Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:90223015-90223136 | Common:1; Rare:46 | ||||
chr11:93741485-93741714 | Common:4; Rare:78 | ||||
chr11:93784185-93784362 | Common:3; Rare:56 | ||||
chr11:94128795-94129177 | Common:3; Rare:126 | ||||
chr11:94493792-94494053 | Common:4; Rare:76; Clinvar (benign):1 | ||||
chr11:94543631-94543951 | Common:5; Rare:66 | ||||
chr11:94973524-94973719 | Rare:61 | ||||
chr11:95067457-95067573 | Rare:41 | ||||
chr11:95789766-95790118 | Common:4; Rare:115 | ||||
chr11:95790359-95790591 | Common:1; Rare:89 | ||||
chr11:95923950-95924157 | Rare:91; Clinvar (benign):1 | ||||
chr11:96389860-96390052 | Common:1; Rare:78 | ||||
chr11:101127541-101127721 | Rare:80 | ||||
chr11:101914732-101915059 | Common:3; Rare:75 | ||||
chr11:101915115-101915354 | Common:3; Rare:70 |