| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:67412049-67412410 | Common:4; Rare:152 | ||||
| chr14:67514819-67514956 | Common:2; Rare:31 | ||||
| chr14:67515010-67515404 | Common:9; Rare:184 | ||||
| chr14:67515600-67516020 | Common:1; Rare:71 | ||||
| chr14:67533002-67533387 | Common:2; Rare:173 | ||||
| chr14:67533702-67534170 | Rare:101 | ||||
| chr14:67600199-67600402 | Common:12; Rare:180; Clinvar (pathogenic):1 | ||||
| chr14:67619563-67619982 | Common:4; Rare:182 | ||||
| chr14:67674106-67674386 | Common:6; Rare:145 | ||||
| chr14:67674524-67675226 | Common:8; Rare:369 | ||||
| chr14:67694720-67695730 | Common:3; Rare:294 | ||||
| chr14:67695663-67695778 | Rare:52 | ||||
| chr14:67816471-67816853 | Common:1; Rare:179; Clinvar:3 | ||||
| chr14:67819601-67819861 | Rare:137 | ||||
| chr14:68791247-68791647 | Common:2; Rare:129 |