| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:23821680-23821970 | Common:3; Rare:148 | ||||
| chr9:23826205-23826551 | Common:1; Rare:140 | ||||
| chr9:26892338-26892485 | Rare:65 | ||||
| chr9:26892734-26892895 | Common:1; Rare:79 | ||||
| chr9:26947089-26947289 | Common:1; Rare:76 | ||||
| chr9:26956255-26956470 | Common:2; Rare:80 | ||||
| chr9:27573422-27573529 | Common:5; Rare:55 | ||||
| chr9:27573728-27573972 | Common:2; Rare:77; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:32552557-32552655 | Common:1; Rare:18; Clinvar:2 | ||||
| chr9:32573047-32573218 | Common:2; Rare:64 | ||||
| chr9:33001529-33001804 | Common:3; Rare:129; Clinvar (benign):4 | ||||
| chr9:33025018-33025407 | Common:7; Rare:151 | ||||
| chr9:33076583-33076823 | Common:2; Rare:76 | ||||
| chr9:33264510-33264884 | Common:2; Rare:113 | ||||
| chr9:33290343-33290570 | Common:2; Rare:85 |