| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:90331863-90332412 | Common:1; Rare:145 | ||||
| chr14:90396703-90397168 | Common:7; Rare:211 | ||||
| chr14:90397651-90397850 | Common:1; Rare:57 | ||||
| chr14:90397858-90398037 | Common:1; Rare:44 | ||||
| chr14:90398660-90398752 | Common:1; Rare:12 | ||||
| chr14:91060131-91060393 | Common:3; Rare:94 | ||||
| chr14:91060557-91060855 | Common:2; Rare:95 | ||||
| chr14:91113967-91114174 | Common:1; Rare:60 | ||||
| chr14:91114239-91114479 | Rare:49 | ||||
| chr14:91114508-91114772 | Common:2; Rare:39 | ||||
| chr14:91253227-91253582 | Common:3; Rare:90 | ||||
| chr14:91416314-91416569 | Rare:57 | ||||
| chr14:91416847-91416947 | Common:1; Rare:26 | ||||
| chr14:91417539-91417708 | Common:1; Rare:50; Clinvar (benign):1 | ||||
| chr14:91417788-91418327 | Common:4; Rare:152 |