| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:92039774-92039814 | Rare:7; Clinvar:1 | ||||
| chr14:92039831-92039926 | Rare:18 | ||||
| chr14:92039932-92040472 | Common:5; Rare:127; Clinvar:6; Clinvar (benign):2 | ||||
| chr14:92040838-92040951 | Rare:21 | ||||
| chr14:92106218-92106386 | Common:1; Rare:58 | ||||
| chr14:92106514-92106869 | Common:3; Rare:99 | ||||
| chr14:92121076-92121372 | Common:5; Rare:58 | ||||
| chr14:92121606-92121761 | Common:1; Rare:70 | ||||
| chr14:92121892-92122188 | Rare:83 | ||||
| chr14:92122353-92122520 | Common:1; Rare:47 | ||||
| chr14:92513052-92513405 | Common:3; Rare:81 | ||||
| chr14:92513411-92513460 | Rare:15 | ||||
| chr14:92513475-92513583 | Rare:24 | ||||
| chr14:92513615-92513711 | Common:2; Rare:26 | ||||
| chr14:92513742-92513868 | Common:1; Rare:24 |