| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:65156401-65156798 | Common:1; Rare:61 | ||||
| chr12:65170325-65170610 | Common:1; Rare:114; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:66072258-66072362 | Rare:16 | ||||
| chr12:66196883-66197069 | Common:2; Rare:42 | ||||
| chr12:66235391-66235476 | Rare:20 | ||||
| chr12:66303595-66303829 | Common:1; Rare:44 | ||||
| chr12:66304447-66304576 | Rare:25 | ||||
| chr12:67268515-67268656 | Common:1; Rare:23 | ||||
| chr12:67698808-67699086 | Rare:44 | ||||
| chr12:67988758-67988930 | Common:2; Rare:31 | ||||
| chr12:67991277-67991466 | Common:2; Rare:35 | ||||
| chr12:68012823-68013000 | Rare:16 | ||||
| chr12:68042397-68042498 | Rare:24 | ||||
| chr12:68175556-68175715 | Common:1; Rare:26 | ||||
| chr12:68236752-68236853 | Common:1; Rare:20 |