| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:86282051-86282326 | Common:4; Rare:93 | ||||
| chr9:86282476-86282647 | Common:3; Rare:86 | ||||
| chr9:86353999-86354643 | Common:1; Rare:208 | ||||
| chr9:87725903-87726396 | Common:6; Rare:123 | ||||
| chr9:87974495-87974848 | Common:3; Rare:101 | ||||
| chr9:88388224-88388504 | Common:1; Rare:120 | ||||
| chr9:89310910-89311290 | Common:3; Rare:148 | ||||
| chr9:89318342-89318597 | Common:6; Rare:108 | ||||
| chr9:91361709-91362028 | Common:2; Rare:115; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr9:92115339-92115509 | Common:1; Rare:55; Clinvar:1 | ||||
| chr9:92293523-92293962 | Common:7; Rare:135 | ||||
| chr9:92310644-92310776 | Rare:33 | ||||
| chr9:92325299-92326001 | Common:9; Rare:191 | ||||
| chr9:92669989-92670429 | Common:1; Rare:144 | ||||
| chr9:92764770-92765084 | Common:2; Rare:105; Clinvar (benign):2 |