Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:695720-695817 | Rare:34 | ||||
chr11:747299-747493 | Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
chr11:777460-777598 | Common:1; Rare:61 | ||||
chr11:790063-790173 | Common:1; Rare:30 | ||||
chr11:809870-810038 | Common:2; Rare:82 | ||||
chr11:832832-833008 | Common:7; Rare:58 | ||||
chr11:842478-842886 | Common:7; Rare:171 | ||||
chr11:925701-925990 | Common:3; Rare:126 | ||||
chr11:1309554-1309851 | Common:3; Rare:124 | ||||
chr11:3057369-3057538 | Rare:59 | ||||
chr11:3379089-3379309 | Common:3; Rare:58 | ||||
chr11:3797476-3797929 | Rare:174 | ||||
chr11:4094737-4094897 | Common:1; Rare:49 | ||||
chr11:6234625-6234798 | Common:2; Rare:53 | ||||
chr11:6390272-6390482 | Common:2; Rare:61 |