| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34048870-34048992 | Common:1; Rare:49 | ||||
| chr9:34049178-34049268 | Common:1; Rare:21 | ||||
| chr9:34178937-34179078 | Common:1; Rare:39 | ||||
| chr9:34329181-34329612 | Common:1; Rare:135 | ||||
| chr9:34662654-34662872 | Rare:48 | ||||
| chr9:34665353-34665665 | Rare:98 | ||||
| chr9:34691257-34691350 | Rare:9 | ||||
| chr9:35079908-35080107 | Common:5; Rare:49; Clinvar:3; Clinvar (benign):4 | ||||
| chr9:35646823-35646951 | Rare:26 | ||||
| chr9:35657841-35658436 | Common:11; Rare:470; Clinvar:42; Clinvar (benign):16; Clinvar (pathogenic):40 | ||||
| chr9:35685405-35685796 | Common:1; Rare:95; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr9:35689702-35690099 | Common:3; Rare:126; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35691081-35691255 | Common:1; Rare:38 | ||||
| chr9:35706532-35706789 | Rare:63 | ||||
| chr9:35732089-35732334 | Common:1; Rare:70 |