| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:38424451-38424622 | Rare:47 | ||||
| chr9:38620512-38620773 | Rare:70 | ||||
| chr9:65675725-65675964 | Rare:58 | ||||
| chr9:66900540-66900850 | Common:3; Rare:99 | ||||
| chr9:68705115-68705286 | Common:1; Rare:48 | ||||
| chr9:68705421-68705708 | Common:2; Rare:82 | ||||
| chr9:68779899-68780112 | Common:3; Rare:80 | ||||
| chr9:69035870-69036240 | Common:3; Rare:137; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:69174021-69174304 | Common:4; Rare:83 | ||||
| chr9:69672240-69672560 | Common:2; Rare:87 | ||||
| chr9:69759390-69759690 | Common:2; Rare:85 | ||||
| chr9:69759888-69760210 | Common:3; Rare:127 | ||||
| chr9:70043500-70043860 | Common:1; Rare:57 | ||||
| chr9:70258807-70259076 | Common:4; Rare:126 | ||||
| chr9:70414309-70414502 | Rare:44 |