| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:67360205-67360430 | Common:3; Rare:72 | ||||
| chr14:67412051-67412412 | Common:2; Rare:85 | ||||
| chr14:67532981-67533401 | Common:1; Rare:95 | ||||
| chr14:67533417-67533572 | Common:3; Rare:43 | ||||
| chr14:67599978-67600151 | Common:3; Rare:53 | ||||
| chr14:67600178-67600486 | Common:7; Rare:98; Clinvar (pathogenic):1 | ||||
| chr14:67619535-67619978 | Common:2; Rare:115 | ||||
| chr14:67674206-67674364 | Common:2; Rare:44 | ||||
| chr14:67674524-67674733 | Common:1; Rare:55 | ||||
| chr14:67674781-67675217 | Common:3; Rare:99 | ||||
| chr14:67695501-67695853 | Common:1; Rare:122 | ||||
| chr14:67816516-67816838 | Common:1; Rare:65; Clinvar:1 | ||||
| chr14:67819653-67819857 | Rare:51 | ||||
| chr14:68791011-68791303 | Common:1; Rare:78 | ||||
| chr14:68792879-68793273 | Common:1; Rare:127 |