ID: 127397437 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:49455091-49455809 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (49417658..49418376) | | |
ID: 127397436 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:49426165-49426934 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (49388732..49389501) | | |
ID: 127397435 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:49424401-49424954 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (49386968..49387521) | | |
ID: 112935946 | Sharpr-MPRA regulatory region 7935 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (49411123..49412635) | | |
ID: 6988 | T cell leukemia translocation altered [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (49412423..49416476) | | 600690 |
ID: 387 | ras homolog family member A [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (49359145..49411976, complement) | ARH12, ARHA, EDFAOB, RHO12, RHOH12 | 165390 |
ID: 275 | aminomethyltransferase [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (49416778..49422473, complement) | GCE, GCE2, GCST, GCVT, NKH | 238310 |