chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
151933902519339026CT9GENIChomozygous112662209
151933982319339824TG17GENICpossibly homozygous112465852
151934078819340789GA6GENIChomozygous112465854
151934136019341361TC13GENIChomozygous112465858
151934193819341939GA20GENIChomozygous112465860
151934374319343744GA16GENIChomozygous112662211
151934522519345226GA20GENIChomozygous112465862
151934540619345407TC16GENIChomozygous112465864
151934546319345464GA17GENIChomozygous112465866
151934639719346398CT28GENIChomozygous112465868
151934643619346437CT34GENIChomozygous112465870
151934649719346498TC35GENIChomozygous112465872
151934693319346934GA16GENIChomozygous112465874
151934728119347282GA21GENIChomozygous112465876
151934736519347366CT17GENIChomozygous112465878
151934750019347501CT17GENIChomozygous112465880
151934754719347548CA15GENIChomozygous112465882
151934768219347683TG28GENIChomozygous112465884
151934790019347901TC28GENIChomozygous112465886
151934801319348014GA30GENIChomozygous112465888
151934801519348016GA30GENIChomozygous112465890
151934829219348293CT29GENIChomozygous112465892
151934836219348363AG24GENIChomozygous112465894
151934845919348460GA22GENIChomozygous112465896
151934847419348475TC22GENIChomozygous112465898
151934887719348878GA27GENIChomozygous112465900