| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:130172879-130173279 | Common:8; Rare:143 | ||||
| chr9:130578832-130579232 | Common:2; Rare:83 | ||||
| chr9:130579428-130579610 | Common:3; Rare:44 | ||||
| chr9:130693542-130693840 | Common:1; Rare:103 | ||||
| chr9:130834460-130834890 | Common:3; Rare:65 | ||||
| chr9:130834977-130835297 | Common:1; Rare:84 | ||||
| chr9:131096356-131096540 | Common:3; Rare:45 | ||||
| chr9:131125379-131125640 | Common:3; Rare:117 | ||||
| chr9:131289624-131289749 | Rare:29 | ||||
| chr9:131393736-131394139 | Common:1; Rare:153 | ||||
| chr9:131502720-131503200 | Rare:148; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:131531153-131531450 | Common:10; Rare:120 | ||||
| chr9:131739539-131740101 | Common:8; Rare:256 | ||||
| chr9:132079862-132080020 | Rare:34 | ||||
| chr9:132354903-132355221 | Common:4; Rare:107 |