chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3151565213151565214AG32GENICpossibly homozygous111777718
3151566594151566595GA24GENIChomozygous112310773
3151567986151567987CT26GENIChomozygous111777720
3151569189151569190TC32GENIChomozygous111777722
3151569216151569217GA35GENICpossibly homozygous112310775
3151569564151569565CA27GENICpossibly homozygous112310777
3151569833151569834TC48GENIChomozygous111777724
3151569893151569894AG42GENIChomozygous111777726
3151570874151570875TC34GENIChomozygous111777728
3151571723151571724CT26GENICheterozygous112310779
3151573651151573652CT25GENIChomozygous111777730
3151575803151575804GA42GENIChomozygous112310781
3151580014151580015GA29GENICpossibly homozygous111777736
3151580053151580054CT27GENICpossibly homozygous111777738
3151580079151580080GA51GENICheterozygous111777740
3151580129151580130GA68GENICheterozygous112310783
3151581224151581225AC37GENIChomozygous111777742
3151583542151583543TA26GENIChomozygous112310785