Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:22625457-22625595 | Common:1; Rare:61; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr11:22625657-22626019 | Common:4; Rare:141; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr11:27362840-27363141 | Common:2; Rare:129 | ||||
chr11:27472665-27472960 | Common:1; Rare:72 | ||||
chr11:27506718-27506863 | Common:1; Rare:67 | ||||
chr11:27700405-27700522 | Common:1; Rare:35 | ||||
chr11:27722009-27722367 | Rare:67 | ||||
chr11:28108072-28108424 | Common:2; Rare:104 | ||||
chr11:30322944-30323201 | Common:2; Rare:73 | ||||
chr11:30586339-30586519 | Common:1; Rare:41 | ||||
chr11:31369724-31369940 | Rare:67 | ||||
chr11:31509536-31509940 | Common:2; Rare:149 | ||||
chr11:32090810-32091167 | Common:3; Rare:107 | ||||
chr11:32583629-32583927 | Rare:105 | ||||
chr11:32830328-32830416 | Rare:24 |