| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:97501506-97501738 | Common:6; Rare:62 | ||||
| chr9:97633271-97633395 | Rare:32 | ||||
| chr9:97633521-97633860 | Common:4; Rare:109 | ||||
| chr9:97922179-97922367 | Common:2; Rare:64 | ||||
| chr9:97922471-97922580 | Common:3; Rare:55 | ||||
| chr9:97983209-97983572 | Common:2; Rare:140 | ||||
| chr9:98056565-98056772 | Common:1; Rare:69 | ||||
| chr9:99221916-99222365 | Common:2; Rare:178; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:99821633-99821893 | Rare:90 | ||||
| chr9:99906574-99906717 | Rare:67 | ||||
| chr9:100098930-100099323 | Common:3; Rare:111; Clinvar:2 | ||||
| chr9:100352831-100353103 | Rare:100 | ||||
| chr9:101028628-101028945 | Common:4; Rare:101 | ||||
| chr9:101398565-101398910 | Common:1; Rare:118 | ||||
| chr9:101487000-101487195 | Common:2; Rare:51 |