| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:35121932-35122642 | Common:3; Rare:206 | ||||
| chr14:35292224-35292479 | Common:4; Rare:93; Clinvar:1 | ||||
| chr14:36320580-36320783 | Common:3; Rare:63 | ||||
| chr14:37197821-37198087 | Common:3; Rare:90 | ||||
| chr14:39103120-39103311 | Common:2; Rare:56 | ||||
| chr14:39114156-39114346 | Common:2; Rare:65 | ||||
| chr14:39175002-39175272 | Common:3; Rare:93 | ||||
| chr14:39267053-39267428 | Common:2; Rare:135 | ||||
| chr14:39432420-39432618 | Common:6; Rare:66 | ||||
| chr14:41606823-41607122 | Common:4; Rare:93 | ||||
| chr14:41608155-41608378 | Rare:54 | ||||
| chr14:44961886-44962278 | Common:3; Rare:114 | ||||
| chr14:45083926-45084180 | Common:1; Rare:98 | ||||
| chr14:47674734-47675024 | Common:1; Rare:90 | ||||
| chr14:49586302-49586772 | Common:1; Rare:243; Clinvar (benign):1 |