| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:37485737-37486056 | Common:3; Rare:117 | ||||
| chr9:37592471-37592648 | Common:2; Rare:66 | ||||
| chr9:37784899-37785149 | Common:1; Rare:114; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr9:37800522-37800624 | Common:2; Rare:25 | ||||
| chr9:37800707-37800830 | Rare:38 | ||||
| chr9:37801405-37801673 | Common:2; Rare:67 | ||||
| chr9:37903701-37903756 | Rare:15 | ||||
| chr9:37904057-37904229 | Rare:56 | ||||
| chr9:37904340-37904442 | Rare:38 | ||||
| chr9:68356346-68356635 | Common:8; Rare:51 | ||||
| chr9:68356852-68357130 | Common:5; Rare:74 | ||||
| chr9:68779843-68780173 | Common:4; Rare:116 | ||||
| chr9:69120767-69121206 | Common:3; Rare:86 | ||||
| chr9:69121353-69121517 | Common:1; Rare:41 | ||||
| chr9:69759930-69760094 | Common:2; Rare:80 |