| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128656656-128657002 | Common:2; Rare:113; Clinvar (pathogenic):1 | ||||
| chr9:128683648-128683905 | Rare:67 | ||||
| chr9:128684951-128685162 | Rare:38 | ||||
| chr9:128724081-128724467 | Common:2; Rare:128 | ||||
| chr9:128772456-128772487 | Rare:2 | ||||
| chr9:128881909-128882213 | Common:2; Rare:103 | ||||
| chr9:128912404-128912801 | Common:2; Rare:65 | ||||
| chr9:128947593-128947735 | Common:1; Rare:64; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:129110653-129110953 | Common:3; Rare:68 | ||||
| chr9:129139910-129140114 | Rare:40 | ||||
| chr9:129753004-129753181 | Rare:47 | ||||
| chr9:129835217-129835481 | Common:2; Rare:107 | ||||
| chr9:130053854-130053933 | Common:1; Rare:24 | ||||
| chr9:130693643-130693827 | Common:1; Rare:71 | ||||
| chr9:131125435-131125637 | Common:1; Rare:94 |