Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:150582546-150582846 | Common:2; Rare:59 | ||||
chr4:150582867-150583164 | Rare:68 | ||||
chr4:150583320-150583692 | Rare:82 | ||||
chr4:150583789-150584116 | Rare:79 | ||||
chr4:151100797-151101006 | Rare:46 | ||||
chr4:151176568-151176949 | Common:1; Rare:46 | ||||
chr4:153684143-153684290 | Common:1; Rare:49 | ||||
chr4:168835986-168836027 | Rare:6 | ||||
chr4:168854675-168854861 | Rare:28 | ||||
chr4:168904953-168905001 | Rare:6 | ||||
chr4:168924139-168924428 | Rare:68; Clinvar:4; Clinvar (benign):1 | ||||
chr4:173508023-173508150 | Rare:33 | ||||
chr4:173508177-173508524 | Common:2; Rare:52 | ||||
chr4:173509545-173509690 | Common:1; Rare:37 | ||||
chr4:173518147-173518251 | Rare:32 |