| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:132406774-132406885 | Common:1; Rare:36 | ||||
| chr9:132669930-132670078 | Common:1; Rare:66 | ||||
| chr9:132878262-132878414 | Common:1; Rare:61 | ||||
| chr9:132878860-132878952 | Rare:13 | ||||
| chr9:132944485-132944638 | Rare:51; Clinvar:3; Clinvar (benign):3 | ||||
| chr9:133030447-133030743 | Common:4; Rare:79 | ||||
| chr9:133336117-133336359 | Common:1; Rare:103 | ||||
| chr9:133348009-133348268 | Common:3; Rare:99 | ||||
| chr9:133348809-133349029 | Rare:81 | ||||
| chr9:133356452-133356670 | Common:3; Rare:99; Clinvar (benign):2 | ||||
| chr9:133376003-133376377 | Common:2; Rare:136 | ||||
| chr9:133417874-133418319 | Common:5; Rare:119 | ||||
| chr9:133459946-133460079 | Common:1; Rare:56 | ||||
| chr9:133479066-133479392 | Common:1; Rare:92 | ||||
| chr9:135075214-135075383 | Common:2; Rare:40 |