Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:21073498-21073621 | Rare:24 | ||||
chr14:21200791-21200821 | Rare:4 | ||||
chr14:21203760-21203895 | Common:1; Rare:34 | ||||
chr14:21249212-21249296 | Rare:20 | ||||
chr14:21259528-21259555 | Rare:4 | ||||
chr14:21399989-21400166 | Rare:38; Clinvar (benign):1 | ||||
chr14:21468402-21468718 | Common:1; Rare:73 | ||||
chr14:22771036-22771372 | Common:2; Rare:118 | ||||
chr14:22844424-22844731 | Rare:84 | ||||
chr14:23058365-23058657 | Common:1; Rare:84 | ||||
chr14:23059507-23059519 | Rare:1 | ||||
chr14:23068867-23068946 | Rare:15 | ||||
chr14:23075565-23075638 | Rare:11 | ||||
chr14:23308528-23308967 | Rare:79 | ||||
chr14:24169562-24169728 | Rare:33 |