| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:26947146-26947216 | Rare:26 | ||||
| chr9:26956255-26956446 | Common:2; Rare:73 | ||||
| chr9:32573078-32573218 | Common:2; Rare:53 | ||||
| chr9:33025092-33025383 | Common:7; Rare:120 | ||||
| chr9:33290363-33290561 | Common:2; Rare:74 | ||||
| chr9:34049197-34049293 | Common:1; Rare:26 | ||||
| chr9:34126665-34126852 | Common:1; Rare:54 | ||||
| chr9:34178937-34179058 | Common:1; Rare:33 | ||||
| chr9:34329187-34329614 | Common:1; Rare:135 | ||||
| chr9:35657950-35658318 | Common:5; Rare:296; Clinvar:24; Clinvar (benign):12; Clinvar (pathogenic):35 | ||||
| chr9:35689702-35689988 | Common:3; Rare:92; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35732073-35732683 | Common:5; Rare:168 | ||||
| chr9:35749019-35749325 | Common:1; Rare:113 | ||||
| chr9:35814983-35815299 | Rare:81 | ||||
| chr9:37592498-37592634 | Common:2; Rare:58 |