| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128656652-128657002 | Common:2; Rare:115; Clinvar (pathogenic):1 | ||||
| chr9:128724095-128724464 | Common:2; Rare:121 | ||||
| chr9:128881915-128882182 | Common:1; Rare:88 | ||||
| chr9:128921976-128922324 | Common:1; Rare:78 | ||||
| chr9:128947593-128947741 | Common:2; Rare:66; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:129141576-129141663 | Common:2; Rare:26 | ||||
| chr9:129642090-129642422 | Common:3; Rare:85 | ||||
| chr9:129753028-129753203 | Rare:43 | ||||
| chr9:129835210-129835481 | Common:2; Rare:111 | ||||
| chr9:130043079-130043296 | Common:2; Rare:68 | ||||
| chr9:130053847-130053933 | Common:1; Rare:26 | ||||
| chr9:130579447-130579665 | Common:3; Rare:78 | ||||
| chr9:131125425-131125663 | Common:2; Rare:114 | ||||
| chr9:132354938-132355246 | Common:4; Rare:99 | ||||
| chr9:132669898-132670045 | Common:1; Rare:68 |