| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:64214130-64214286 | Rare:35; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:64388249-64388424 | Common:2; Rare:86 | ||||
| chr14:64503618-64503887 | Common:2; Rare:102 | ||||
| chr14:64504572-64504832 | Rare:78 | ||||
| chr14:64987086-64987231 | Rare:59 | ||||
| chr14:65411793-65411909 | Common:2; Rare:26 | ||||
| chr14:66507819-66508171 | Rare:140 | ||||
| chr14:66508400-66508530 | Rare:48 | ||||
| chr14:67359744-67360023 | Rare:86 | ||||
| chr14:67360263-67360404 | Common:2; Rare:48 | ||||
| chr14:68979204-68979559 | Common:2; Rare:104 | ||||
| chr14:69259535-69259745 | Common:1; Rare:45 | ||||
| chr14:69398229-69398396 | Rare:72 | ||||
| chr14:69398592-69398723 | Rare:32 | ||||
| chr14:69611456-69611783 | Common:1; Rare:109 |