| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50561124-50561206 | Rare:15 | ||||
| chr14:50668295-50668560 | Common:4; Rare:98 | ||||
| chr14:50912009-50912245 | Rare:58; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr14:50944329-50944596 | Common:4; Rare:98; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:51095071-51095393 | Common:4; Rare:134 | ||||
| chr14:51240154-51240319 | Rare:80 | ||||
| chr14:51651619-51651984 | Common:4; Rare:102 | ||||
| chr14:51860549-51860790 | Rare:67 | ||||
| chr14:51999438-51999796 | Common:2; Rare:71 | ||||
| chr14:52003917-52004439 | Common:3; Rare:186 | ||||
| chr14:52011597-52011805 | Rare:80 | ||||
| chr14:52068996-52069226 | Common:2; Rare:52 | ||||
| chr14:52314053-52314389 | Common:3; Rare:87 | ||||
| chr14:52695509-52695839 | Common:1; Rare:94 | ||||
| chr14:52707055-52707247 | Common:1; Rare:85 |