chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6101055537101055538GGCC15GENIChomozygous55524181
6101055554101055556GC--21GENIChomozygous55419821
6101056135101056136CCTTT5GENICheterozygous55524183
6101055958101055962ACAG----14GENIChomozygous54601814
6101056135101056136CCTTTT5GENICheterozygous54601815
6101056561101056562AG20GENIChomozygous54601818
6101056889101056890T-22GENIChomozygous54601820
6101057505101057506GA24GENIChomozygous54601821
6101058413101058414A-12GENIChomozygous54601822
6101058901101058902TG3GENIChomozygous54601824
6101058958101058959TTGAG11GENIChomozygous54601825
6101059518101059519AG26GENIChomozygous54601826
6101059884101059885AG28GENIChomozygous54601827
6101060936101060937CCT11GENICpossibly homozygous54601828
6101061380101061381GA8GENIChomozygous54601830
6101062368101062369AAT14GENIChomozygous54601831
6101062423101062435GCACACCTCAGC------------13GENIChomozygous54601832
6101062947101062948TA13GENIChomozygous54601833
6101064349101064350TA19GENIChomozygous54601834
6101065477101065478TTACCTGAAAAA22GENIChomozygous54601836
6101066118101066119GGT21GENIChomozygous54601837
6101066831101066832AG17GENIChomozygous54601838
6101067142101067143CT12GENIChomozygous54601839
6101067165101067166GA11GENIChomozygous54601840
6101067168101067169GC11GENIChomozygous54601841
6101067169101067170GC11GENIChomozygous54601842
6101067296101067297AC11GENIChomozygous54601846
6101067419101067426TTTTTTT-------1GENIChomozygous54601848
6101061885101061891TTTGTT------5GENICheterozygous55524189