| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:132878251-132878418 | Common:1; Rare:69 | ||||
| chr9:132878806-132878975 | Rare:30 | ||||
| chr9:132944485-132944984 | Common:1; Rare:174; Clinvar:3; Clinvar (benign):4 | ||||
| chr9:132945371-132945539 | Common:2; Rare:27 | ||||
| chr9:133030447-133030742 | Common:4; Rare:78 | ||||
| chr9:133030925-133031030 | Rare:40 | ||||
| chr9:133163910-133164047 | Common:3; Rare:34 | ||||
| chr9:133209201-133209410 | Common:1; Rare:33 | ||||
| chr9:133275181-133275302 | Rare:25 | ||||
| chr9:133336106-133336290 | Common:1; Rare:80 | ||||
| chr9:133348039-133348386 | Common:3; Rare:147 | ||||
| chr9:133348458-133348663 | Common:6; Rare:66 | ||||
| chr9:133356425-133356640 | Common:1; Rare:102; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:133375480-133375586 | Rare:25 | ||||
| chr9:133375965-133376474 | Common:6; Rare:197 |