| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74494031-74494360 | Rare:116; Clinvar (benign):2 | ||||
| chr14:74501436-74501769 | Common:1; Rare:99; Clinvar:3 | ||||
| chr14:74611956-74612017 | Rare:18; Clinvar:4 | ||||
| chr14:74612227-74612549 | Rare:68 | ||||
| chr14:74612560-74612837 | Common:1; Rare:70 | ||||
| chr14:74675870-74676238 | Common:2; Rare:90 | ||||
| chr14:74712996-74713266 | Common:1; Rare:135 | ||||
| chr14:74816956-74817258 | Rare:60 | ||||
| chr14:74834996-74835322 | Rare:65 | ||||
| chr14:74889125-74889358 | Rare:60 | ||||
| chr14:74948510-74948670 | Common:2; Rare:49 | ||||
| chr14:74955372-74955491 | Common:1; Rare:28 | ||||
| chr14:74955557-74955699 | Common:1; Rare:33 | ||||
| chr14:75176376-75176491 | Rare:26 | ||||
| chr14:75176879-75177083 | Rare:46 |