| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133356443-133356607 | Common:1; Rare:75; Clinvar (benign):2 | ||||
| chr9:133375973-133376368 | Common:3; Rare:143 | ||||
| chr9:133417939-133418296 | Common:4; Rare:86 | ||||
| chr9:134641552-134641813 | Common:2; Rare:79; Clinvar (benign):1 | ||||
| chr9:136410603-136410680 | Rare:40 | ||||
| chr9:136746009-136746178 | Common:1; Rare:39 | ||||
| chr9:136944601-136944919 | Common:2; Rare:123 | ||||
| chr9:137188547-137188738 | Common:2; Rare:95 | ||||
| chr9:137205644-137205747 | Rare:44 | ||||
| chr9:137550355-137550496 | Rare:20 | ||||
| chr9:137551653-137551952 | Common:27; Rare:129 | ||||
| chr9:137578864-137579036 | Common:2; Rare:56 | ||||
| chr9:137618797-137619044 | Common:1; Rare:112 | ||||
| chrM:3167-3934 | |||||
| chrM:3956-4332 |