| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:88388225-88388537 | Common:1; Rare:131 | ||||
| chr9:89310910-89311216 | Common:3; Rare:94 | ||||
| chr9:89318415-89318561 | Common:5; Rare:70 | ||||
| chr9:91950146-91950414 | Common:2; Rare:77 | ||||
| chr9:92115339-92115509 | Common:1; Rare:55; Clinvar:1 | ||||
| chr9:92293665-92293849 | Common:3; Rare:65 | ||||
| chr9:92325316-92325973 | Common:8; Rare:176 | ||||
| chr9:92670053-92670345 | Common:1; Rare:87 | ||||
| chr9:93451454-93451702 | Common:3; Rare:70 | ||||
| chr9:93452330-93452383 | Rare:8 | ||||
| chr9:93452919-93453202 | Rare:60 | ||||
| chr9:93453546-93453665 | Rare:24 | ||||
| chr9:95317655-95317799 | Common:1; Rare:49; Clinvar:2 | ||||
| chr9:95505863-95506188 | Common:1; Rare:114 | ||||
| chr9:95506574-95506672 | Rare:42; Clinvar:5; Clinvar (benign):5 |