Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:97936170-97936346 | Rare:54 | ||||
chr9:101326481-101326756 | Common:1; Rare:50 | ||||
chr9:101437921-101438128 | Rare:38 | ||||
chr9:101442391-101442711 | Common:1; Rare:51 | ||||
chr9:101443503-101443610 | Rare:19 | ||||
chr9:104750810-104751144 | Rare:90 | ||||
chr9:104899883-104900016 | Rare:9 | ||||
chr9:104903667-104903968 | Common:3; Rare:67; Clinvar (benign):4 | ||||
chr9:104904528-104904639 | Common:2; Rare:19 | ||||
chr9:104904739-104904868 | Common:3; Rare:24 | ||||
chr9:104906528-104907085 | Common:7; Rare:88 | ||||
chr9:108890799-108890905 | Rare:19 | ||||
chr9:109478828-109478905 | Common:2; Rare:24 | ||||
chr9:114315168-114315398 | Common:1; Rare:43 | ||||
chr9:114318259-114318467 | Rare:32 |