Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:61696433-61696701 | Rare:49 | ||||
chr14:61751063-61751365 | Common:1; Rare:93 | ||||
chr14:63531504-63531610 | Common:1; Rare:13 | ||||
chr14:64411106-64411293 | Rare:45; Clinvar (pathogenic):1 | ||||
chr14:64939862-64939884 | Rare:7 | ||||
chr14:65023149-65023311 | Common:2; Rare:26 | ||||
chr14:67269411-67269772 | Rare:58 | ||||
chr14:67388264-67388388 | Rare:32 | ||||
chr14:67615595-67615628 | Common:1; Rare:9 | ||||
chr14:68458988-68459232 | Rare:28 | ||||
chr14:68795236-68795435 | Common:3; Rare:44 | ||||
chr14:68816772-68817008 | Common:1; Rare:57 | ||||
chr14:68937949-68938059 | Rare:19 | ||||
chr14:69385437-69385722 | Common:3; Rare:45 | ||||
chr14:73280594-73280914 | Rare:49 |