| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:68467274-68467594 | Common:1; Rare:77 | ||||
| chr2:69387065-69387398 | Common:1; Rare:96; Clinvar:3 | ||||
| chr2:69437395-69437549 | Rare:75; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:69643591-69643834 | Rare:85 | ||||
| chr2:69829517-69829737 | Common:1; Rare:87 | ||||
| chr2:69914767-69915129 | Common:1; Rare:94 | ||||
| chr2:70087307-70087873 | Common:2; Rare:204 | ||||
| chr2:70248426-70248795 | Common:4; Rare:151; Clinvar:1 | ||||
| chr2:70257682-70257745 | Common:2; Rare:8 | ||||
| chr2:70258019-70258274 | Common:2; Rare:89 | ||||
| chr2:70293650-70293848 | Common:2; Rare:68 | ||||
| chr2:70301936-70302189 | Common:5; Rare:119 | ||||
| chr2:70994779-70994968 | Common:3; Rare:66 | ||||
| chr2:71068538-71068686 | Rare:64 | ||||
| chr2:71130220-71130674 | Common:6; Rare:129; Clinvar:1; Clinvar (benign):2 |