Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:62626112-62626344 | Rare:66 | ||||
chr11:62665143-62665312 | Common:3; Rare:75 | ||||
chr11:62671754-62671972 | Common:1; Rare:83; Clinvar (benign):1 | ||||
chr11:62691075-62691336 | Common:1; Rare:88; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
chr11:62726669-62726973 | Rare:144 | ||||
chr11:62727455-62727697 | Rare:92 | ||||
chr11:62728379-62728538 | Common:2; Rare:83 | ||||
chr11:62787344-62787467 | Common:1; Rare:90 | ||||
chr11:62832033-62832244 | Rare:72 | ||||
chr11:62855882-62856162 | Rare:104 | ||||
chr11:63986764-63986873 | Common:1; Rare:28 | ||||
chr11:64165942-64166239 | Common:1; Rare:84 | ||||
chr11:64197271-64197595 | Common:1; Rare:80 | ||||
chr11:64226075-64226334 | Common:3; Rare:72 | ||||
chr11:64241297-64241695 | Rare:89 |