Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:64181655-64181854 | Rare:41 | ||||
chr11:64242489-64242638 | Common:1; Rare:36 | ||||
chr11:64268552-64268952 | Common:1; Rare:123 | ||||
chr11:64269023-64269423 | Common:2; Rare:133 | ||||
chr11:64301124-64301449 | Common:1; Rare:70 | ||||
chr11:64304400-64304619 | Rare:61 | ||||
chr11:64335229-64335364 | Rare:19 | ||||
chr11:64356552-64356738 | Common:1; Rare:43 | ||||
chr11:64372962-64373275 | Common:5; Rare:67 | ||||
chr11:64449627-64449869 | Rare:54 | ||||
chr11:64545731-64545838 | Common:1; Rare:18 | ||||
chr11:64566633-64566832 | Common:1; Rare:42 | ||||
chr11:64630140-64630440 | Common:1; Rare:74; Clinvar (benign):1 | ||||
chr11:64653009-64653260 | Common:1; Rare:42 | ||||
chr11:64659760-64660300 | Common:2; Rare:88 |