| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:8964378-8964541 | Common:3; Rare:48 | ||||
| chr11:10541145-10541293 | Rare:52 | ||||
| chr11:10800205-10800534 | Rare:84 | ||||
| chr11:14513604-14513858 | Rare:58 | ||||
| chr11:18322180-18322308 | Common:1; Rare:42 | ||||
| chr11:18526851-18526966 | Rare:58 | ||||
| chr11:18588654-18588839 | Common:2; Rare:66 | ||||
| chr11:20387447-20387758 | Common:7; Rare:104 | ||||
| chr11:31509628-31509783 | Common:1; Rare:48 | ||||
| chr11:34916315-34916618 | Common:8; Rare:124; Clinvar:3; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr11:46700568-46700785 | Common:1; Rare:56 | ||||
| chr11:46846247-46846461 | Common:1; Rare:62 | ||||
| chr11:47248791-47248947 | Rare:64 | ||||
| chr11:47565521-47565620 | Common:2; Rare:18 | ||||
| chr11:47578968-47579103 | Rare:69; Clinvar:2; Clinvar (pathogenic):1 |