ID: 132088666 | Neanderthal introgressed variant-containing enhancer experimental_5382 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (223718424..223718593) | | |
ID: 129932572 | ATAC-STARR-seq lymphoblastoid active region 2591 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (223712136..223712185) | | |
ID: 129932571 | ATAC-STARR-seq lymphoblastoid active region 2590 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (223551206..223551265) | | |
ID: 129932570 | ATAC-STARR-seq lymphoblastoid active region 2589 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (223550756..223550805) | | |
ID: 127271667 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:223926031-223926546 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (223738329..223738844) | | |
ID: 127271666 | H3K4me1 hESC enhancer GRCh37_chr1:223921601-223922461 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (223733899..223734759) | | |
ID: 127271665 | H3K4me1 hESC enhancer GRCh37_chr1:223919231-223919826 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (223731529..223732124) | | |
ID: 127271664 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:223915193-223915853 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (223727491..223728151) | | |
ID: 127271663 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:223906461-223907308 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (223718759..223719606) | | |
ID: 127271662 | H3K27ac hESC enhancer GRCh37_chr1:223899927-223900878 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (223712225..223713176) | | |
ID: 127271661 | H3K27ac hESC enhancer GRCh37_chr1:223895561-223896060 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (223707859..223708358) | | |
ID: 127271660 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:223888788-223889634 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (223701086..223701932) | | |
ID: 127271659 | H3K4me1 hESC enhancer GRCh37_chr1:223660470-223660970 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (223487128..223487628) | | |
ID: 127271658 | H3K4me1 hESC enhancer GRCh37_chr1:223567321-223567822 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (223393979..223394480) | | |
ID: 126806027 | MED14-independent group 3 enhancer GRCh37_chr1:223894361-223895560 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (223706659..223707858) | | |
ID: 126806026 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr1:223815955-223817154 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (223628253..223629452) | | |
ID: 106480111 | RNA, U6 small nuclear 1248, pseudogene [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (223690051..223690114) | | |
ID: 106479584 | RNA, U4 small nuclear 57, pseudogene [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (223373822..223373956) | | |
ID: 105373281 | uncharacterized LOC105373281 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (223677818..223707650, complement) | | |
ID: 105373046 | uncharacterized LOC105373046 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (223738462..223741312, complement) | | |