chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157791822157791823TC27GENIChomozygous793723468
4157791833157791834TC23GENIChomozygous793723469
4157791845157791846TA22GENICpossibly homozygous793723470
4157791851157791852TC25GENICheterozygous793723471
4157791863157791864AT25GENICheterozygous793723472
4157792271157792272GA30GENIChomozygous793723473
4157793017157793018GT28GENICpossibly homozygous793723474
4157795166157795167CT27GENIChomozygous793723475
4157796662157796663TC20GENIChomozygous793723476
4157796750157796751CT25GENIChomozygous793723477
4157797124157797125GA39GENIChomozygous793723478
4157797798157797799GT23GENICheterozygous793723479
4157797801157797802CT23GENICheterozygous793723480
4157797854157797855TG25GENICpossibly homozygous793723481
4157798356157798357TG29GENIChomozygous793723482