chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
72478829324788294CA17GENIChomozygous53838864
72478907724789078T-18GENIChomozygous53838865
72478982924789830TTA20GENIChomozygous53838866
72479047824790479TTCACACACA6GENICheterozygous54961637
72479047824790479TTCACACACACACA6GENICheterozygous54961639
72479158924791590AG17GENIChomozygous53838867
72479339424793395TC39GENIChomozygous53838868
72479367324793674TTC35GENIChomozygous53838869
72479375724793758GA40GENIChomozygous53838870
72479423524794236CT22GENIChomozygous53838871
72479435924794360GGA21GENICpossibly homozygous53838872
72479501624795017G-19GENIChomozygous53838873
72479505824795059AG27GENIChomozygous53838874
72479512424795125G-33GENIChomozygous53838875
72479521124795212AAC22GENIChomozygous53838876
72479524124795242TTC17GENIChomozygous53838877
72479550324795504AG24GENIChomozygous53838886
72479758724797588TC25GENIChomozygous53838887