chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
72478829324788294CA19GENIChomozygous53838864
72478907724789078T-19GENIChomozygous53838865
72478982924789830TTA17GENIChomozygous53838866
72479047824790479TTCACACACACACA4GENICheterozygous54961639
72479047824790479TTCACACACACA4GENICheterozygous55021792
72479158924791590AG24GENIChomozygous53838867
72479339424793395TC25GENIChomozygous53838868
72479367324793674TTC34GENIChomozygous53838869
72479375724793758GA27GENIChomozygous53838870
72479423524794236CT23GENIChomozygous53838871
72479435924794360GGA20GENICpossibly homozygous53838872
72479501624795017G-15GENIChomozygous53838873
72479505824795059AG24GENIChomozygous53838874
72479512424795125G-25GENIChomozygous53838875
72479521124795212AAC16GENIChomozygous53838876
72479524124795242TTC12GENIChomozygous53838877
72479550324795504AG23GENIChomozygous53838886
72479686524796866GGA8GENICheterozygous55021793
72479758724797588TC37GENIChomozygous53838887