chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1204836591204836592GA15GENIChomozygous75735700
1204836991204836992AG15GENIChomozygous75735701
1204837439204837440AG17GENIChomozygous75735702
1204837861204837862TC21GENIChomozygous75735703
1204839356204839357CA24GENIChomozygous75735704
1204841314204841315GA11GENIChomozygous75735705
1204842068204842069GA19GENICpossibly homozygous75735706
1204842698204842699GA18GENIChomozygous75735707
1204838881204838882CA19GENIChomozygous75877675
1204838892204838893AG18GENIChomozygous74678285
1204842984204842985GA20GENIChomozygous74678289
1204843595204843596TC11GENIChomozygous74678291
1204845150204845151TC17GENIChomozygous74678293
1204845891204845892AG27GENIChomozygous74678295
1204846036204846037TG19GENIChomozygous74678297
1204846351204846352GA23GENIChomozygous74678299
1204846745204846746GA27GENIChomozygous74678301
1204847776204847777GA26GENIChomozygous75735708
1204848500204848501TC21GENIChomozygous74678303
1204849200204849201GA30GENIChomozygous74678307
1204853989204853990GA23GENIChomozygous75735709