| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:45253049-45253312 | Rare:72 | ||||
| chr14:45253509-45253624 | Common:1; Rare:47 | ||||
| chr14:49586235-49586772 | Common:1; Rare:267; Clinvar (benign):1 | ||||
| chr14:49598887-49599062 | Common:1; Rare:59 | ||||
| chr14:49620561-49620894 | Common:2; Rare:127; Clinvar:4 | ||||
| chr14:49621231-49621295 | Rare:20 | ||||
| chr14:49635224-49635358 | Common:1; Rare:30; Clinvar (benign):1 | ||||
| chr14:49688193-49688287 | Rare:37 | ||||
| chr14:49767984-49768277 | Common:2; Rare:112 | ||||
| chr14:49892892-49893140 | Rare:107 | ||||
| chr14:50116422-50116712 | Common:1; Rare:143 | ||||
| chr14:50312146-50312376 | Rare:101 | ||||
| chr14:50396794-50397022 | Common:4; Rare:72 | ||||
| chr14:50532461-50532621 | Common:3; Rare:46 | ||||
| chr14:50561120-50561243 | Rare:21 |