| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33001560-33001789 | Common:3; Rare:105; Clinvar (benign):3 | ||||
| chr9:33025090-33025304 | Common:6; Rare:91 | ||||
| chr9:33076604-33076818 | Common:2; Rare:73 | ||||
| chr9:33264590-33264888 | Common:1; Rare:83 | ||||
| chr9:33290255-33290564 | Common:3; Rare:104 | ||||
| chr9:34126375-34126471 | Rare:39 | ||||
| chr9:34126627-34126786 | Rare:52 | ||||
| chr9:34178952-34179070 | Common:1; Rare:33 | ||||
| chr9:34329172-34329598 | Rare:132 | ||||
| chr9:34646539-34646684 | Common:1; Rare:36; Clinvar:2 | ||||
| chr9:35103065-35103279 | Common:1; Rare:80 | ||||
| chr9:35657853-35658322 | Common:7; Rare:409; Clinvar:42; Clinvar (benign):15; Clinvar (pathogenic):40 | ||||
| chr9:35673834-35673928 | Common:2; Rare:23 | ||||
| chr9:35732373-35732631 | Common:2; Rare:63 | ||||
| chr9:35749007-35749369 | Common:2; Rare:137 |