ID: 127460263 | H3K27ac hESC enhancer GRCh37_chr8:125487577-125488120 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (124475336..124475879) | | |
ID: 127460262 | H3K27ac hESC enhancer GRCh37_chr8:125487031-125487576 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (124474790..124475335) | | |
ID: 127460261 | H3K27ac hESC enhancer GRCh37_chr8:125486486-125487030 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (124474245..124474827) | | |
ID: 127460260 | H3K4me1 hESC enhancer GRCh37_chr8:125483735-125484236 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (124471494..124471995) | | |
ID: 127460259 | H3K4me1 hESC enhancer GRCh37_chr8:125452571-125453070 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (124440330..124440829) | | |
ID: 101927612 | RNF139 divergent transcript [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (124462493..124474563, complement) | RNF139-AS1 | |
ID: 55039 | tRNA methyltransferase 12 homolog [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (124450820..124453026) | TRM12, TYW2 | 611244 |
ID: 11236 | ring finger protein 139 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (124474880..124488618) | HRCA1, RCA1, TRC8 | 603046 |