| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:95317670-95317828 | Common:1; Rare:47; Clinvar:2 | ||||
| chr9:95516765-95517051 | Common:2; Rare:83; Clinvar (pathogenic):1 | ||||
| chr9:95875547-95875703 | Common:1; Rare:53 | ||||
| chr9:95875961-95876037 | Common:4; Rare:37 | ||||
| chr9:97039076-97039342 | Common:1; Rare:102 | ||||
| chr9:97633261-97633458 | Common:1; Rare:52 | ||||
| chr9:97633535-97633848 | Common:4; Rare:97 | ||||
| chr9:97697294-97697482 | Common:2; Rare:98; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:98943238-98943583 | Common:1; Rare:63 | ||||
| chr9:99221922-99222359 | Common:2; Rare:166; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:99821693-99822001 | Rare:87 | ||||
| chr9:99906570-99906713 | Rare:67 | ||||
| chr9:100098964-100099323 | Common:3; Rare:103; Clinvar:2 | ||||
| chr9:100352860-100353096 | Rare:86 | ||||
| chr9:101028611-101028795 | Common:2; Rare:61 |