| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49586341-49586776 | Common:1; Rare:233 | ||||
| chr14:49598731-49599005 | Common:1; Rare:99 | ||||
| chr14:49620561-49620837 | Common:2; Rare:114; Clinvar:3 | ||||
| chr14:49778173-49778488 | Common:1; Rare:65 | ||||
| chr14:49795845-49796180 | Rare:60 | ||||
| chr14:49892898-49893154 | Rare:109 | ||||
| chr14:50312146-50312396 | Common:1; Rare:110 | ||||
| chr14:50396874-50396986 | Common:1; Rare:29 | ||||
| chr14:50532509-50532805 | Common:3; Rare:92 | ||||
| chr14:50561120-50561341 | Common:1; Rare:35 | ||||
| chr14:50668340-50668558 | Common:4; Rare:85 | ||||
| chr14:50944380-50944546 | Common:3; Rare:66; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:51095095-51095298 | Common:4; Rare:81 | ||||
| chr14:51240021-51240364 | Common:2; Rare:129 | ||||
| chr14:51651611-51651996 | Common:4; Rare:106 |