| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:132406812-132406945 | Rare:44 | ||||
| chr9:132409840-132410120 | Common:4; Rare:66 | ||||
| chr9:132669565-132669902 | Rare:109 | ||||
| chr9:132669974-132670218 | Common:2; Rare:112 | ||||
| chr9:132670399-132670525 | Rare:44 | ||||
| chr9:132878273-132878435 | Common:1; Rare:61 | ||||
| chr9:132944572-132944868 | Common:1; Rare:103; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:133030400-133030747 | Common:4; Rare:104 | ||||
| chr9:133030879-133031020 | Common:1; Rare:49 | ||||
| chr9:133149168-133149496 | Common:1; Rare:114 | ||||
| chr9:133163820-133164160 | Common:4; Rare:80 | ||||
| chr9:133336121-133336356 | Common:1; Rare:101 | ||||
| chr9:133348002-133348290 | Common:4; Rare:116 | ||||
| chr9:133356425-133356607 | Common:1; Rare:82; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:133376011-133376411 | Common:3; Rare:145 |