Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:58326875-58327048 | Common:1; Rare:42 | ||||
chr19:58327220-58327336 | Rare:29 | ||||
chr19:58347576-58347780 | Common:8; Rare:97 | ||||
chr19:58408449-58408686 | Common:3; Rare:74 | ||||
chr19:58440134-58440457 | Common:6; Rare:88 | ||||
chr19:58451458-58451629 | Common:1; Rare:58 | ||||
chr19:58499200-58499526 | Common:3; Rare:101; Clinvar:3; Clinvar (benign):1 | ||||
chr19:58519771-58520029 | Rare:70 | ||||
chr19:58554933-58555255 | Common:2; Rare:114 | ||||
chr19:58558907-58559155 | Common:1; Rare:77 | ||||
chr2:677357-677518 | Common:1; Rare:64 | ||||
chr2:1373664-1373974 | Common:3; Rare:71 | ||||
chr2:3377796-3377953 | Rare:41 | ||||
chr2:3379625-3379787 | Common:2; Rare:67 | ||||
chr2:3519415-3519660 | Common:2; Rare:73 |