chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85998174559981746TG40GENIChomozygous52665814
85998182959981830AG37GENIChomozygous52665816
85998423759984238TG20GENIChomozygous52665818
85998426059984261CT24GENIChomozygous52665820
85998442859984430AC--9GENIChomozygous52665824
85998495859984959AG26GENIChomozygous52665826
85998497359984974CT21GENIChomozygous52665828
85998502459985025AG29GENIChomozygous52665830
85998503959985040TC36GENIChomozygous52665832
85998562059985621GA27GENIChomozygous52665834
85998573859985739AG16GENIChomozygous52665836
85998598759985989GC--28GENIChomozygous52665838
85998609659986097TC32GENIChomozygous52665842
85998701459987015TC33GENICpossibly homozygous52665844
85998706159987062CG37GENIChomozygous52665846
85998724259987243TC22GENIChomozygous52665848
85998987459989875AC20GENIChomozygous52665850
85999000959990011GA--21GENIChomozygous52665852
85999047959990481GT--18GENIChomozygous52665854
85999048859990489GC23GENIChomozygous52665856
85999176959991770TC34GENIChomozygous52665858
85999201159992012AG20GENIChomozygous52665860
85999207559992076AT25GENIChomozygous52665862
85999260759992608CCG24GENIChomozygous52665864
85999311359993114CT23GENIChomozygous52665866
85999358459993585GA42GENIChomozygous52665868
85999365059993651TTC18GENIChomozygous52665870
85999393659993937A-25GENIChomozygous52665872
85999401559994016GT21GENIChomozygous52665875
85999412059994121TG20GENIChomozygous52665877
85999419059994191CT22GENIChomozygous52665879
85999459359994594AT24GENIChomozygous52665881
85999465559994656GA15GENIChomozygous52665883
85999501359995014GA28GENIChomozygous52665885