Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:24242268-24242397 | Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
chr14:24242539-24242720 | Common:1; Rare:41; Clinvar:1; Clinvar (benign):3 | ||||
chr14:24299738-24299871 | Common:4; Rare:36 | ||||
chr14:24429855-24429974 | Rare:28 | ||||
chr14:24442659-24443013 | Common:5; Rare:116 | ||||
chr14:25049901-25050208 | Common:2; Rare:96 | ||||
chr14:26597543-26597681 | Rare:17 | ||||
chr14:29927457-29927711 | Common:2; Rare:63 | ||||
chr14:31025618-31025656 | Rare:12 | ||||
chr14:31207473-31207840 | Common:2; Rare:123 | ||||
chr14:31208137-31208283 | Common:1; Rare:35 | ||||
chr14:31420524-31420737 | Common:3; Rare:66 | ||||
chr14:32076676-32077051 | Common:3; Rare:110 | ||||
chr14:34462214-34462525 | Common:1; Rare:107 | ||||
chr14:34714538-34714854 | Common:5; Rare:125 |