| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35748912-35749361 | Common:3; Rare:155 | ||||
| chr9:35814976-35815299 | Rare:81 | ||||
| chr9:36190738-36190985 | Common:1; Rare:83 | ||||
| chr9:36191083-36191129 | Rare:15 | ||||
| chr9:36258374-36258625 | Common:2; Rare:61; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:37120181-37120614 | Common:2; Rare:136 | ||||
| chr9:37422538-37422759 | Common:2; Rare:105 | ||||
| chr9:37429588-37429771 | Common:2; Rare:69; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr9:37485787-37486024 | Common:2; Rare:88 | ||||
| chr9:37800689-37800816 | Common:1; Rare:36 | ||||
| chr9:37904067-37904463 | Common:3; Rare:130 | ||||
| chr9:38069203-38069414 | Common:4; Rare:77 | ||||
| chr9:68779960-68780178 | Common:2; Rare:69 | ||||
| chr9:69759913-69760123 | Common:2; Rare:92 | ||||
| chr9:70258824-70259077 | Common:4; Rare:119 |