Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:75721075-75721556 | Common:4; Rare:132; Clinvar:2 | ||||
chr17:75779223-75779538 | Common:1; Rare:161 | ||||
chr17:75784564-75784868 | Common:2; Rare:133 | ||||
chr17:75855242-75855679 | Common:1; Rare:122 | ||||
chr17:75875977-75876241 | Rare:69 | ||||
chr17:75979008-75979276 | Rare:77; Clinvar:4 | ||||
chr17:75979358-75979587 | Common:1; Rare:69; Clinvar (benign):1 | ||||
chr17:76103695-76103867 | Common:5; Rare:60 | ||||
chr17:76384497-76384659 | Common:1; Rare:48 | ||||
chr17:76537911-76538020 | Rare:41 | ||||
chr17:76709208-76709508 | Rare:50 | ||||
chr17:76726449-76726886 | Common:5; Rare:166 | ||||
chr17:76737309-76737691 | Common:4; Rare:135 | ||||
chr17:76737864-76738043 | Common:3; Rare:50 | ||||
chr17:77127754-77127902 | Rare:26 |