chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
114245168042451681GC35GENICheterozygous518072081
114245171542451716AC48GENICheterozygous518072082
114245172042451721GT52GENICheterozygous518072083
114245172242451723GC53GENICheterozygous518072084
114245172442451725GA56GENICheterozygous518072085
114245173642451737CT68GENICheterozygous518072086
114245175542451756GA88GENICheterozygous518072087
114245177442451775GA85GENICheterozygous518072088
114245181142451812GC115GENICheterozygous518072089
114245186442451865TG102GENICheterozygous518072090
114245190242451903GA66GENICheterozygous518072091
114245190942451910AC64GENICheterozygous518072092
114245193142451932TC65GENICheterozygous518072093
114245200842452009CG51GENICheterozygous518072094
114245201142452012TC48GENICheterozygous518072095
114245205942452060CG48GENICheterozygous518072096
114245211842452119CT25GENICheterozygous518072097
114245214342452144AG11GENICpossibly homozygous518072098
114245215542452156CT12GENICheterozygous518072099
114245260842452609TTAGAG4GENIChomozygous689559059
114245282942452830TC8GENIChomozygous518072100
114245287042452871GA11GENICheterozygous518072101
114245288442452885GA9GENIChomozygous518072102
114245308942453090AG34GENIChomozygous518072103