chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7125746090125746091CT34GENICpossibly homozygous656666840
7125747342125747343CT25GENIChomozygous656666841
7125747534125747535CT29GENIChomozygous656666842
7125747571125747572GA36GENIChomozygous656666843
7125748329125748330AG37GENIChomozygous656666844
7125748927125748928GA37GENIChomozygous656666845
7125749012125749013GA34GENIChomozygous656666846
7125749414125749415AG27GENIChomozygous656666847
7125751521125751522AATT12GENIChomozygous761024541
7125752000125752001TC24GENICpossibly homozygous656666848
7125752756125752757GA24GENIChomozygous656666849
7125753821125753822CT29GENIChomozygous656666850
7125753897125753898CT27GENIChomozygous656666851
7125753949125753950GA30GENIChomozygous656666852
7125754274125754275AG18GENIChomozygous656666853
7125754320125754321CT28GENIChomozygous656666854
7125754367125754368CT33GENIChomozygous656666855
7125754379125754380GC33GENIChomozygous656666856
7125755157125755158GA22GENIChomozygous656666857
7125755666125755667CT42GENICpossibly homozygous656666858
7125755703125755704CT38GENIChomozygous656666859
7125756500125756501TC18GENIChomozygous656666860
7125756849125756850AG21GENIChomozygous656666861
7125756965125756966GGAAAA7GENICpossibly homozygous761024543
7125756965125756966GGAAAAAAAAAAA7GENICheterozygous761024544
7125757153125757154TTA21GENIChomozygous761024545