| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128945582-128945859 | Rare:76; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr9:129177221-129177477 | Common:2; Rare:95 | ||||
| chr9:129208535-129208626 | Rare:21 | ||||
| chr9:129208826-129208950 | Common:2; Rare:25 | ||||
| chr9:129333836-129333971 | Rare:22 | ||||
| chr9:129828218-129828394 | Common:1; Rare:55 | ||||
| chr9:129829288-129829450 | Rare:52 | ||||
| chr9:130690073-130690312 | Common:1; Rare:44 | ||||
| chr9:131373392-131373679 | Common:1; Rare:64 | ||||
| chr9:131395426-131395597 | Rare:42 | ||||
| chr9:131488506-131488635 | Rare:33 | ||||
| chr9:131554080-131554383 | Common:4; Rare:55 | ||||
| chr9:133429130-133429414 | Common:6; Rare:33 | ||||
| chr9:134025227-134025508 | Common:17; Rare:88 | ||||
| chr9:135366070-135366318 | Common:1; Rare:48 |