| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6723796-6724172 | Common:1; Rare:81 | ||||
| chr12:6724213-6724296 | Rare:14 | ||||
| chr12:6752908-6753189 | Common:6; Rare:80 | ||||
| chr12:6821472-6821819 | Common:2; Rare:80 | ||||
| chr12:6849741-6850024 | Common:2; Rare:61 | ||||
| chr12:6851902-6852186 | Rare:73 | ||||
| chr12:6867379-6867615 | Common:2; Rare:118; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6869677-6870029 | Common:4; Rare:90; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr12:6870046-6870486 | Common:1; Rare:150; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6873282-6873664 | Common:4; Rare:112 | ||||
| chr12:6927580-6927818 | Rare:60 | ||||
| chr12:6937474-6937742 | Common:1; Rare:77 | ||||
| chr12:6943517-6943830 | Common:4; Rare:139 | ||||
| chr12:6943926-6944172 | Common:8; Rare:246; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6944195-6944504 | Common:2; Rare:139; Clinvar:3; Clinvar (pathogenic):1 |