Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:62646569-62646809 | Common:1; Rare:96; Clinvar (pathogenic):1 | ||||
chr11:62665143-62665317 | Common:4; Rare:80 | ||||
chr11:62709497-62709727 | Common:1; Rare:97 | ||||
chr11:62728410-62728794 | Common:3; Rare:174 | ||||
chr11:62787329-62787434 | Common:2; Rare:75 | ||||
chr11:62791970-62792094 | Common:1; Rare:66 | ||||
chr11:62797253-62797371 | Rare:38 | ||||
chr11:62825192-62825467 | Common:1; Rare:73 | ||||
chr11:62831620-62831924 | Common:2; Rare:91 | ||||
chr11:62832011-62832297 | Common:1; Rare:105 | ||||
chr11:62841951-62842097 | Common:1; Rare:48 | ||||
chr11:62855862-62856087 | Rare:96 | ||||
chr11:62880607-62880927 | Common:1; Rare:74 | ||||
chr11:64166129-64166238 | Rare:30 | ||||
chr11:64197349-64197494 | Common:1; Rare:30 |