| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34612062-34612238 | Common:9; Rare:68 | ||||
| chr9:34637716-34637953 | Rare:69 | ||||
| chr9:34646551-34646707 | Common:1; Rare:47; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr9:34652017-34652205 | Rare:53 | ||||
| chr9:34665373-34665665 | Rare:94 | ||||
| chr9:35079996-35080157 | Common:3; Rare:41; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:35101233-35101453 | Common:1; Rare:65 | ||||
| chr9:35103049-35103297 | Common:1; Rare:94 | ||||
| chr9:35489916-35490152 | Common:3; Rare:67 | ||||
| chr9:35657846-35658376 | Common:8; Rare:441; Clinvar:42; Clinvar (benign):15; Clinvar (pathogenic):40 | ||||
| chr9:35665172-35665314 | Common:1; Rare:54 | ||||
| chr9:35673854-35673962 | Common:2; Rare:31 | ||||
| chr9:35685432-35685693 | Common:1; Rare:62; Clinvar (benign):4 | ||||
| chr9:35689702-35690129 | Common:4; Rare:132; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35732076-35732344 | Common:2; Rare:75 |