Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:24367878-24368196 | Common:2; Rare:55 | ||||
chr14:24429855-24429980 | Rare:30 | ||||
chr14:24442643-24443023 | Common:6; Rare:121 | ||||
chr14:26597558-26597627 | Rare:8 | ||||
chr14:30559055-30559201 | Common:2; Rare:54 | ||||
chr14:30622209-30622359 | Common:1; Rare:58 | ||||
chr14:31025319-31025653 | Common:2; Rare:74 | ||||
chr14:31207456-31207562 | Rare:31 | ||||
chr14:31420498-31420760 | Common:4; Rare:87 | ||||
chr14:31561277-31561491 | Common:2; Rare:79; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:32076251-32076326 | Rare:22 | ||||
chr14:32076667-32077041 | Common:3; Rare:112 | ||||
chr14:34462224-34462526 | Common:1; Rare:102 | ||||
chr14:34630093-34630246 | Common:5; Rare:72 | ||||
chr14:34875271-34875433 | Rare:64 |