| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6943462-6944448 | Common:21; Rare:655; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:6944449-6944510 | Rare:29; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6944577-6944985 | Common:3; Rare:127; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:6946171-6946294 | Common:1; Rare:23 | ||||
| chr12:6946315-6946529 | Common:1; Rare:59 | ||||
| chr12:6946549-6946812 | Common:1; Rare:93 | ||||
| chr12:6951190-6951506 | Common:1; Rare:91 | ||||
| chr12:6959041-6959400 | Common:1; Rare:72 | ||||
| chr12:6959445-6959729 | Common:2; Rare:53 | ||||
| chr12:6970145-6970191 | Rare:16 | ||||
| chr12:6970519-6970991 | Common:4; Rare:152; Clinvar (benign):1 | ||||
| chr12:7018396-7019061 | Common:5; Rare:184 | ||||
| chr12:7107711-7108060 | Rare:53 | ||||
| chr12:7108338-7108712 | Common:2; Rare:110 | ||||
| chr12:7108941-7109137 | Common:13; Rare:58 |