| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:89956332-89956752 | Common:5; Rare:99; Clinvar:1; Clinvar (benign):4 | ||||
| chr14:90256450-90256671 | Common:3; Rare:69 | ||||
| chr14:90256958-90257092 | Rare:25 | ||||
| chr14:90331580-90331745 | Common:1; Rare:41 | ||||
| chr14:90331857-90332418 | Common:1; Rare:147 | ||||
| chr14:90396774-90397173 | Common:7; Rare:197 | ||||
| chr14:90397644-90397763 | Rare:31 | ||||
| chr14:90397776-90397988 | Common:1; Rare:58 | ||||
| chr14:90397996-90398236 | Common:5; Rare:55 | ||||
| chr14:90398675-90398773 | Common:1; Rare:16 | ||||
| chr14:90816164-90816215 | Rare:13 | ||||
| chr14:90816226-90816264 | Rare:5 | ||||
| chr14:90816266-90816531 | Rare:55 | ||||
| chr14:91059992-91060087 | Common:1; Rare:24 | ||||
| chr14:91060262-91060414 | Common:2; Rare:66 |