| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:135502251-135502395 | Common:2; Rare:30 | ||||
| chr9:136118825-136119045 | Common:3; Rare:96 | ||||
| chr9:136327224-136327623 | Common:5; Rare:135 | ||||
| chr9:136410345-136410749 | Common:7; Rare:173; Clinvar (pathogenic):1 | ||||
| chr9:136411927-136412049 | Common:1; Rare:38 | ||||
| chr9:136439770-136440161 | Common:1; Rare:125 | ||||
| chr9:136448245-136448416 | Common:3; Rare:56 | ||||
| chr9:136483765-136483883 | Rare:35 | ||||
| chr9:136546046-136546231 | Rare:79 | ||||
| chr9:136807758-136808116 | Common:2; Rare:140 | ||||
| chr9:136808214-136808314 | Rare:30 | ||||
| chr9:136849292-136849868 | Common:3; Rare:231 | ||||
| chr9:136866195-136866374 | Common:1; Rare:76 | ||||
| chr9:136886249-136886533 | Common:2; Rare:83 | ||||
| chr9:136944598-136944947 | Common:2; Rare:133 |