Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:49686708-49686862 | Common:3; Rare:30 | ||||
chr19:50051005-50051147 | Rare:28 | ||||
chr19:50330766-50330997 | Rare:58 | ||||
chr19:50551696-50551974 | Rare:73 | ||||
chr19:50659535-50659590 | Common:1; Rare:13 | ||||
chr19:50660925-50661215 | Common:2; Rare:63 | ||||
chr19:50694192-50694438 | Common:1; Rare:55 | ||||
chr19:50718432-50718525 | Rare:25 | ||||
chr19:50724768-50725249 | Common:2; Rare:169 | ||||
chr19:51354148-51354436 | Common:2; Rare:104; Clinvar:1; Clinvar (benign):4 | ||||
chr19:51354737-51355023 | Common:1; Rare:50 | ||||
chr19:51594380-51594609 | Common:1; Rare:57 | ||||
chr19:51688133-51688486 | Common:2; Rare:50 | ||||
chr19:51688490-51688759 | Common:3; Rare:54 | ||||
chr19:53102673-53102808 | Rare:32 |