| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34612062-34612247 | Common:9; Rare:72 | ||||
| chr9:34620447-34620589 | Common:1; Rare:43 | ||||
| chr9:34637709-34637953 | Rare:73 | ||||
| chr9:34652010-34652217 | Rare:59 | ||||
| chr9:34665373-34665662 | Rare:94 | ||||
| chr9:35072494-35072733 | Rare:62; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35079652-35079835 | Rare:33 | ||||
| chr9:35079908-35080164 | Common:5; Rare:68; Clinvar:3; Clinvar (benign):4 | ||||
| chr9:35095977-35096322 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:35101133-35101453 | Common:1; Rare:88 | ||||
| chr9:35103078-35103207 | Common:1; Rare:46 | ||||
| chr9:35161813-35162133 | Common:4; Rare:91 | ||||
| chr9:35489922-35490139 | Common:2; Rare:61 | ||||
| chr9:35646835-35646951 | Rare:24 | ||||
| chr9:35657863-35658412 | Common:9; Rare:446; Clinvar:39; Clinvar (benign):14; Clinvar (pathogenic):40 |