| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34652015-34652200 | Rare:52 | ||||
| chr9:34665363-34665660 | Rare:96 | ||||
| chr9:34710023-34710253 | Common:1; Rare:41 | ||||
| chr9:35161827-35162149 | Common:4; Rare:92 | ||||
| chr9:35489802-35490108 | Common:1; Rare:96 | ||||
| chr9:35657836-35658431 | Common:12; Rare:474; Clinvar:44; Clinvar (benign):17; Clinvar (pathogenic):40 | ||||
| chr9:35689702-35690113 | Common:4; Rare:128; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35732073-35732320 | Common:1; Rare:66 | ||||
| chr9:35732373-35732677 | Common:3; Rare:76 | ||||
| chr9:35748982-35749361 | Common:2; Rare:142 | ||||
| chr9:36136614-36136791 | Common:2; Rare:53 | ||||
| chr9:37904354-37904462 | Rare:38 | ||||
| chr9:43127079-43127436 | Common:2; Rare:98 | ||||
| chr9:65675716-65675964 | Rare:60 | ||||
| chr9:68356388-68356628 | Common:7; Rare:42 |