ID: 127401333 | H3K27ac hESC enhancer GRCh37_chr4:110651344-110652220 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109730188..109731064) | | |
ID: 127401332 | NANOG hESC enhancer GRCh37_chr4:110537978-110538479 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109616822..109617323) | | |
ID: 124900755 | uncharacterized LOC124900755 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109613511..109619117, complement) | | |
ID: 100874455 | HIG1 hypoxia inducible domain family member 1A pseudogene 14 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109673779..109674321) | | |
ID: 100131440 | CDC42 pseudogene 4 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109555108..109555813) | | |
ID: 81579 | phospholipase A2 group XIIA [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109709989..109730070, complement) | GXII, PLA2G12, ROSSY | 611652 |
ID: 55013 | mitochondrial calcium uniporter dominant negative subunit beta [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109560246..109688719) | CCDC109B | 620702 |
ID: 54433 | GAR1 ribonucleoprotein [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109815510..109824737) | NOLA1 | 606468 |
ID: 3426 | complement factor I [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109730982..109801999, complement) | AHUS3, ARMD13, C3BINA, C3b-INA, FI, IF, KAF | 217030 |
ID: 839 | caspase 6 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109664388..109709767, complement) | CSP-6, MCH2, caspase-6 | 601532 |