| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33264718-33265085 | Rare:95 | ||||
| chr9:33290280-33290563 | Common:2; Rare:99 | ||||
| chr9:33473862-33474138 | Common:2; Rare:82 | ||||
| chr9:34048866-34048966 | Rare:42 | ||||
| chr9:34049186-34049293 | Common:1; Rare:27 | ||||
| chr9:34178937-34179078 | Common:1; Rare:39 | ||||
| chr9:34329186-34329620 | Common:1; Rare:137 | ||||
| chr9:34651992-34652217 | Rare:69 | ||||
| chr9:34665364-34665665 | Rare:96 | ||||
| chr9:35071975-35072150 | Common:1; Rare:54 | ||||
| chr9:35489924-35490152 | Common:3; Rare:64 | ||||
| chr9:35657857-35658376 | Common:8; Rare:433; Clinvar:41; Clinvar (benign):15; Clinvar (pathogenic):40 | ||||
| chr9:35689702-35689969 | Common:3; Rare:86; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35731964-35732676 | Common:4; Rare:189 | ||||
| chr9:35748965-35749347 | Common:2; Rare:140 |