| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133356443-133356630 | Common:1; Rare:87; Clinvar (benign):2 | ||||
| chr9:133375941-133376370 | Common:3; Rare:149 | ||||
| chr9:133417907-133418319 | Common:5; Rare:102 | ||||
| chr9:133459946-133460058 | Common:1; Rare:49 | ||||
| chr9:134135344-134135440 | Common:2; Rare:17 | ||||
| chr9:134641551-134641794 | Common:2; Rare:76 | ||||
| chr9:135499830-135499982 | Common:3; Rare:42 | ||||
| chr9:136410603-136410680 | Rare:40 | ||||
| chr9:136439835-136439899 | Common:1; Rare:27 | ||||
| chr9:136659244-136659479 | Common:2; Rare:54 | ||||
| chr9:136662713-136663022 | Common:2; Rare:73 | ||||
| chr9:136665568-136665815 | Common:2; Rare:65 | ||||
| chr9:136741974-136742102 | Rare:38 | ||||
| chr9:136742908-136743097 | Common:2; Rare:46 | ||||
| chr9:136745846-136746176 | Common:1; Rare:91 |