| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:66900571-66900804 | Common:3; Rare:74 | ||||
| chr9:68356354-68356777 | Common:8; Rare:90 | ||||
| chr9:68356968-68357143 | Common:3; Rare:54 | ||||
| chr9:68779845-68780172 | Common:3; Rare:116 | ||||
| chr9:69035937-69036082 | Common:3; Rare:68; Clinvar (benign):1 | ||||
| chr9:69672277-69672579 | Common:1; Rare:89 | ||||
| chr9:69759916-69760099 | Common:2; Rare:86 | ||||
| chr9:70258823-70259081 | Common:4; Rare:120 | ||||
| chr9:70414136-70414211 | Rare:20 | ||||
| chr9:70414303-70414523 | Rare:49 | ||||
| chr9:70869047-70869136 | Rare:19 | ||||
| chr9:71768828-71769046 | Common:2; Rare:65 | ||||
| chr9:71911184-71911499 | Common:2; Rare:90 | ||||
| chr9:72365188-72365420 | Common:2; Rare:85 | ||||
| chr9:72577234-72577366 | Rare:16 |