| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:134135960-134136196 | Common:8; Rare:161 | ||||
| chr9:134326010-134326549 | Common:5; Rare:319 | ||||
| chr9:134371692-134372100 | Rare:176 | ||||
| chr9:134641547-134641905 | Common:4; Rare:192; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:135075214-135075546 | Common:2; Rare:78 | ||||
| chr9:135087418-135087691 | Common:1; Rare:59 | ||||
| chr9:135478763-135479137 | Common:3; Rare:132 | ||||
| chr9:135479630-135480015 | Common:4; Rare:212 | ||||
| chr9:135500340-135500710 | Common:8; Rare:150 | ||||
| chr9:135907483-135907935 | Common:6; Rare:310 | ||||
| chr9:135961127-135961584 | Common:15; Rare:305 | ||||
| chr9:136095228-136095391 | Rare:97 | ||||
| chr9:136118715-136119134 | Common:9; Rare:300 | ||||
| chr9:136245520-136245740 | Common:4; Rare:133 | ||||
| chr9:136245766-136246084 | Common:4; Rare:76 |