| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35489922-35490121 | Common:1; Rare:56 | ||||
| chr9:35657950-35658369 | Common:6; Rare:324; Clinvar:24; Clinvar (benign):12; Clinvar (pathogenic):35 | ||||
| chr9:35732083-35732320 | Common:1; Rare:66 | ||||
| chr9:35732373-35732700 | Common:3; Rare:83 | ||||
| chr9:35748978-35749369 | Common:2; Rare:145 | ||||
| chr9:35814984-35815293 | Rare:79 | ||||
| chr9:37785009-37785124 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):3 | ||||
| chr9:37800723-37800773 | Rare:14 | ||||
| chr9:37904079-37904222 | Rare:46 | ||||
| chr9:66900567-66900804 | Common:3; Rare:77 | ||||
| chr9:69759939-69760143 | Common:3; Rare:92 | ||||
| chr9:70258848-70259077 | Common:3; Rare:105 | ||||
| chr9:75088140-75088532 | Common:3; Rare:133 | ||||
| chr9:77177441-77177567 | Common:2; Rare:39; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:78236001-78236289 | Common:1; Rare:91 |