ID: 129934052 | ATAC-STARR-seq lymphoblastoid silent region 11616 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (70979007..70979066) | | |
ID: 129934051 | ATAC-STARR-seq lymphoblastoid silent region 11615 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (70978557..70978646) | | |
ID: 129934050 | ATAC-STARR-seq lymphoblastoid active region 16009 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (70977260..70977529) | | |
ID: 129934049 | ATAC-STARR-seq lymphoblastoid silent region 11614 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (70965166..70965275) | | |
ID: 127273631 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:71166475-71167314 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (70939345..70940184) | | |
ID: 127273630 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:71165634-71166474 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (70938504..70939344) | | |
ID: 127273629 | H3K4me1 hESC enhancer GRCh37_chr2:71128841-71129734 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (70901711..70902604) | | |
ID: 127273628 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:71114858-71115508 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (70887728..70888378) | | |
ID: 124906188 | uncharacterized LOC124906188 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (70930303..70930415, complement) | | |
ID: 106480964 | RNA, 7SL, cytoplasmic 160, pseudogene [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (70965584..70965867) | | |
ID: 105374795 | uncharacterized LOC105374795 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (70972729..70984131, complement) | | |
ID: 104355141 | long intergenic non-protein coding RNA 1143 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (70887871..70889984) | | |
ID: 101927750 | ATP6V1B1 antisense RNA 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (70942013..70948611, complement) | | |
ID: 100462866 | elongin C pseudogene 21 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (70955671..70956391, complement) | TCEB1P21 | |
ID: 79998 | ankyrin repeat domain 53 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (70978445..70985499) | | 617009 |
ID: 25806 | ventral anterior homeobox 2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (70900576..70933446) | DRES93 | 604295 |
ID: 525 | ATPase H+ transporting V1 subunit B1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (70935900..70965431) | ATP6B1, DRTA2, RTA1B, VATB, VMA2, VPP3 | 192132 |