| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:34875337-34875380 | Rare:17 | ||||
| chr14:34982481-34982682 | Common:1; Rare:85 | ||||
| chr14:35046102-35046511 | Common:2; Rare:141 | ||||
| chr14:35121935-35122787 | Common:4; Rare:241 | ||||
| chr14:35292179-35292495 | Common:5; Rare:111; Clinvar:1 | ||||
| chr14:35404416-35404779 | Common:3; Rare:129; Clinvar:1; Clinvar (benign):5 | ||||
| chr14:39103204-39103280 | Rare:17 | ||||
| chr14:39170164-39170465 | Common:3; Rare:74 | ||||
| chr14:39179121-39179462 | Common:1; Rare:94 | ||||
| chr14:39267075-39267441 | Common:1; Rare:136 | ||||
| chr14:44961886-44962258 | Common:3; Rare:109 | ||||
| chr14:45242608-45242866 | Common:3; Rare:62 | ||||
| chr14:45253051-45253310 | Rare:70 | ||||
| chr14:49598731-49599041 | Common:1; Rare:114 | ||||
| chr14:49620564-49620820 | Common:2; Rare:103; Clinvar:1 |