Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:103682422-103682834 | Common:5; Rare:86 | ||||
chr14:103695967-103696194 | Common:8; Rare:56 | ||||
chr14:104869530-104869662 | Common:1; Rare:23 | ||||
chr14:105093909-105094052 | Rare:33 | ||||
chr15:22494638-22494916 | Common:1; Rare:35 | ||||
chr15:23685712-23685757 | Rare:10 | ||||
chr15:23685846-23686020 | Rare:23 | ||||
chr15:23686183-23686364 | Common:2; Rare:53; Clinvar (benign):1 | ||||
chr15:24908591-24908838 | Common:5; Rare:48 | ||||
chr15:24912442-24912679 | Rare:44 | ||||
chr15:25007414-25007600 | Rare:21 | ||||
chr15:25036006-25036044 | Rare:10 | ||||
chr15:25088779-25088804 | Rare:13 | ||||
chr15:25093854-25093951 | Common:2; Rare:21 | ||||
chr15:25095696-25095773 | Rare:21 |