| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6568260-6568393 | Rare:52 | ||||
| chr12:6606293-6606591 | Common:4; Rare:122 | ||||
| chr12:6606623-6606907 | Rare:96 | ||||
| chr12:6688888-6689089 | Rare:66 | ||||
| chr12:6689091-6689340 | Rare:69 | ||||
| chr12:6689381-6689754 | Common:3; Rare:100 | ||||
| chr12:6723855-6724295 | Common:1; Rare:93 | ||||
| chr12:6752937-6753189 | Common:6; Rare:77 | ||||
| chr12:6766422-6766748 | Rare:88 | ||||
| chr12:6851269-6851472 | Rare:42 | ||||
| chr12:6851902-6852174 | Rare:70 | ||||
| chr12:6867353-6867653 | Common:2; Rare:144; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6869094-6869399 | Rare:96; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr12:6869428-6869744 | Common:1; Rare:90; Clinvar (pathogenic):1 | ||||
| chr12:6870052-6870327 | Common:1; Rare:80; Clinvar:1; Clinvar (benign):1 |