chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113750099337500994CT7GENICpossibly homozygous50736729
113750104137501042TC15GENICpossibly homozygous50736730
113750165937501660AAAGT1GENIChomozygous50736733
113750324237503243T-1GENIChomozygous50736738
113750585337505854AT24GENICpossibly homozygous50736742
113750643237506433AG24GENIChomozygous50736743
113750645837506459GA20GENICpossibly homozygous50736744
113750796437507965AAT6GENICheterozygous50736746
113750886837508869CT18GENIChomozygous50736747