| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:129394418-129394590 | Rare:33 | ||||
| chr9:129413675-129414016 | Common:3; Rare:147 | ||||
| chr9:129460289-129460612 | Common:3; Rare:65 | ||||
| chr9:129495980-129496230 | Common:2; Rare:78 | ||||
| chr9:130254480-130254647 | Common:2; Rare:43 | ||||
| chr9:131373410-131373725 | Common:1; Rare:76 | ||||
| chr9:132003112-132003292 | Rare:18 | ||||
| chr9:132546236-132546361 | Common:1; Rare:37 | ||||
| chr9:133119601-133119842 | Common:3; Rare:56 | ||||
| chr9:133120317-133120497 | Common:5; Rare:43 | ||||
| chr9:133133320-133133539 | Rare:42 | ||||
| chr9:133627054-133627200 | Rare:29 | ||||
| chr9:133634255-133634508 | Common:4; Rare:60 | ||||
| chr9:133635227-133635394 | Common:3; Rare:35; Clinvar (benign):1 | ||||
| chr9:133705767-133705905 | Common:1; Rare:24 |