| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35162289-35162326 | Rare:10 | ||||
| chr9:35657841-35658403 | Common:11; Rare:459; Clinvar:42; Clinvar (benign):16; Clinvar (pathogenic):40 | ||||
| chr9:35732083-35732334 | Common:2; Rare:70 | ||||
| chr9:35732358-35732684 | Common:3; Rare:84 | ||||
| chr9:35748958-35749358 | Common:2; Rare:145 | ||||
| chr9:35812242-35812283 | Rare:15 | ||||
| chr9:35814983-35815293 | Rare:79 | ||||
| chr9:36190725-36190985 | Common:1; Rare:85 | ||||
| chr9:36258409-36258601 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:37120363-37120614 | Common:2; Rare:93 | ||||
| chr9:37785036-37785149 | Common:1; Rare:44; Clinvar (benign):2 | ||||
| chr9:37800707-37800794 | Rare:25 | ||||
| chr9:37904066-37904441 | Common:3; Rare:126 | ||||
| chr9:38620590-38620793 | Common:2; Rare:59 | ||||
| chr9:43127097-43127377 | Common:2; Rare:79 |