| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:136796286-136796317 | Rare:10 | ||||
| chr9:136800149-136800427 | Common:5; Rare:87 | ||||
| chr9:136807813-136808206 | Common:3; Rare:140 | ||||
| chr9:136886249-136886540 | Common:2; Rare:85 | ||||
| chr9:136944592-136944870 | Common:1; Rare:112 | ||||
| chr9:136992398-136992476 | Rare:29 | ||||
| chr9:137086652-137087211 | Common:3; Rare:224; Clinvar:6; Clinvar (benign):3 | ||||
| chr9:137112239-137112450 | Common:4; Rare:68 | ||||
| chr9:137114704-137115037 | Common:3; Rare:129 | ||||
| chr9:137188547-137188738 | Common:2; Rare:95 | ||||
| chr9:137188871-137189151 | Common:1; Rare:108 | ||||
| chr9:137205320-137205819 | Common:2; Rare:188 | ||||
| chr9:137423141-137423532 | Common:3; Rare:121 | ||||
| chr9:137550282-137550496 | Rare:32 | ||||
| chr9:137551632-137552209 | Common:29; Rare:213 |