Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:119101774-119102106 | Rare:83; Clinvar:4 | ||||
chr11:119110603-119110918 | Rare:86 | ||||
chr11:119121310-119121626 | Common:1; Rare:69 | ||||
chr11:119206176-119206383 | Common:5; Rare:95; Clinvar:8; Clinvar (benign):4 | ||||
chr11:119317110-119317275 | Rare:57 | ||||
chr11:119334259-119334533 | Rare:73 | ||||
chr11:119381622-119381855 | Common:1; Rare:50 | ||||
chr11:119423127-119423308 | Common:2; Rare:57 | ||||
chr11:120385227-120385405 | Rare:26 | ||||
chr11:121292569-121292923 | Rare:111; Clinvar:3 | ||||
chr11:122655575-122655901 | Common:3; Rare:77 | ||||
chr11:122882813-122882968 | Rare:42 | ||||
chr11:123062360-123062663 | Common:4; Rare:141 | ||||
chr11:123509830-123510030 | Rare:46 | ||||
chr11:123560131-123560342 | Common:2; Rare:43 |