| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49852713-49853149 | Common:3; Rare:121 | ||||
| chr14:49892909-49893136 | Rare:94 | ||||
| chr14:50312140-50312376 | Rare:107; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:50396819-50396995 | Common:2; Rare:50 | ||||
| chr14:50532317-50532621 | Common:4; Rare:79 | ||||
| chr14:50561078-50561186 | Rare:21 | ||||
| chr14:50668287-50668556 | Common:3; Rare:97 | ||||
| chr14:50944310-50944590 | Common:4; Rare:103; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:51095071-51095390 | Common:4; Rare:134 | ||||
| chr14:51240107-51240397 | Common:1; Rare:124 | ||||
| chr14:51651432-51651471 | Rare:18 | ||||
| chr14:51651719-51651984 | Common:4; Rare:78 | ||||
| chr14:51989388-51989700 | Common:2; Rare:105 | ||||
| chr14:51999625-51999796 | Common:1; Rare:36 | ||||
| chr14:52003958-52004227 | Common:2; Rare:88 |