| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:60052123-60052197 | Rare:12 | ||||
| chr14:60151796-60152060 | Common:2; Rare:58 | ||||
| chr14:60247996-60248641 | Common:3; Rare:147 | ||||
| chr14:60311523-60311712 | Rare:25 | ||||
| chr14:60313200-60313428 | Common:2; Rare:38 | ||||
| chr14:60327589-60327690 | Rare:18 | ||||
| chr14:60327715-60328009 | Common:2; Rare:54 | ||||
| chr14:60331670-60331731 | Common:1; Rare:13 | ||||
| chr14:60485162-60485221 | Rare:12 | ||||
| chr14:60637928-60638094 | Common:1; Rare:38 | ||||
| chr14:60638130-60638213 | Rare:15 | ||||
| chr14:60643725-60644024 | Common:3; Rare:53 | ||||
| chr14:60646462-60646786 | Common:1; Rare:97; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:60648366-60648590 | Rare:66 | ||||
| chr14:60657092-60657252 | Common:1; Rare:45 |