chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
36785006467850065CT31GENIChomozygous112341780
36785092367850924GA20GENIChomozygous111598636
36785125767851258AT22GENIChomozygous112341781
36785137867851379TC27GENIChomozygous111598639
36785145267851453GA33GENIChomozygous111598640
36785207267852073TC30GENIChomozygous111598642
36785225067852251AG15GENIChomozygous112341782
36785246767852468CT22GENIChomozygous111598643
36785259567852596GA16GENIChomozygous111598644
36785269867852699CT27GENIChomozygous111598645
36785314067853141GT22GENIChomozygous112341783
36785345567853456AG16GENIChomozygous111598646
36785370167853702GA25GENIChomozygous112341784
36785377567853776CT35GENIChomozygous111598647
36785442667854427AG32GENIChomozygous111598648
36785452467854525CT42GENIChomozygous111598649
36785457167854572AT46GENIChomozygous111598650
36785504767855048GA33GENIChomozygous111598651
36785558067855581CT24GENIChomozygous112341785
36785568067855681CT24GENIChomozygous112341786
36785605667856057GA22GENIChomozygous112341787
36785620267856203GC33GENIChomozygous111598653
36785750467857505AG15GENIChomozygous112341790
36785823167858232CG25GENIChomozygous119649822
36785846667858467CT38GENIChomozygous112341791
36785974067859741TA31GENICpossibly homozygous119649823
36785974167859742AG32GENICpossibly homozygous119649824
36786024267860243GA24GENIChomozygous112341792
36786039667860397CT21GENIChomozygous111598660
36786070567860706AG16GENIChomozygous111598661
36786076267860763AG22GENIChomozygous111598662
36786110867861109GA21GENIChomozygous112341793
36786155167861552AG24GENIChomozygous111598663
36786212367862124GA19GENIChomozygous111598665