chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142293282322932824GA75GENIChomozygous782141041
142293447722934478TC22GENIChomozygous782141042
142293448022934481AC23GENIChomozygous782141043
142293451722934518TC39GENIChomozygous782141044
142293494122934942CA55GENICheterozygous782141045
142293494922934950TC51GENICheterozygous782141046
142293498322934984TC71GENICheterozygous782141047
142293498422934985GA70GENICheterozygous782141048
142293499922935000CG75GENICheterozygous782141049
142293764622937647TA60GENIChomozygous782141050
142294094922940950AG69GENIChomozygous782141051
142294134322941344CA53GENIChomozygous782141052
142294277722942778CA26GENIChomozygous782141053
142294389522943896AG63GENIChomozygous782141054
142294402922944030TA71GENICpossibly homozygous782141055
142294751922947520CA66GENIChomozygous782141056
142294752122947522AC65GENICpossibly homozygous782141057
142294826322948264CA27GENIChomozygous782141058
142294884322948844GA53GENICpossibly homozygous782141059
142295072522950726AT47GENICheterozygous782141060
142295235922952360CG53GENIChomozygous782141061
142295489422954895GA24GENICheterozygous782141062
142295552222955523CT65GENIChomozygous782141063
142295557922955580GT60GENIChomozygous782141064