Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:38728880-38729154 | Common:2; Rare:77; Clinvar (benign):2 | ||||
chr19:38771815-38771832 | Common:1; Rare:1 | ||||
chr19:38771984-38772091 | Common:1; Rare:10 | ||||
chr19:38845671-38845912 | Common:1; Rare:71 | ||||
chr19:39197843-39198252 | Common:1; Rare:114 | ||||
chr19:39486216-39486463 | Common:2; Rare:89 | ||||
chr19:40687496-40687818 | Common:1; Rare:61 | ||||
chr19:40810769-40810863 | Common:1; Rare:22 | ||||
chr19:41303684-41304145 | Common:2; Rare:114 | ||||
chr19:42286853-42287130 | Rare:94 | ||||
chr19:42287363-42287702 | Rare:98; Clinvar:1 | ||||
chr19:42291417-42291660 | Rare:110; Clinvar:2 | ||||
chr19:42388892-42389120 | Common:2; Rare:55 | ||||
chr19:42396933-42397188 | Common:1; Rare:59 | ||||
chr19:44847613-44847832 | Common:2; Rare:61 |