| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:67521639-67521755 | Rare:28 | ||||
| chr15:69160342-69160651 | Common:4; Rare:94 | ||||
| chr15:69414211-69414366 | Rare:44 | ||||
| chr15:70763409-70763711 | Common:2; Rare:99 | ||||
| chr15:72118168-72118420 | Common:2; Rare:77 | ||||
| chr15:72231160-72231516 | Common:3; Rare:113 | ||||
| chr15:72375941-72376129 | Common:2; Rare:78; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr15:72686067-72686220 | Common:2; Rare:56; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:73633215-73633559 | Common:1; Rare:132 | ||||
| chr15:74461115-74461298 | Rare:59 | ||||
| chr15:74938018-74938265 | Common:2; Rare:88 | ||||
| chr15:75335946-75336084 | Common:1; Rare:64 | ||||
| chr15:75368585-75368750 | Rare:45 | ||||
| chr15:75640166-75640441 | Common:2; Rare:94 | ||||
| chr15:77420127-77420494 | Common:2; Rare:115 |