chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108998088789980888GC4GENICheterozygous128873484
108998095389980954GT7GENICpossibly homozygous128873485
108998095489980955CT7GENICpossibly homozygous128873486
108998112389981124CG2GENIChomozygous128873487
108998112489981125TC2GENIChomozygous128873488
108998369389983694AT16GENICheterozygous130397765
108998400989984010GC16GENICheterozygous128873495
108998401489984015TC15GENICheterozygous123455745
108998409589984096GA25GENICheterozygous130397766
108998429589984296GC29GENICheterozygous118007666
108998431189984312TC32GENICheterozygous130397767
108998455389984554CT36GENICheterozygous130397768
108998455889984559GA38GENICheterozygous118007667
108998464189984642GC23GENICheterozygous118049056
108998464289984643GA23GENICheterozygous118049057
108998466089984661CT23GENICheterozygous118007668
108998474189984742GA28GENICheterozygous130397769
108998474989984750CT26GENICheterozygous130397770
108998481389984815CA25GENICheterozygous130394203
108998489189984892GC24GENICheterozygous118007669
108998495989984960CT22GENICheterozygous130397771
108998505089985051GT22GENICheterozygous118007670