| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:68721320-68721580 | Common:6; Rare:183 | ||||
| chr10:68721659-68722239 | Common:7; Rare:226 | ||||
| chr10:68827285-68827685 | Common:10; Rare:255 | ||||
| chr10:68900700-68900940 | Common:3; Rare:171 | ||||
| chr10:68900963-68901686 | Common:21; Rare:1061 | ||||
| chr10:68955540-68956770 | Common:26; Rare:1234 | ||||
| chr10:68988506-68988962 | Common:8; Rare:260; Clinvar:3; Clinvar (benign):11 | ||||
| chr10:68989071-68989518 | Rare:172; Clinvar (pathogenic):1 | ||||
| chr10:69087325-69087616 | Common:11; Rare:86 | ||||
| chr10:69087690-69088280 | Common:3; Rare:419 | ||||
| chr10:69123172-69123572 | Common:7; Rare:135 | ||||
| chr10:69123476-69124320 | Common:17; Rare:757 | ||||
| chr10:69124470-69124810 | Common:4; Rare:174 | ||||
| chr10:69179590-69180400 | Common:24; Rare:1003 | ||||
| chr10:69180482-69181077 | Common:8; Rare:218 |