Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:34714538-34714768 | Common:3; Rare:85 | ||||
chr14:34875264-34875547 | Common:1; Rare:103 | ||||
chr14:34982372-34982698 | Common:1; Rare:131 | ||||
chr14:35046089-35046586 | Common:2; Rare:170 | ||||
chr14:35121925-35122699 | Common:4; Rare:218 | ||||
chr14:35292224-35292538 | Common:4; Rare:99; Clinvar:1 | ||||
chr14:35404651-35404854 | Common:2; Rare:77; Clinvar (benign):2 | ||||
chr14:36320586-36320775 | Common:3; Rare:57 | ||||
chr14:37172036-37172119 | Rare:28 | ||||
chr14:37197812-37198082 | Common:3; Rare:92 | ||||
chr14:39114195-39114346 | Common:2; Rare:53 | ||||
chr14:39170203-39170469 | Common:3; Rare:70 | ||||
chr14:39267026-39267403 | Common:2; Rare:122 | ||||
chr14:44961908-44962259 | Common:3; Rare:102 | ||||
chr14:45253078-45253289 | Rare:56 |