| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:93452224-93452351 | Rare:25 | ||||
| chr9:93453546-93453701 | Rare:36 | ||||
| chr9:94593786-94593904 | Rare:17 | ||||
| chr9:94639448-94639577 | Common:1; Rare:36; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:94726570-94726732 | Rare:44 | ||||
| chr9:95004124-95004244 | Rare:38 | ||||
| chr9:95317646-95317822 | Common:1; Rare:56; Clinvar:2 | ||||
| chr9:95507378-95507726 | Rare:114 | ||||
| chr9:95516882-95517170 | Common:4; Rare:64 | ||||
| chr9:95875432-95875737 | Common:1; Rare:110 | ||||
| chr9:95875961-95876058 | Common:5; Rare:50; Clinvar (pathogenic):1 | ||||
| chr9:96383584-96383779 | Common:3; Rare:60 | ||||
| chr9:96655284-96655413 | Rare:35 | ||||
| chr9:96778038-96778156 | Rare:37 | ||||
| chr9:97411998-97412183 | Common:3; Rare:47; Clinvar:1; Clinvar (benign):1 |