Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:809878-810037 | Common:2; Rare:78 | ||||
chr11:842483-842915 | Common:7; Rare:184 | ||||
chr11:843964-844141 | Common:1; Rare:43 | ||||
chr11:1309617-1309838 | Common:1; Rare:93 | ||||
chr11:1919444-1919737 | Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
chr11:1933791-1934005 | Rare:80; Clinvar:1; Clinvar (benign):2 | ||||
chr11:2138510-2138579 | Common:1; Rare:14 | ||||
chr11:2138897-2139041 | Common:1; Rare:22 | ||||
chr11:4393654-4393826 | Rare:41 | ||||
chr11:5624894-5625005 | Rare:14 | ||||
chr11:6320490-6320615 | Common:2; Rare:43 | ||||
chr11:6390237-6390517 | Common:2; Rare:82 | ||||
chr11:6473889-6474100 | Rare:68 | ||||
chr11:6481285-6481524 | Common:4; Rare:94 | ||||
chr11:6603577-6603831 | Common:2; Rare:78; Clinvar (benign):3 |