| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6752917-6753189 | Common:6; Rare:80 | ||||
| chr12:6851913-6852174 | Rare:66 | ||||
| chr12:6867398-6867655 | Common:2; Rare:128; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6869101-6869384 | Rare:90; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr12:6873281-6873541 | Common:2; Rare:74 | ||||
| chr12:6904697-6904895 | Rare:43 | ||||
| chr12:6914407-6914627 | Rare:56 | ||||
| chr12:6937591-6937849 | Common:1; Rare:72 | ||||
| chr12:6943531-6943834 | Common:4; Rare:135 | ||||
| chr12:6943979-6944172 | Common:3; Rare:189; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6946277-6946585 | Common:1; Rare:81 | ||||
| chr12:6951240-6951457 | Rare:61 | ||||
| chr12:6970616-6970961 | Common:3; Rare:108 | ||||
| chr12:7018431-7018696 | Common:1; Rare:80 | ||||
| chr12:7067496-7067762 | Common:2; Rare:64; Clinvar (benign):1 |