Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:47553012-47553277 | Common:3; Rare:101 | ||||
chr11:47565490-47565620 | Common:3; Rare:26 | ||||
chr11:47578952-47579089 | Rare:70; Clinvar:2 | ||||
chr11:57324867-57325148 | Common:2; Rare:90 | ||||
chr11:57530701-57530906 | Common:1; Rare:61 | ||||
chr11:57567618-57567867 | Rare:73 | ||||
chr11:57597413-57597747 | Rare:72; Clinvar:4; Clinvar (benign):1 | ||||
chr11:57712175-57712637 | Common:9; Rare:156 | ||||
chr11:58578085-58578157 | Rare:20 | ||||
chr11:58578819-58579216 | Common:6; Rare:114 | ||||
chr11:59142693-59142940 | Common:1; Rare:44 | ||||
chr11:60906514-60906729 | Rare:57 | ||||
chr11:60914002-60914244 | Common:1; Rare:63 | ||||
chr11:61333038-61333266 | Rare:80 | ||||
chr11:61361830-61362049 | Common:2; Rare:53; Clinvar:2 |