| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:135075426-135075797 | Common:1; Rare:109 | ||||
| chr9:136327405-136327734 | Common:6; Rare:114 | ||||
| chr9:136410612-136410668 | Rare:27 | ||||
| chr9:136799970-136800035 | Common:3; Rare:20 | ||||
| chr9:136800160-136800403 | Common:4; Rare:71 | ||||
| chr9:136849522-136849868 | Common:1; Rare:119 | ||||
| chr9:136944607-136944909 | Common:2; Rare:112 | ||||
| chr9:136950049-136950232 | Common:1; Rare:77 | ||||
| chr9:136977215-136977680 | Common:1; Rare:99 | ||||
| chr9:137028175-137028454 | Common:1; Rare:85 | ||||
| chr9:137086768-137087146 | Common:2; Rare:154; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:137188538-137188737 | Common:2; Rare:97 | ||||
| chr9:137205646-137205759 | Rare:51 | ||||
| chr9:137618797-137619025 | Common:1; Rare:104 | ||||
| chr9:137666981-137667050 | Rare:17 |