Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:23969852-23969965 | Common:7; Rare:50 | ||||
chr14:24114996-24115293 | Common:2; Rare:83 | ||||
chr14:24141581-24141862 | Rare:60 | ||||
chr14:24146557-24146744 | Rare:64 | ||||
chr14:24195411-24195709 | Common:1; Rare:68 | ||||
chr14:24213074-24213198 | Rare:24 | ||||
chr14:24213444-24213649 | Common:2; Rare:69 | ||||
chr14:24232307-24232656 | Common:8; Rare:84 | ||||
chr14:24232823-24232936 | Common:1; Rare:25 | ||||
chr14:24242596-24242751 | Rare:34; Clinvar:1; Clinvar (benign):1 | ||||
chr14:24271496-24271685 | Common:2; Rare:49 | ||||
chr14:24442767-24442996 | Common:5; Rare:68 | ||||
chr14:30559055-30559216 | Common:2; Rare:62 | ||||
chr14:30622175-30622365 | Common:1; Rare:81 | ||||
chr14:31420528-31420788 | Common:4; Rare:78 |