| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:92877983-92878178 | Common:2; Rare:57 | ||||
| chr9:93134228-93134367 | Common:2; Rare:46 | ||||
| chr9:93451455-93451696 | Common:3; Rare:69 | ||||
| chr9:93452294-93452323 | Rare:3 | ||||
| chr9:93452336-93452364 | Rare:6 | ||||
| chr9:93453546-93453687 | Rare:31 | ||||
| chr9:94726568-94726741 | Rare:46 | ||||
| chr9:95317675-95317826 | Common:1; Rare:45; Clinvar:1 | ||||
| chr9:95875441-95875734 | Common:1; Rare:107 | ||||
| chr9:95875972-95876077 | Common:5; Rare:51; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:96383512-96383783 | Common:3; Rare:90 | ||||
| chr9:96655307-96655404 | Rare:22 | ||||
| chr9:97633292-97633872 | Common:6; Rare:182 | ||||
| chr9:97922443-97922600 | Common:3; Rare:81 | ||||
| chr9:97983153-97983607 | Common:2; Rare:170 |