ID: 129992670 | ATAC-STARR-seq lymphoblastoid silent region 15476 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (73258490..73258889) | | |
ID: 129992669 | ATAC-STARR-seq lymphoblastoid active region 21608 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (73039030..73039089) | | |
ID: 127400976 | OCT4-NANOG hESC enhancer GRCh37_chr4:74235125-74235832 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (73369408..73370115) | | |
ID: 127400975 | OCT4-NANOG hESC enhancer GRCh37_chr4:74209023-74209524 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (73343306..73343807) | | |
ID: 127400974 | H3K4me1 hESC enhancer GRCh37_chr4:74205305-74205804 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (73339588..73340087) | | |
ID: 127400973 | H3K4me1 hESC enhancer GRCh37_chr4:74204803-74205304 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (73339086..73339587) | | |
ID: 127400972 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:74124568-74125164 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (73258851..73259447) | | |
ID: 127400971 | H3K4me1 hESC enhancer GRCh37_chr4:74121667-74122167 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (73255950..73256450) | | |
ID: 127400970 | H3K27ac hESC enhancer GRCh37_chr4:73935268-73935784 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (73069485..73070067) | | |
ID: 127400969 | H3K27ac hESC enhancer GRCh37_chr4:73934752-73935267 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (73069035..73069550) | | |
ID: 126807076 | BRD4-independent group 4 enhancer GRCh37_chr4:74191462-74192661 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (73325745..73326944) | | |
ID: 124906432 | uncharacterized LOC124906432 [Homo sapiens (human)] | | | |
ID: 124900713 | uncharacterized LOC124900713 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (73104345..73110740) | | |
ID: 124900180 | small nucleolar RNA SNORA3/SNORA45 family [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (73263960..73264084) | | |
ID: 123477756 | Sharpr-MPRA regulatory region 13076 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (73028672..73028966) | | |
ID: 112268467 | uncharacterized LOC112268467 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (73069946..73071822) | | |
ID: 111832671 | albumin (ALB) 5' regulatory region [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (73397685..73404342) | | |
ID: 102724832 | ANKRD17 divergent transcript [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (73259166..73359023) | | |
ID: 100151688 | RNA, U6atac small nuclear 5, pseudogene [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (73026748..73026872) | | |
ID: 285521 | cytochrome c oxidase assembly factor COX18 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (73052362..73069759, complement) | COX18HS, OXA1L2 | 610428 |