| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:68817613-68817699 | Common:1; Rare:34 | ||||
| chr15:68820741-68821046 | Rare:93 | ||||
| chr15:68930381-68930542 | Common:1; Rare:52 | ||||
| chr15:69414186-69414366 | Rare:49 | ||||
| chr15:69452694-69452848 | Common:3; Rare:70 | ||||
| chr15:70892398-70892880 | Common:1; Rare:116 | ||||
| chr15:72118168-72118425 | Common:2; Rare:80 | ||||
| chr15:72231101-72231472 | Common:3; Rare:116 | ||||
| chr15:72375951-72376043 | Common:2; Rare:45; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr15:72474210-72474294 | Rare:29 | ||||
| chr15:72686149-72686220 | Common:2; Rare:28; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:73994595-73994756 | Rare:32 | ||||
| chr15:74128209-74128305 | Rare:21 | ||||
| chr15:74129526-74129689 | Rare:26 | ||||
| chr15:74130130-74130392 | Rare:55 |