| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:39175069-39175305 | Common:4; Rare:84 | ||||
| chr14:39267067-39267448 | Common:2; Rare:141 | ||||
| chr14:39431620-39431664 | Common:1; Rare:13 | ||||
| chr14:39432402-39432657 | Common:6; Rare:88 | ||||
| chr14:44961844-44962292 | Common:3; Rare:135 | ||||
| chr14:45083943-45084174 | Common:1; Rare:92 | ||||
| chr14:45134224-45134293 | Rare:19 | ||||
| chr14:45135757-45135964 | Common:1; Rare:40 | ||||
| chr14:45253059-45253312 | Rare:70 | ||||
| chr14:45253480-45253578 | Common:2; Rare:43 | ||||
| chr14:49586342-49586782 | Common:1; Rare:234 | ||||
| chr14:49598724-49598996 | Common:1; Rare:100 | ||||
| chr14:49620560-49620921 | Common:3; Rare:134; Clinvar:6; Clinvar (benign):1 | ||||
| chr14:49767580-49767711 | Common:2; Rare:42 | ||||
| chr14:49768566-49768589 | Rare:6 |