| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:89310931-89311205 | Common:2; Rare:78 | ||||
| chr9:89318401-89318562 | Common:5; Rare:76 | ||||
| chr9:92293648-92293832 | Common:3; Rare:61 | ||||
| chr9:92325329-92325653 | Common:5; Rare:74 | ||||
| chr9:92878003-92878184 | Common:2; Rare:51 | ||||
| chr9:92974223-92974482 | Common:1; Rare:41 | ||||
| chr9:95048380-95048528 | Rare:33 | ||||
| chr9:95516772-95517041 | Common:2; Rare:79; Clinvar (pathogenic):1 | ||||
| chr9:95875459-95875699 | Common:1; Rare:80 | ||||
| chr9:96655307-96655399 | Rare:22 | ||||
| chr9:97039079-97039282 | Rare:80 | ||||
| chr9:97633316-97633821 | Common:6; Rare:156 | ||||
| chr9:98192630-98192850 | Common:5; Rare:61 | ||||
| chr9:98943779-98943922 | Common:3; Rare:44 | ||||
| chr9:99221897-99222355 | Common:2; Rare:181; Clinvar:2; Clinvar (benign):3 |