chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1242322324232233TC20GENIChomozygous668714182
1242327264232727AG2GENIChomozygous668714183
1242328904232891TTCCCTCC1GENIChomozygous768229964
1242338354233836GC22GENICpossibly homozygous668714184
1242338884233889GA17GENICpossibly homozygous668714185
1242340884234089TC16GENICheterozygous668714186
1242343054234306TC12GENIChomozygous668714187
1242344524234453TC4GENIChomozygous668714188
1242350874235088TG15GENICpossibly homozygous668714189
1242355454235546GC12GENIChomozygous668714190
1242358524235853CA15GENICpossibly homozygous668714191
1242359274235928TC14GENIChomozygous668714192
1242359854235986TC10GENIChomozygous668714193
1242373164237317GT17GENIChomozygous668714194
1242374124237413TTGGTTATTCAACTCGACCTTTGAA3GENICheterozygous768229967
1242374454237446AAT2GENIChomozygous768229968
1242374524237453GA9GENIChomozygous668714195
1242396454239646TA15GENICpossibly homozygous668714196
1242401504240151CCT4GENICheterozygous768229969
1242420704242071T-22GENICpossibly homozygous768229970
1242455704245571TTAC3GENICheterozygous768229973
1242472674247268AT10GENICheterozygous668714197
1242519794251980AG5GENIChomozygous668714198
1242547014254709TACATACA--------1GENIChomozygous768229974
1242555614255562CT11GENICpossibly homozygous668714199
1242590844259085GA12GENICpossibly homozygous668714200