636815..212636934) | | |
ID: 129932473 | ATAC-STARR-seq lymphoblastoid silent region 1800 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212609403..212609582) | | |
ID: 129932472 | ATAC-STARR-seq lymphoblastoid silent region 1797 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212606853..212607032) | | |
ID: 129932471 | ATAC-STARR-seq lymphoblastoid active region 2509 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212586616..212586745) | | |
ID: 129932470 | ATAC-STARR-seq lymphoblastoid active region 2508 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212567459..212567508) | | |
ID: 129932469 | ATAC-STARR-seq lymphoblastoid active region 2507 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212566899..212567008) | | |
ID: 129932468 | ATAC-STARR-seq lymphoblastoid active region 2506 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212559237..212559376) | | |
ID: 127271515 | H3K4me1 hESC enhancer GRCh37_chr1:212819605-212820114 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212646263..212646772) | | |
ID: 127271514 | H3K4me1 hESC enhancer GRCh37_chr1:212803852-212804383 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212630510..212631041) | | |
ID: 127271513 | H3K4me1 hESC enhancer GRCh37_chr1:212799247-212799747 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212625905..212626405) | | |
ID: 127271512 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:212781729-212782686 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212608387..212609392) | | |
ID: 127271511 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:212780771-212781728 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212607429..212608386) | | |
ID: 127271510 | H3K27ac hESC enhancer GRCh37_chr1:212731832-212732569 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212558490..212559227) | | |
ID: 127271509 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:212687383-212688110 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212514041..212514768) | | |
ID: 126806003 | BRD4-independent group 4 enhancer GRCh37_chr1:212810785-212811984 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212637443..212638642) | | |
ID: 122149495 | Sharpr-MPRA regulatory region 14805 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212621627..212621921) | | |
ID: 112577538 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr1:212769225-212770424 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212595883..212597082) | | |
ID: 110121257 | VISTA enhancer hs2089 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212531404..212533951) | | |
ID: 105372908 | uncharacterized LOC105372908 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212506402..212514782, complement) | | |