| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128552408-128552622 | Rare:86; Clinvar:1 | ||||
| chr9:128656635-128656816 | Common:2; Rare:83; Clinvar (pathogenic):1 | ||||
| chr9:128724095-128724467 | Common:2; Rare:123 | ||||
| chr9:128921982-128922326 | Common:1; Rare:79 | ||||
| chr9:128947598-128947729 | Common:1; Rare:59; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:129110655-129110953 | Common:3; Rare:68 | ||||
| chr9:129139954-129140129 | Rare:35 | ||||
| chr9:129626004-129626231 | Common:3; Rare:62 | ||||
| chr9:129835210-129835486 | Common:2; Rare:113 | ||||
| chr9:130043086-130043336 | Common:2; Rare:85 | ||||
| chr9:130053847-130053979 | Common:1; Rare:54 | ||||
| chr9:130579428-130579677 | Common:7; Rare:98 | ||||
| chr9:130693602-130693794 | Rare:63 | ||||
| chr9:131125342-131125649 | Common:3; Rare:133 | ||||
| chr9:131502866-131503024 | Rare:55; Clinvar:3 |