| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35072492-35073018 | Rare:120; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35079926-35080157 | Common:4; Rare:58; Clinvar:3; Clinvar (benign):3 | ||||
| chr9:35103092-35103297 | Common:1; Rare:69 | ||||
| chr9:35111586-35111911 | Rare:81 | ||||
| chr9:35115803-35116161 | Common:1; Rare:69 | ||||
| chr9:35161778-35162153 | Common:4; Rare:106 | ||||
| chr9:35162278-35162325 | Rare:13 | ||||
| chr9:35489897-35490148 | Common:3; Rare:70 | ||||
| chr9:35538737-35539051 | Common:2; Rare:69 | ||||
| chr9:35657906-35658376 | Common:6; Rare:381; Clinvar:29; Clinvar (benign):13; Clinvar (pathogenic):37 | ||||
| chr9:35732083-35732306 | Common:1; Rare:61 | ||||
| chr9:35732308-35732433 | Common:1; Rare:40 | ||||
| chr9:35732447-35732676 | Common:1; Rare:61 | ||||
| chr9:35748978-35749408 | Common:3; Rare:158 | ||||
| chr9:35749689-35749762 | Rare:28 |