chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1157403890157403891AC35GENICpossibly homozygous108325665
1157405189157405190TA9GENIChomozygous108325674
1157406741157406742AC20GENIChomozygous108325676
1157407469157407470GT15GENIChomozygous108325678
1157408452157408453TC9GENIChomozygous108325680
1157409776157409777AG19GENIChomozygous108325682
1157413967157413968GT8GENIChomozygous108325684