Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:63838835-63838905 | Common:1; Rare:31 | ||||
chr11:64226091-64226327 | Common:3; Rare:68 | ||||
chr11:64240890-64241139 | Rare:67 | ||||
chr11:64245359-64245982 | Common:4; Rare:135 | ||||
chr11:64246233-64246321 | Rare:20 | ||||
chr11:64284637-64284869 | Common:1; Rare:104 | ||||
chr11:64317092-64317353 | Rare:117 | ||||
chr11:64317447-64317638 | Common:3; Rare:69 | ||||
chr11:64318066-64318384 | Common:1; Rare:141 | ||||
chr11:64359083-64359184 | Rare:23 | ||||
chr11:64753518-64754347 | Common:3; Rare:267; Clinvar:20; Clinvar (benign):9; Clinvar (pathogenic):6 | ||||
chr11:64759656-64760050 | Rare:133; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):7 | ||||
chr11:64778760-64779026 | Common:3; Rare:88 | ||||
chr11:64917187-64917573 | Common:3; Rare:88 | ||||
chr11:65014025-65014268 | Rare:61 |