| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:38256051-38256237 | Common:1; Rare:52 | ||||
| chr14:39103713-39103786 | Common:1; Rare:11 | ||||
| chr14:39170249-39170451 | Common:3; Rare:53 | ||||
| chr14:39175081-39175392 | Common:3; Rare:113 | ||||
| chr14:39267044-39267422 | Common:2; Rare:133 | ||||
| chr14:39432122-39432187 | Common:2; Rare:29 | ||||
| chr14:39432418-39432637 | Common:6; Rare:74 | ||||
| chr14:44897065-44897295 | Rare:82 | ||||
| chr14:44961887-44962278 | Common:3; Rare:114 | ||||
| chr14:44962495-44962795 | Rare:100 | ||||
| chr14:45083947-45084180 | Common:1; Rare:92 | ||||
| chr14:45109976-45110138 | Common:3; Rare:33 | ||||
| chr14:45253054-45253453 | Common:1; Rare:116 | ||||
| chr14:49586045-49586333 | Common:3; Rare:96; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr14:49598690-49599047 | Common:2; Rare:133 |