chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
137022817470228175GA19GENIChomozygous986140745
137022863870228639CT4GENIChomozygous986140746
137022897870228979GA8GENIChomozygous986140747
137022933670229337GT12GENIChomozygous986140748
137022936170229362GC17GENIChomozygous986140749
137022975170229752TC16GENIChomozygous986140750
137023245470232455AT12GENIChomozygous986140751
137023313870233139TC31GENIChomozygous986140752
137023329170233292TC26GENIChomozygous986140753
137023449870234499AG5GENIChomozygous986140754
137023488070234881CT15GENIChomozygous986140755
137023525870235259AG21GENIChomozygous986140756
137023609770236098AG31GENIChomozygous986140757
137024025270240253CG12GENIChomozygous986140758
137024124770241248GA16GENIChomozygous986140759
137024211070242111TC21GENIChomozygous986140760
137024604770246048TC18GENIChomozygous986140761
137024620870246209TC24GENIChomozygous986140762
137024651770246518AC21GENIChomozygous986140763
137024651870246519GT21GENIChomozygous986140764
137024887370248874GA22GENIChomozygous986140765
137024952070249521GA16GENIChomozygous986140766
137024997870249979AG20GENIChomozygous986140767
137025215470252155TC15GENIChomozygous986140768
137025324070253241CA3GENIChomozygous986140769
137025353070253531CT8GENIChomozygous986140770
137025500070255001AG25GENIChomozygous986140771
137025617270256173GT12GENIChomozygous986140772
137025888170258882GA22GENIChomozygous986140773