| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:26947102-26947249 | Common:1; Rare:56 | ||||
| chr9:26947252-26947299 | Rare:14 | ||||
| chr9:26947403-26947557 | Common:1; Rare:54 | ||||
| chr9:26956302-26956459 | Common:2; Rare:57 | ||||
| chr9:27529738-27529899 | Common:4; Rare:53 | ||||
| chr9:27573422-27573535 | Common:5; Rare:61 | ||||
| chr9:27573709-27573972 | Common:2; Rare:85; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:32384512-32384732 | Common:1; Rare:83 | ||||
| chr9:32573064-32573204 | Common:2; Rare:53 | ||||
| chr9:33025092-33025383 | Common:7; Rare:120 | ||||
| chr9:33076587-33076855 | Common:2; Rare:84 | ||||
| chr9:33166843-33166975 | Rare:47 | ||||
| chr9:33167150-33167490 | Common:1; Rare:117; Clinvar:5 | ||||
| chr9:33264944-33265147 | Rare:64 | ||||
| chr9:33290350-33290575 | Common:2; Rare:84 |