chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102955936729559368GA49GENICpossibly homozygous68349018
102955944829559449TC45GENIChomozygous67835641
102955956229559563AG35GENIChomozygous67835645
102956035029560351GA41GENIChomozygous68349020
102956089429560895CT36GENIChomozygous67835657
102956095329560954CT30GENIChomozygous67835665
102956095829560959AG31GENIChomozygous67835668
102956183829561839CT24GENIChomozygous68349022
102956195629561957TA23GENIChomozygous68349024
102956218729562188AG44GENIChomozygous67835686
102956222429562225AT33GENIChomozygous68349026
102956254829562549TG38GENIChomozygous68349029
102956255829562559CT33GENIChomozygous68349031
102956302629563027GA21GENIChomozygous68349033
102956305429563055TG22GENIChomozygous67835704
102956339829563399TC27GENIChomozygous67835708
102956341629563417CT31GENIChomozygous68349037
102956367529563676AG29GENIChomozygous67835713
102956368329563684GA22GENIChomozygous68349039
102956410029564101CT24GENICheterozygous68349043
102956469929564700CT28GENIChomozygous68349045
102956548429565485CT43GENIChomozygous68349047
102956639529566396GA52GENIChomozygous67835729
102956664829566649GT39GENIChomozygous67835733
102956719729567198AG43GENIChomozygous67835737
102956748929567490AG35GENICheterozygous68349049
102956760229567603CT30GENIChomozygous67835745
102956768229567683TC34GENIChomozygous67835749
102956810629568107GA26GENIChomozygous67835754
102956814129568142GC30GENIChomozygous67835758