Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:24232314-24232792 | Common:8; Rare:110 | ||||
chr14:24232812-24232976 | Common:1; Rare:40 | ||||
chr14:24299722-24299901 | Common:4; Rare:61 | ||||
chr14:24429819-24430089 | Common:2; Rare:59 | ||||
chr14:24442673-24443056 | Common:5; Rare:117 | ||||
chr14:31207651-31207869 | Common:2; Rare:82 | ||||
chr14:31420475-31420757 | Common:4; Rare:93 | ||||
chr14:31561328-31561475 | Common:2; Rare:57; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:32075684-32075872 | Rare:33 | ||||
chr14:32076664-32077084 | Common:3; Rare:125 | ||||
chr14:34462198-34462548 | Common:1; Rare:125 | ||||
chr14:34874892-34875057 | Common:3; Rare:58 | ||||
chr14:34875277-34875646 | Common:1; Rare:119 | ||||
chr14:34982490-34982696 | Common:1; Rare:86 | ||||
chr14:35046035-35046554 | Common:2; Rare:168 |