chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157791822157791823TC34GENIChomozygous112907272
4157791833157791834TC30GENICpossibly homozygous112907274
4157791845157791846TA38GENICpossibly homozygous112907276
4157791851157791852TC39GENICpossibly homozygous112907278
4157791863157791864AT41GENICheterozygous112907280
4157792271157792272GA49GENIChomozygous112907282
4157793017157793018GT59GENICpossibly homozygous112907284
4157795166157795167CT27GENIChomozygous112907286
4157796662157796663TC54GENIChomozygous112907288
4157796750157796751CT36GENIChomozygous112907290
4157797124157797125GA55GENIChomozygous112907292
4157797798157797799GT23GENICheterozygous112907294
4157797801157797802CT23GENICheterozygous112907296
4157797854157797855TG31GENIChomozygous112907298
4157798356157798357TG56GENIChomozygous112907300