Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:76860688-76860946 | Common:3; Rare:81 | ||||
chr11:77473558-77473788 | Common:1; Rare:86 | ||||
chr11:77637711-77637868 | Common:1; Rare:57 | ||||
chr11:77820944-77821210 | Common:1; Rare:83 | ||||
chr11:78139590-78139815 | Common:3; Rare:89; Clinvar:2 | ||||
chr11:78188592-78188917 | Common:2; Rare:104 | ||||
chr11:78574768-78574964 | Common:2; Rare:77; Clinvar (benign):1 | ||||
chr11:83071815-83072124 | Common:4; Rare:85 | ||||
chr11:83193621-83193786 | Common:1; Rare:75 | ||||
chr11:83285898-83286130 | Common:3; Rare:106 | ||||
chr11:85628339-85628653 | Common:6; Rare:106 | ||||
chr11:85647875-85648036 | Common:1; Rare:40; Clinvar:2; Clinvar (benign):1 | ||||
chr11:86244441-86244786 | Common:1; Rare:88 | ||||
chr11:86244941-86245280 | Common:1; Rare:148 | ||||
chr11:86800303-86800608 | Common:2; Rare:110 |