| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:125200428-125200590 | Common:1; Rare:60 | ||||
| chr9:125261638-125261841 | Common:2; Rare:74 | ||||
| chr9:126804919-126805035 | Rare:36 | ||||
| chr9:127245190-127245341 | Common:1; Rare:37 | ||||
| chr9:127424294-127424406 | Rare:36 | ||||
| chr9:127451272-127451547 | Common:3; Rare:116; Clinvar (benign):1 | ||||
| chr9:127937824-127937873 | Common:1; Rare:19; Clinvar (benign):1 | ||||
| chr9:128160139-128160446 | Common:2; Rare:83 | ||||
| chr9:128191811-128191867 | Rare:11 | ||||
| chr9:128275936-128276327 | Common:5; Rare:185 | ||||
| chr9:128322410-128322485 | Rare:30 | ||||
| chr9:128322751-128322866 | Common:2; Rare:46; Clinvar (benign):5 | ||||
| chr9:128371223-128371379 | Rare:50 | ||||
| chr9:128504635-128504747 | Rare:43; Clinvar:3 | ||||
| chr9:128552309-128552611 | Common:1; Rare:107; Clinvar:1 |