| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:60091814-60092363 | Common:10; Rare:198 | ||||
| chr14:60249505-60249641 | Rare:41 | ||||
| chr14:60980982-60981283 | Rare:115 | ||||
| chr14:61695225-61695586 | Common:3; Rare:109 | ||||
| chr14:61762181-61762454 | Common:4; Rare:93 | ||||
| chr14:63543300-63543641 | Common:4; Rare:94 | ||||
| chr14:63641490-63641573 | Rare:16 | ||||
| chr14:63641813-63642162 | Common:5; Rare:113 | ||||
| chr14:63852880-63853066 | Common:1; Rare:74; Clinvar:2; Clinvar (benign):2 | ||||
| chr14:63853128-63853268 | Common:2; Rare:31; Clinvar (benign):1 | ||||
| chr14:64196973-64197061 | Rare:27 | ||||
| chr14:64387996-64388401 | Common:2; Rare:148 | ||||
| chr14:64503614-64503887 | Common:2; Rare:104 | ||||
| chr14:64504574-64504845 | Rare:79 | ||||
| chr14:64505228-64505347 | Rare:28 |