| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:62260032-62260424 | Common:1; Rare:142 | ||||
| chr12:63780018-63780170 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr12:64222241-64222369 | Rare:42 | ||||
| chr12:64404167-64404681 | Common:6; Rare:180 | ||||
| chr12:64452041-64452174 | Common:1; Rare:48 | ||||
| chr12:64759373-64759501 | Common:1; Rare:42; Clinvar:3 | ||||
| chr12:65169441-65169602 | Common:1; Rare:50; Clinvar:1 | ||||
| chr12:66130718-66130821 | Rare:35 | ||||
| chr12:66302314-66302596 | Common:1; Rare:65 | ||||
| chr12:68332265-68332615 | Common:1; Rare:115 | ||||
| chr12:68610733-68611014 | Common:1; Rare:118 | ||||
| chr12:68686835-68687000 | Common:3; Rare:44 | ||||
| chr12:69239448-69239656 | Common:2; Rare:89 | ||||
| chr12:69470288-69470450 | Common:3; Rare:64 | ||||
| chr12:69585308-69585516 | Common:3; Rare:84 |