| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133418033-133418319 | Common:4; Rare:59 | ||||
| chr9:134135365-134135424 | Common:1; Rare:10 | ||||
| chr9:134641551-134641812 | Common:2; Rare:80; Clinvar (benign):1 | ||||
| chr9:135545974-135546161 | Common:1; Rare:46 | ||||
| chr9:135961137-135961394 | Common:5; Rare:108 | ||||
| chr9:136410609-136410667 | Rare:29 | ||||
| chr9:136745847-136745978 | Rare:47 | ||||
| chr9:136746010-136746170 | Common:1; Rare:38 | ||||
| chr9:136800121-136800399 | Common:5; Rare:86 | ||||
| chr9:136849596-136849765 | Common:1; Rare:66 | ||||
| chr9:136886249-136886533 | Common:2; Rare:83 | ||||
| chr9:137086811-137087081 | Rare:109; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:137188545-137188723 | Common:2; Rare:91 | ||||
| chr9:137205407-137205723 | Common:1; Rare:110 | ||||
| chr9:137550355-137550480 | Rare:19 |