| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:94726547-94726732 | Rare:52 | ||||
| chr9:95507405-95507466 | Rare:20 | ||||
| chr9:95875441-95875737 | Common:1; Rare:108 | ||||
| chr9:95875961-95876058 | Common:5; Rare:50; Clinvar (pathogenic):1 | ||||
| chr9:96383584-96383824 | Common:3; Rare:77 | ||||
| chr9:96778048-96778156 | Rare:34 | ||||
| chr9:96854482-96854641 | Common:1; Rare:36 | ||||
| chr9:97412000-97412216 | Common:3; Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:97501517-97501738 | Common:5; Rare:58 | ||||
| chr9:97633261-97633884 | Common:6; Rare:191 | ||||
| chr9:97697202-97697513 | Common:2; Rare:157; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr9:97922434-97922613 | Common:5; Rare:89 | ||||
| chr9:97938056-97938484 | Common:1; Rare:90 | ||||
| chr9:97938487-97938558 | Common:1; Rare:18 | ||||
| chr9:97938567-97938787 | Common:1; Rare:38 |