Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:71448357-71448702 | Common:3; Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
chr11:71787303-71787546 | Common:15; Rare:91 | ||||
chr11:71928930-71929058 | Common:1; Rare:44 | ||||
chr11:72080232-72080341 | Common:6; Rare:15 | ||||
chr11:72080432-72080845 | Common:2; Rare:98; Clinvar:8 | ||||
chr11:73218184-73218650 | Common:1; Rare:85 | ||||
chr11:73597995-73598254 | Common:3; Rare:66 | ||||
chr11:73876778-73877027 | Common:5; Rare:68 | ||||
chr11:73982823-73982962 | Common:6; Rare:44 | ||||
chr11:74071042-74071389 | Common:1; Rare:60 | ||||
chr11:74170838-74171099 | Common:1; Rare:76 | ||||
chr11:74171158-74171427 | Common:2; Rare:91 | ||||
chr11:74493720-74493786 | Rare:22 | ||||
chr11:74949062-74949288 | Common:6; Rare:59 | ||||
chr11:75351610-75351874 | Common:3; Rare:77 |