Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:119334285-119334529 | Rare:67 | ||||
chr11:119381607-119381819 | Common:1; Rare:43 | ||||
chr11:119423149-119423537 | Common:6; Rare:90 | ||||
chr11:121292569-121292883 | Rare:106; Clinvar:3 | ||||
chr11:122655575-122655807 | Common:2; Rare:57 | ||||
chr11:122656119-122656132 | Rare:5 | ||||
chr11:123062075-123062306 | Common:3; Rare:92 | ||||
chr11:123062434-123062686 | Common:2; Rare:111 | ||||
chr11:123509787-123509939 | Rare:42 | ||||
chr11:123525840-123525954 | Common:1; Rare:32 | ||||
chr11:123560226-123560331 | Rare:16 | ||||
chr11:123654552-123654797 | Common:5; Rare:64; Clinvar (benign):1 | ||||
chr11:123741575-123741807 | Common:2; Rare:65 | ||||
chr11:124622578-124622891 | Common:5; Rare:88 | ||||
chr11:124673715-124673808 | Rare:38 |