chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1157403862157403863TC19GENICheterozygous108325661
1157403890157403891AC18GENICpossibly homozygous108325665
1157405189157405190TA26GENIChomozygous108325674
1157406741157406742AC21GENIChomozygous108325676
1157407469157407470GT39GENIChomozygous108325678
1157408452157408453TC32GENIChomozygous108325680
1157413967157413968GT32GENIChomozygous108325684