| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35689683-35690156 | Common:4; Rare:145; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35690216-35690496 | Common:1; Rare:67 | ||||
| chr9:35690610-35690977 | Common:1; Rare:78 | ||||
| chr9:35691063-35691265 | Common:1; Rare:43 | ||||
| chr9:35698806-35699067 | Common:1; Rare:70 | ||||
| chr9:35704315-35704814 | Common:1; Rare:117 | ||||
| chr9:35705540-35706369 | Common:4; Rare:200 | ||||
| chr9:35706448-35707254 | Common:2; Rare:218 | ||||
| chr9:35731943-35732355 | Common:2; Rare:112 | ||||
| chr9:35732365-35732794 | Common:4; Rare:110 | ||||
| chr9:35748994-35749395 | Common:2; Rare:150 | ||||
| chr9:35814975-35815299 | Rare:82 | ||||
| chr9:35829072-35829290 | Common:1; Rare:57 | ||||
| chr9:35906031-35906287 | Rare:63 | ||||
| chr9:36190757-36191068 | Common:1; Rare:95 |