| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:39266069-39266233 | Rare:36 | ||||
| chr14:39266397-39266681 | Common:2; Rare:86 | ||||
| chr14:39267010-39267418 | Common:2; Rare:141 | ||||
| chr14:39432418-39432660 | Common:6; Rare:81 | ||||
| chr14:39432868-39433018 | Rare:50 | ||||
| chr14:41606817-41607122 | Common:4; Rare:96 | ||||
| chr14:44961896-44962259 | Common:3; Rare:106 | ||||
| chr14:44962437-44962593 | Rare:65 | ||||
| chr14:45083927-45084174 | Common:1; Rare:96 | ||||
| chr14:45253078-45253323 | Rare:69 | ||||
| chr14:45253443-45253573 | Common:2; Rare:54 | ||||
| chr14:49586298-49586772 | Common:1; Rare:243; Clinvar (benign):1 | ||||
| chr14:49598672-49599031 | Common:2; Rare:137 | ||||
| chr14:49620563-49620837 | Common:2; Rare:114; Clinvar:3 | ||||
| chr14:49693022-49693188 | Common:1; Rare:63 |