| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:64771806-64772123 | Common:1; Rare:68 | ||||
| chr11:64777686-64778000 | Common:1; Rare:141 | ||||
| chr11:64778405-64778821 | Common:3; Rare:182 | ||||
| chr11:64803142-64803443 | Rare:117 | ||||
| chr11:64803666-64803906 | Rare:62; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:64810485-64810773 | Common:2; Rare:68; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:64844596-64844919 | Common:4; Rare:90 | ||||
| chr11:64859423-64859812 | Common:4; Rare:65 | ||||
| chr11:64875075-64875212 | Rare:32 | ||||
| chr11:64875444-64875636 | Rare:32 | ||||
| chr11:64876023-64876064 | Rare:7 | ||||
| chr11:64877484-64877628 | Common:1; Rare:23 | ||||
| chr11:64878501-64879127 | Common:4; Rare:199 | ||||
| chr11:64887950-64888173 | Common:1; Rare:63 | ||||
| chr11:64917136-64917623 | Common:3; Rare:125 |