chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174566920745669208TC27GENIChomozygous787358195
174566922045669221GC28GENIChomozygous787358196
174567129545671296AC44GENIChomozygous787358197
174567334645673347TA20GENIChomozygous787358198
174567379945673800AG18GENIChomozygous787358199
174567548545675486TC26GENIChomozygous787358200
174567576545675766TC20GENICpossibly homozygous787358201
174567694745676948TA19GENIChomozygous787358202
174567816545678166AG29GENIChomozygous787358203
174567910545679106GT10GENIChomozygous787358204
174567946545679466TC26GENIChomozygous787358205
174567953445679535GC26GENIChomozygous787358206