| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:20684074-20684291 | Common:3; Rare:86 | ||||
| chr9:21802483-21802677 | Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:23826145-23826417 | Common:2; Rare:107 | ||||
| chr9:26892738-26892847 | Rare:60 | ||||
| chr9:26947128-26947249 | Rare:45 | ||||
| chr9:26956265-26956470 | Common:2; Rare:77 | ||||
| chr9:27529709-27529856 | Common:4; Rare:44 | ||||
| chr9:27573430-27573524 | Common:5; Rare:50 | ||||
| chr9:27573709-27573972 | Common:2; Rare:85; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:32384544-32384729 | Common:1; Rare:75 | ||||
| chr9:32526173-32526374 | Common:3; Rare:62 | ||||
| chr9:32552557-32552653 | Common:1; Rare:18; Clinvar:2 | ||||
| chr9:32573041-32573218 | Common:2; Rare:66 | ||||
| chr9:33001538-33001751 | Common:3; Rare:106; Clinvar (benign):4 | ||||
| chr9:33025056-33025383 | Common:7; Rare:134 |