| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:129892040-129892269 | Common:1; Rare:44 | ||||
| chr9:129892881-129892987 | Rare:19 | ||||
| chr9:130601437-130601554 | Rare:19 | ||||
| chr9:130633600-130633706 | Common:1; Rare:27 | ||||
| chr9:130712969-130713078 | Rare:34 | ||||
| chr9:130836862-130837142 | Common:3; Rare:47 | ||||
| chr9:130839019-130839059 | Rare:5 | ||||
| chr9:130857844-130857952 | Common:1; Rare:31 | ||||
| chr9:130860892-130861154 | Common:1; Rare:54 | ||||
| chr9:131507253-131507432 | Common:1; Rare:53; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:132282372-132282584 | Common:2; Rare:46 | ||||
| chr9:133352568-133352696 | Common:1; Rare:64; Clinvar (benign):2 | ||||
| chr9:133374742-133374764 | Rare:6 | ||||
| chr9:133711396-133711505 | Common:1; Rare:20 | ||||
| chr9:134141140-134141348 | Common:2; Rare:43 |