| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49767423-49767452 | Rare:4 | ||||
| chr14:49767585-49767770 | Common:2; Rare:54 | ||||
| chr14:49767940-49768245 | Common:2; Rare:112 | ||||
| chr14:49852558-49853109 | Common:4; Rare:157 | ||||
| chr14:49892774-49893227 | Common:1; Rare:177 | ||||
| chr14:49893427-49893580 | Common:2; Rare:50 | ||||
| chr14:50116479-50116773 | Common:1; Rare:145 | ||||
| chr14:50231054-50231251 | Common:2; Rare:68; Clinvar (benign):1 | ||||
| chr14:50231552-50231806 | Rare:74 | ||||
| chr14:50231847-50232054 | Common:1; Rare:83 | ||||
| chr14:50311911-50311998 | Rare:30 | ||||
| chr14:50312094-50312456 | Common:2; Rare:149; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:50312526-50312772 | Common:7; Rare:83 | ||||
| chr14:50363789-50364102 | Rare:75 | ||||
| chr14:50531970-50532271 | Common:2; Rare:77 |