| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:136996560-136996663 | Common:1; Rare:31 | ||||
| chr9:137053922-137054229 | Common:2; Rare:107 | ||||
| chr9:137086650-137087209 | Common:3; Rare:225; Clinvar:6; Clinvar (benign):3 | ||||
| chr9:137112253-137112450 | Common:4; Rare:64 | ||||
| chr9:137175882-137176136 | Common:3; Rare:76 | ||||
| chr9:137188552-137188737 | Common:2; Rare:92 | ||||
| chr9:137205646-137205758 | Rare:51 | ||||
| chr9:137231080-137231339 | Rare:63 | ||||
| chr9:137255079-137255442 | Common:7; Rare:136 | ||||
| chr9:137277603-137277735 | Rare:36 | ||||
| chr9:137423127-137423532 | Common:3; Rare:127 | ||||
| chr9:137550193-137550520 | Common:1; Rare:78 | ||||
| chr9:137551632-137551970 | Common:29; Rare:143 | ||||
| chr9:137578864-137579036 | Common:2; Rare:56 | ||||
| chr9:137612288-137612607 | Common:3; Rare:92 |