| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33025093-33025367 | Common:6; Rare:116 | ||||
| chr9:33076615-33076854 | Common:2; Rare:80 | ||||
| chr9:33264696-33265119 | Rare:117 | ||||
| chr9:33473844-33474140 | Common:4; Rare:91 | ||||
| chr9:34049186-34049263 | Common:1; Rare:19 | ||||
| chr9:34329233-34329593 | Rare:107 | ||||
| chr9:34637739-34638127 | Common:3; Rare:99 | ||||
| chr9:35657985-35658354 | Common:6; Rare:274; Clinvar:18; Clinvar (benign):10; Clinvar (pathogenic):33 | ||||
| chr9:35689705-35690042 | Common:3; Rare:113; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35732083-35732718 | Common:5; Rare:176 | ||||
| chr9:35748910-35749342 | Common:3; Rare:146 | ||||
| chr9:35814984-35815340 | Common:1; Rare:90 | ||||
| chr9:37800697-37800924 | Common:1; Rare:78 | ||||
| chr9:37904034-37904234 | Rare:64 | ||||
| chr9:37904342-37904648 | Rare:84 |