| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34666009-34666282 | Common:2; Rare:66 | ||||
| chr9:35079753-35079821 | Rare:11 | ||||
| chr9:35079917-35080188 | Common:4; Rare:72; Clinvar:3; Clinvar (benign):3 | ||||
| chr9:35103065-35103296 | Common:1; Rare:86 | ||||
| chr9:35657893-35658326 | Common:5; Rare:374; Clinvar:34; Clinvar (benign):13; Clinvar (pathogenic):37 | ||||
| chr9:35665176-35665313 | Common:1; Rare:50 | ||||
| chr9:35673871-35673944 | Common:2; Rare:20 | ||||
| chr9:35685456-35685781 | Common:1; Rare:79; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr9:35689702-35690294 | Common:4; Rare:170; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35732095-35732334 | Common:1; Rare:69 | ||||
| chr9:35732373-35732677 | Common:3; Rare:76 | ||||
| chr9:35748999-35749361 | Common:2; Rare:138 | ||||
| chr9:36190747-36190988 | Common:1; Rare:79 | ||||
| chr9:36258386-36258622 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:36572772-36572975 | Common:1; Rare:56 |