chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8121844635121844636TC21GENIChomozygous567310932
8121845622121845623TC3GENIChomozygous567310933
8121845798121845799GC5GENIChomozygous567310934
8121847010121847011AG20GENIChomozygous567310935
8121847014121847015CT19GENIChomozygous567310936
8121847292121847293AAC22GENICpossibly homozygous710462926
8121847294121847295AAAC22GENICpossibly homozygous710462927
8121847499121847500GGAC11GENIChomozygous710462928
8121848033121848043AAAAAAAAAA----------5GENICheterozygous710462929
8121848289121848290GGA5GENIChomozygous710462930