| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:32526155-32526348 | Common:4; Rare:61 | ||||
| chr9:33001529-33001775 | Common:3; Rare:120; Clinvar (benign):4 | ||||
| chr9:33025066-33025432 | Common:8; Rare:146 | ||||
| chr9:33076604-33076850 | Common:2; Rare:83 | ||||
| chr9:33166767-33166966 | Rare:65; Clinvar:3 | ||||
| chr9:33167093-33167514 | Common:1; Rare:146; Clinvar:6 | ||||
| chr9:33264551-33265129 | Common:1; Rare:174 | ||||
| chr9:33290367-33290591 | Common:2; Rare:88 | ||||
| chr9:33473841-33474169 | Common:4; Rare:101 | ||||
| chr9:34048851-34048992 | Common:2; Rare:60 | ||||
| chr9:34049164-34049268 | Common:1; Rare:29 | ||||
| chr9:34049356-34049581 | Common:1; Rare:71 | ||||
| chr9:34126361-34126476 | Rare:49 | ||||
| chr9:34178935-34179133 | Common:1; Rare:54 | ||||
| chr9:34179275-34179450 | Rare:32 |