chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
72478829324788294CA22GENIChomozygous53838864
72478907724789078T-29GENIChomozygous53838865
72478982924789830TTA30GENICpossibly homozygous53838866
72479047824790479TTCACACACACACA11GENICheterozygous54961639
72479047824790479TTCACACACACA11GENICheterozygous55021792
72479158924791590AG36GENIChomozygous53838867
72479339424793395TC22GENIChomozygous53838868
72479367324793674TTC34GENIChomozygous53838869
72479375724793758GA27GENIChomozygous53838870
72479423524794236CT32GENIChomozygous53838871
72479435924794360GGA30GENIChomozygous53838872
72479501624795017G-32GENIChomozygous53838873
72479505824795059AG27GENIChomozygous53838874
72479512424795125G-19GENIChomozygous53838875
72479521124795212AAC19GENIChomozygous53838876
72479524124795242TTC20GENIChomozygous53838877
72479550324795504AG19GENIChomozygous53838886
72479758724797588TC43GENIChomozygous53838887