| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:95509147-95509270 | Rare:38 | ||||
| chr9:95875453-95875703 | Common:1; Rare:82 | ||||
| chr9:95875961-95876058 | Common:5; Rare:50; Clinvar (pathogenic):1 | ||||
| chr9:96566820-96566849 | Rare:10 | ||||
| chr9:96566879-96566903 | Rare:5 | ||||
| chr9:96778054-96778154 | Rare:32 | ||||
| chr9:97039137-97039292 | Rare:57 | ||||
| chr9:97633276-97633884 | Common:6; Rare:189 | ||||
| chr9:97666490-97666805 | Common:4; Rare:51 | ||||
| chr9:97922471-97922570 | Common:3; Rare:49 | ||||
| chr9:98119105-98119287 | Common:1; Rare:57 | ||||
| chr9:98192560-98192818 | Common:5; Rare:77 | ||||
| chr9:98255355-98255397 | Common:1; Rare:10 | ||||
| chr9:98255578-98255683 | Rare:24 | ||||
| chr9:98807069-98807297 | Common:1; Rare:39 |