Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:24093871-24094499 | Common:6; Rare:166; Clinvar (benign):1 | ||||
chr14:24094521-24094836 | Rare:83 | ||||
chr14:24095063-24095872 | Common:3; Rare:163 | ||||
chr14:24113706-24113791 | Common:1; Rare:21 | ||||
chr14:24113874-24114057 | Common:1; Rare:43 | ||||
chr14:24114061-24114856 | Common:2; Rare:177 | ||||
chr14:24114896-24115389 | Common:3; Rare:135 | ||||
chr14:24135860-24136275 | Common:1; Rare:126 | ||||
chr14:24136402-24136567 | Rare:37 | ||||
chr14:24141320-24141932 | Common:3; Rare:157 | ||||
chr14:24146462-24147061 | Common:3; Rare:173 | ||||
chr14:24147112-24147566 | Common:2; Rare:118 | ||||
chr14:24160955-24161406 | Common:2; Rare:86 | ||||
chr14:24161512-24161812 | Common:2; Rare:66 | ||||
chr14:24171999-24172183 | Rare:51 |