| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:62466518-62467058 | Common:2; Rare:131 | ||||
| chr12:63779780-63779881 | Common:2; Rare:35 | ||||
| chr12:64222242-64222355 | Rare:39 | ||||
| chr12:64404232-64404669 | Common:5; Rare:156 | ||||
| chr12:64452041-64452179 | Common:1; Rare:50 | ||||
| chr12:64610285-64610651 | Common:4; Rare:128 | ||||
| chr12:64759100-64759136 | Rare:12 | ||||
| chr12:64759141-64759501 | Common:1; Rare:111; Clinvar:6; Clinvar (benign):2 | ||||
| chr12:64780689-64780827 | Rare:33 | ||||
| chr12:65169380-65169605 | Common:1; Rare:71; Clinvar:1 | ||||
| chr12:65278460-65278752 | Common:2; Rare:85 | ||||
| chr12:65824924-65825099 | Rare:38 | ||||
| chr12:66130668-66130886 | Common:1; Rare:72 | ||||
| chr12:66189032-66189399 | Rare:111; Clinvar:1 | ||||
| chr12:67269149-67269665 | Common:2; Rare:150 |