chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
137022817470228175GA19GENIChomozygous962036658
137022863870228639CT12GENIChomozygous962036659
137022897870228979GA29GENIChomozygous962036660
137022933670229337GT25GENIChomozygous962036661
137022936170229362GC21GENIChomozygous962036662
137022975170229752TC23GENIChomozygous962036663
137023245470232455AT15GENIChomozygous962036664
137023313870233139TC22GENIChomozygous962036665
137023329170233292TC25GENIChomozygous962036666
137023449870234499AG27GENIChomozygous962036667
137023488070234881CT11GENIChomozygous962036668
137023525870235259AG26GENIChomozygous962036669
137023609770236098AG21GENIChomozygous962036670
137024025270240253CG17GENIChomozygous962036671
137024124770241248GA10GENIChomozygous962036672
137024211070242111TC22GENIChomozygous962036673
137024423570244236CG29GENIChomozygous962036674
137024604770246048TC23GENIChomozygous962036675
137024620870246209TC27GENIChomozygous962036676
137024646670246467AG28GENICpossibly homozygous962036677
137024651770246518AC29GENIChomozygous962036678
137024651870246519GT30GENIChomozygous962036679
137024952070249521GA38GENIChomozygous962036680
137024997870249979AG41GENIChomozygous962036681
137025215470252155TC23GENIChomozygous962036682
137025324070253241CA18GENIChomozygous962036683
137025353070253531CT26GENIChomozygous962036684
137025500070255001AG32GENIChomozygous962036685
137025617270256173GT22GENIChomozygous962036686
137025888170258882GA24GENIChomozygous962036687