| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74713058-74713198 | Rare:77 | ||||
| chr14:74763070-74763397 | Rare:94 | ||||
| chr14:74881778-74881973 | Common:1; Rare:91 | ||||
| chr14:75002741-75002972 | Common:1; Rare:72; Clinvar:2 | ||||
| chr14:75063988-75064158 | Common:1; Rare:46 | ||||
| chr14:75069534-75069613 | Rare:16 | ||||
| chr14:75127001-75127110 | Rare:33 | ||||
| chr14:75660797-75660958 | Rare:40 | ||||
| chr14:75661180-75661315 | Common:2; Rare:40 | ||||
| chr14:76151788-76151977 | Rare:64 | ||||
| chr14:76812842-76813051 | Common:2; Rare:73 | ||||
| chr14:77377028-77377398 | Common:3; Rare:102 | ||||
| chr14:77457555-77457876 | Common:1; Rare:94 | ||||
| chr14:77616763-77617105 | Common:1; Rare:75; Clinvar (benign):1 | ||||
| chr14:77708000-77708124 | Rare:60 |