| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:92482498-92482821 | Rare:44 | ||||
| chr9:92670017-92670314 | Common:1; Rare:90 | ||||
| chr9:93134227-93134367 | Common:2; Rare:46 | ||||
| chr9:93451435-93451702 | Common:3; Rare:71 | ||||
| chr9:93452297-93452387 | Rare:15 | ||||
| chr9:93453546-93453687 | Rare:31 | ||||
| chr9:94726551-94726732 | Rare:51 | ||||
| chr9:95018432-95018490 | Rare:11 | ||||
| chr9:95048387-95048644 | Rare:63 | ||||
| chr9:95505876-95506188 | Common:1; Rare:106 | ||||
| chr9:95506560-95506652 | Rare:38; Clinvar:5; Clinvar (benign):6 | ||||
| chr9:95507357-95507714 | Rare:113 | ||||
| chr9:95875429-95875703 | Common:1; Rare:93 | ||||
| chr9:95875961-95876068 | Common:5; Rare:55; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:96655303-96655424 | Rare:30 |