| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:64540417-64540593 | Common:1; Rare:48 | ||||
| chr14:67359765-67360030 | Rare:87 | ||||
| chr14:67674576-67674953 | Common:1; Rare:99 | ||||
| chr14:67816578-67816758 | Rare:31 | ||||
| chr14:68979197-68979559 | Common:2; Rare:109 | ||||
| chr14:69398248-69398430 | Common:1; Rare:72 | ||||
| chr14:69398595-69398716 | Rare:30 | ||||
| chr14:70416959-70417124 | Rare:51 | ||||
| chr14:71320253-71320479 | Rare:68 | ||||
| chr14:73027054-73027399 | Common:2; Rare:89 | ||||
| chr14:73058357-73058566 | Common:2; Rare:62 | ||||
| chr14:73950039-73950333 | Common:6; Rare:124; Clinvar (benign):5 | ||||
| chr14:74019265-74019436 | Common:1; Rare:68 | ||||
| chr14:74493261-74493783 | Common:4; Rare:165; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:74713065-74713200 | Rare:73 |