| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50116524-50116696 | Rare:92 | ||||
| chr14:50312198-50312329 | Rare:45 | ||||
| chr14:50396821-50396987 | Common:2; Rare:48 | ||||
| chr14:50532526-50532787 | Common:3; Rare:88 | ||||
| chr14:50668287-50668556 | Common:3; Rare:97 | ||||
| chr14:50944323-50944567 | Common:4; Rare:95; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:51240132-51240413 | Rare:120 | ||||
| chr14:51651662-51651968 | Common:4; Rare:84 | ||||
| chr14:52003940-52004233 | Common:2; Rare:95 | ||||
| chr14:52069057-52069224 | Common:2; Rare:31 | ||||
| chr14:52314112-52314333 | Common:1; Rare:61 | ||||
| chr14:52695477-52695812 | Common:1; Rare:93 | ||||
| chr14:52707100-52707300 | Common:1; Rare:78 | ||||
| chr14:52791576-52791873 | Common:2; Rare:102 | ||||
| chr14:55027046-55027301 | Common:2; Rare:72 |