| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:91060165-91060393 | Common:4; Rare:151 | ||||
| chr14:91060553-91060694 | Rare:50 | ||||
| chr14:91417754-91418320 | Common:6; Rare:274 | ||||
| chr14:91510227-91510915 | Common:4; Rare:346 | ||||
| chr14:91836415-91836724 | Common:24; Rare:105 | ||||
| chr14:91947638-91947779 | Common:2; Rare:49; Clinvar:2; Clinvar (benign):4 | ||||
| chr14:92039354-92039629 | Common:2; Rare:80; Clinvar (benign):2 | ||||
| chr14:92040013-92040198 | Common:5; Rare:98; Clinvar:3; Clinvar (benign):3 | ||||
| chr14:92040270-92040530 | Common:2; Rare:74 | ||||
| chr14:92106550-92106822 | Common:6; Rare:165 | ||||
| chr14:92121628-92122110 | Common:10; Rare:279 | ||||
| chr14:92748518-92748817 | Rare:140 | ||||
| chr14:92793980-92794459 | Rare:266 | ||||
| chr14:93115189-93115487 | Common:4; Rare:223 | ||||
| chr14:93115802-93116012 | Common:2; Rare:125 |