| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:95875449-95875707 | Common:1; Rare:87 | ||||
| chr9:95875965-95876084 | Common:5; Rare:59; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:96655300-96655434 | Rare:34 | ||||
| chr9:96778046-96778156 | Rare:36 | ||||
| chr9:97039079-97039229 | Rare:59 | ||||
| chr9:97633113-97633860 | Common:6; Rare:226 | ||||
| chr9:97922176-97922280 | Common:1; Rare:32 | ||||
| chr9:97922443-97922609 | Common:3; Rare:84 | ||||
| chr9:97983106-97983607 | Common:2; Rare:187 | ||||
| chr9:97984239-97984607 | Common:1; Rare:155 | ||||
| chr9:98056531-98056831 | Common:2; Rare:105 | ||||
| chr9:98119186-98119283 | Common:1; Rare:26 | ||||
| chr9:98192623-98192860 | Common:6; Rare:64 | ||||
| chr9:98255354-98255516 | Common:1; Rare:53 | ||||
| chr9:98255581-98255814 | Common:3; Rare:70 |