chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151141452151141453AG17GENIChomozygous55795526
5151142387151142388TA7GENIChomozygous55795527
5151145022151145023CT22GENICpossibly homozygous55795528
5151145762151145763CT24GENICpossibly homozygous55795529
5151148817151148818A-5GENICheterozygous56591495
5151149034151149035CT22GENIChomozygous55795530
5151149723151149724TG19GENIChomozygous55795531
5151150210151150211AACT6GENICheterozygous55795532
5151150626151150627AC14GENICpossibly homozygous55795533
5151152452151152453TC27GENICpossibly homozygous55795535
5151152584151152585AG17GENIChomozygous55795536
5151153274151153275GGAGAGAA4GENIChomozygous55795546
5151153558151153559AG18GENICpossibly homozygous55795547
5151153687151153688AG23GENICpossibly homozygous55795548
5151154122151154123GA17GENIChomozygous55795552
5151154262151154263A-3GENIChomozygous55795553
5151154274151154275GA5GENICheterozygous55795554
5151154800151154801GA32GENIChomozygous55795555
5151154993151154994AT27GENICpossibly homozygous55795556
5151155338151155339AG3GENIChomozygous55795557
5151155431151155432CT17GENICheterozygous55795558
5151155555151155556GC26GENICpossibly homozygous55795559
5151156199151156200AG17GENICpossibly homozygous55795560
5151156329151156330GT26GENICpossibly homozygous55795561
5151156797151156798GC18GENICpossibly homozygous55795562
5151156923151156924TC4GENICheterozygous55795563
5151157760151157761GA19GENICpossibly homozygous55795564
5151157830151157831CT4GENICheterozygous55795565