chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151141452151141453AG24GENIChomozygous55795526
5151142387151142388TA17GENIChomozygous55795527
5151145022151145023CT39GENIChomozygous55795528
5151145762151145763CT32GENIChomozygous55795529
5151149034151149035CT32GENIChomozygous55795530
5151149723151149724TG27GENIChomozygous55795531
5151150210151150211AACT31GENIChomozygous55795532
5151150626151150627AC34GENIChomozygous55795533
5151152138151152139TTGG8GENIChomozygous55795534
5151152452151152453TC25GENIChomozygous55795535
5151152584151152585AG31GENIChomozygous55795536
5151153256151153257AAG5GENICheterozygous55795544
5151153274151153275GGAGAGAA16GENIChomozygous55795546
5151153558151153559AG41GENIChomozygous55795547
5151153687151153688AG40GENIChomozygous55795548
5151154015151154016TA11GENICpossibly homozygous55795549
5151154017151154018TA12GENICpossibly homozygous55795550
5151154122151154123GA24GENIChomozygous55795552
5151154262151154263A-24GENIChomozygous55795553
5151154274151154275GA26GENIChomozygous55795554
5151154800151154801GA29GENIChomozygous55795555
5151154993151154994AT28GENIChomozygous55795556
5151155338151155339AG18GENIChomozygous55795557
5151155431151155432CT27GENIChomozygous55795558
5151155555151155556GC28GENIChomozygous55795559
5151156199151156200AG38GENIChomozygous55795560
5151156329151156330GT25GENIChomozygous55795561
5151156797151156798GC21GENIChomozygous55795562
5151156923151156924TC13GENIChomozygous55795563
5151157760151157761GA37GENIChomozygous55795564
5151157830151157831CT18GENIChomozygous55795565
5151154048151154062CGCGCGCGCGCGCG--------------4GENICheterozygous56532733