| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133376003-133376388 | Common:2; Rare:141 | ||||
| chr9:133417917-133418288 | Common:4; Rare:94 | ||||
| chr9:134135282-134135382 | Common:1; Rare:18 | ||||
| chr9:136118812-136118900 | Common:3; Rare:40 | ||||
| chr9:136410591-136410697 | Common:1; Rare:61 | ||||
| chr9:136662764-136662921 | Common:1; Rare:42 | ||||
| chr9:136687192-136687653 | Common:3; Rare:154; Clinvar:6; Clinvar (benign):2 | ||||
| chr9:136800183-136800483 | Common:4; Rare:84 | ||||
| chr9:136807813-136808138 | Common:3; Rare:118 | ||||
| chr9:136835664-136835792 | Common:1; Rare:33 | ||||
| chr9:136849567-136849812 | Common:1; Rare:90 | ||||
| chr9:136852042-136852378 | Rare:100 | ||||
| chr9:136886249-136886533 | Common:2; Rare:83 | ||||
| chr9:136944592-136944947 | Common:2; Rare:135 | ||||
| chr9:136949471-136949644 | Rare:38 |