chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
161070513010705131AG24GENIChomozygous566832135
161070820810708209T-13GENICpossibly homozygous709212148
161071168810711689AG21GENIChomozygous566832136
161071211010712112GT--12GENICheterozygous709212151
161071365410713655CT21GENIChomozygous567774577
161071616010716161CT20GENIChomozygous566832137
161071898410718985C-26GENIChomozygous709212153
161071902010719021AT19GENIChomozygous567774578
161071905610719058CC--3GENIChomozygous709212154
161072195710721958AG16GENIChomozygous566832138
161072413510724136GGCCCC3GENIChomozygous709212155
161072553210725533AG21GENIChomozygous566832139
161073131710731332TTCTTTTCTTTTCTT---------------2GENIChomozygous709212157
161073280110732802GT18GENIChomozygous566832140
161073280210732803CA18GENIChomozygous566832141
161073310110733102CA32GENIChomozygous566832142
161073338010733381TC37GENIChomozygous566832143
161073567510735676TTCAGGGGC2GENIChomozygous709212160
161073582310735824AG1GENIChomozygous566832144
161074541310745414AG30GENIChomozygous566832145
161074650810746509TTTGCCAGGCAAGCG1GENIChomozygous709212161
161074651210746513TTACCACTGAGCTAAA1GENIChomozygous709212162
161075243610752437TC20GENIChomozygous566832146
161075301710753018TC22GENIChomozygous566832147
161075466610754667GGACAC4GENICheterozygous709212163
161075466610754667GGACACAC4GENICheterozygous709212164
161075975210759753TC12GENIChomozygous566832148
161076253410762535TA30GENIChomozygous567774579
161076759910767605GTGTGT------5GENICheterozygous709212168
161076901210769013CT12GENIChomozygous566832149