| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:64610258-64610746 | Common:7; Rare:170 | ||||
| chr12:64759109-64759472 | Rare:115; Clinvar:6; Clinvar (benign):2 | ||||
| chr12:64780570-64780818 | Common:2; Rare:64 | ||||
| chr12:65121043-65121402 | Common:1; Rare:98 | ||||
| chr12:65169380-65169602 | Common:1; Rare:70; Clinvar:1 | ||||
| chr12:65169678-65169990 | Common:2; Rare:117; Clinvar:5; Clinvar (benign):3 | ||||
| chr12:66130703-66130862 | Rare:57 | ||||
| chr12:66189005-66189375 | Rare:106; Clinvar:1 | ||||
| chr12:67269149-67269443 | Common:2; Rare:86 | ||||
| chr12:67269524-67269718 | Common:1; Rare:70 | ||||
| chr12:68332265-68332610 | Common:1; Rare:113 | ||||
| chr12:68610716-68611041 | Common:1; Rare:135 | ||||
| chr12:68686819-68687034 | Common:4; Rare:64 | ||||
| chr12:68808046-68808249 | Common:2; Rare:69 | ||||
| chr12:68808472-68808476 |