chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101460452014604521GT10GENIChomozygous138726281
101460453114604532GA9GENIChomozygous138726282
101460453714604538GA8GENIChomozygous138726283
101460453714604538G8GENICheterozygous403277042
101460453914604540GA8GENIChomozygous138726284
101460453914604540G8GENICheterozygous403277043
101460454014604541GA8GENIChomozygous138726285
101460454014604541G8GENICheterozygous403277044
101460560014605601C13GENIChomozygous138669144
101460461314604614G8GENIChomozygous138669140
101460542614605426A28GENICpossibly homozygous138669142
101460548414605485G29GENIChomozygous138669143
101460880914608809T12GENIChomozygous138669145
101461141314611413T17GENIChomozygous138669149
101460883614608837C10GENIChomozygous138669146
101460912414609124G27GENIChomozygous138669147
101461122314611223C21GENIChomozygous138669148
101461161614611616T26GENIChomozygous138669150
101461163214611632T28GENIChomozygous138669151
101461353414613535G16GENIChomozygous138669152
101461355914613560G14GENIChomozygous138669153
101461437514614375T20GENIChomozygous138669154
101461440114614402C20GENIChomozygous138669155
101461447714614478G17GENIChomozygous138669156
101461458414614584C14GENIChomozygous138669157
101461461114614612A13GENIChomozygous138669158
101461632714616328T18GENIChomozygous138669160
101461674414616744G16GENIChomozygous138669161
101461687114616871C18GENIChomozygous138669162
101461689914616899G17GENIChomozygous138669163