| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:68407538-68407653 | Rare:25 | ||||
| chr10:68471514-68471565 | Common:1; Rare:14 | ||||
| chr10:68471586-68471777 | Common:2; Rare:49 | ||||
| chr10:68471807-68472143 | Common:1; Rare:147; Clinvar (benign):2 | ||||
| chr10:68526754-68526936 | Rare:22 | ||||
| chr10:68527022-68527287 | Common:1; Rare:60; Clinvar (pathogenic):1 | ||||
| chr10:68527347-68527732 | Common:3; Rare:120 | ||||
| chr10:68561005-68561071 | Rare:9 | ||||
| chr10:68720590-68720750 | Rare:35 | ||||
| chr10:68720902-68721378 | Common:3; Rare:149 | ||||
| chr10:68721395-68721612 | Common:2; Rare:72 | ||||
| chr10:68721721-68721796 | Common:1; Rare:15 | ||||
| chr10:68827166-68827263 | Common:1; Rare:20 | ||||
| chr10:68827276-68827614 | Common:5; Rare:127 | ||||
| chr10:68900727-68901114 | Common:1; Rare:137 |