| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128947549-128947719 | Common:1; Rare:79; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:129110583-129110953 | Common:3; Rare:83 | ||||
| chr9:129139935-129140129 | Rare:40 | ||||
| chr9:129141905-129142041 | Common:3; Rare:28 | ||||
| chr9:129834711-129834863 | Common:2; Rare:51 | ||||
| chr9:129835112-129835509 | Common:4; Rare:151 | ||||
| chr9:130053622-130053741 | Rare:23 | ||||
| chr9:130053846-130054035 | Common:1; Rare:71 | ||||
| chr9:130579410-130579754 | Common:7; Rare:129 | ||||
| chr9:130693544-130693800 | Rare:78 | ||||
| chr9:130835095-130835373 | Common:8; Rare:74 | ||||
| chr9:131125425-131125651 | Common:2; Rare:108 | ||||
| chr9:131484754-131485007 | Common:1; Rare:68 | ||||
| chr9:131502860-131503210 | Rare:105; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:132354932-132355248 | Common:4; Rare:104 |