| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74612169-74612435 | Common:1; Rare:47; Clinvar (benign):1 | ||||
| chr14:74713052-74713223 | Rare:95 | ||||
| chr14:74881777-74882016 | Common:1; Rare:106 | ||||
| chr14:75002726-75002972 | Common:1; Rare:78; Clinvar:2 | ||||
| chr14:75063988-75064173 | Common:1; Rare:47 | ||||
| chr14:75126978-75127120 | Rare:53 | ||||
| chr14:75147683-75148043 | Common:3; Rare:57 | ||||
| chr14:75176412-75176971 | Common:1; Rare:144 | ||||
| chr14:75278376-75278742 | Common:1; Rare:83 | ||||
| chr14:75278802-75279185 | Common:2; Rare:114 | ||||
| chr14:75427643-75427727 | Rare:22 | ||||
| chr14:75427913-75428214 | Rare:67 | ||||
| chr14:75578289-75578701 | Common:3; Rare:85; Clinvar (benign):1 | ||||
| chr14:75660819-75661494 | Common:7; Rare:172 | ||||
| chr14:75982979-75983048 | Rare:18 |