| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6723844-6724135 | Common:1; Rare:58 | ||||
| chr12:6753063-6753189 | Common:4; Rare:47 | ||||
| chr12:6767402-6767700 | Common:2; Rare:80 | ||||
| chr12:6851922-6852174 | Rare:63 | ||||
| chr12:6867371-6867561 | Common:2; Rare:88; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6873344-6873541 | Common:1; Rare:53 | ||||
| chr12:6914408-6914659 | Common:2; Rare:66 | ||||
| chr12:6943531-6943818 | Common:4; Rare:117 | ||||
| chr12:6943938-6944124 | Common:5; Rare:192; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr12:6970621-6970961 | Common:3; Rare:107 | ||||
| chr12:7018467-7018554 | Rare:23 | ||||
| chr12:7189519-7189723 | Rare:70; Clinvar:4 | ||||
| chr12:7936167-7936443 | Common:4; Rare:44 | ||||
| chr12:8227558-8227691 | Rare:32 | ||||
| chr12:8697797-8698128 | Common:2; Rare:116 |