| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6752937-6753194 | Common:6; Rare:81 | ||||
| chr12:6851243-6851461 | Rare:52 | ||||
| chr12:6851902-6852181 | Rare:73 | ||||
| chr12:6867361-6867680 | Common:2; Rare:149; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6870045-6870589 | Common:1; Rare:182; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6873282-6873546 | Common:2; Rare:76 | ||||
| chr12:6943517-6943824 | Common:4; Rare:133 | ||||
| chr12:6943979-6944172 | Common:3; Rare:189; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6946262-6946635 | Common:1; Rare:93 | ||||
| chr12:6970461-6970988 | Common:4; Rare:169; Clinvar (benign):1 | ||||
| chr12:7060390-7060883 | Rare:97 | ||||
| chr12:7091762-7092050 | Common:1; Rare:77 | ||||
| chr12:7099670-7100022 | Common:2; Rare:97 | ||||
| chr12:7108410-7108657 | Common:1; Rare:78 | ||||
| chr12:7128828-7129208 | Common:2; Rare:49 |