| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:63543287-63543665 | Common:8; Rare:203 | ||||
| chr14:63641380-63641730 | Common:4; Rare:192 | ||||
| chr14:63641773-63642164 | Common:10; Rare:235 | ||||
| chr14:63727320-63727970 | Common:3; Rare:285 | ||||
| chr14:63727948-63728178 | Common:5; Rare:167 | ||||
| chr14:63852854-63853103 | Common:2; Rare:150; Clinvar:5; Clinvar (benign):4 | ||||
| chr14:64338413-64339071 | Common:10; Rare:220 | ||||
| chr14:64387798-64388418 | Common:4; Rare:361 | ||||
| chr14:64503533-64503961 | Common:5; Rare:236 | ||||
| chr14:64503906-64504339 | Common:2; Rare:137 | ||||
| chr14:64504572-64504864 | Rare:165 | ||||
| chr14:64505179-64505369 | Common:2; Rare:88 | ||||
| chr14:64540433-64540742 | Common:3; Rare:137 | ||||
| chr14:64549521-64550021 | Common:6; Rare:153 | ||||
| chr14:64704275-64704652 | Common:5; Rare:137 |