| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128552408-128552611 | Rare:79; Clinvar:1 | ||||
| chr9:128724114-128724214 | Common:1; Rare:32 | ||||
| chr9:128947604-128947716 | Common:1; Rare:51; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:129835217-129835475 | Common:2; Rare:104 | ||||
| chr9:130043119-130043336 | Common:2; Rare:79 | ||||
| chr9:130053854-130053929 | Common:1; Rare:24 | ||||
| chr9:131502850-131502996 | Rare:58; Clinvar:3 | ||||
| chr9:131531188-131531332 | Common:9; Rare:66 | ||||
| chr9:132878279-132878357 | Common:1; Rare:26 | ||||
| chr9:133348043-133348246 | Common:2; Rare:76 | ||||
| chr9:133356470-133356589 | Common:1; Rare:49; Clinvar (benign):2 | ||||
| chr9:133376024-133376332 | Common:1; Rare:112 | ||||
| chr9:134641547-134641858 | Common:2; Rare:95; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:136662764-136662921 | Common:1; Rare:42 | ||||
| chr9:136977362-136977549 | Rare:42 |