| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6534327-6534582 | Common:5; Rare:111 | ||||
| chr12:6568241-6568384 | Rare:57 | ||||
| chr12:6606369-6606734 | Common:3; Rare:138 | ||||
| chr12:6607008-6607122 | Rare:37 | ||||
| chr12:6663085-6663364 | Common:1; Rare:81 | ||||
| chr12:6688893-6689089 | Rare:64 | ||||
| chr12:6689454-6689756 | Common:2; Rare:78 | ||||
| chr12:6723828-6724311 | Common:2; Rare:108 | ||||
| chr12:6752684-6752791 | Common:1; Rare:23 | ||||
| chr12:6752917-6753205 | Common:6; Rare:88 | ||||
| chr12:6821405-6821640 | Common:2; Rare:57 | ||||
| chr12:6829650-6829686 | Rare:5 | ||||
| chr12:6851239-6851497 | Rare:61 | ||||
| chr12:6851877-6852182 | Rare:81 | ||||
| chr12:6867365-6867675 | Common:2; Rare:146; Clinvar:2; Clinvar (benign):2 |