chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101460452014604521GT21GENIChomozygous138726281
101460453114604532GA19GENIChomozygous138726282
101460453714604538GA19GENIChomozygous138726283
101460453714604538G19GENICheterozygous403277042
101460453914604540GA18GENIChomozygous138726284
101460453914604540G18GENICheterozygous403277043
101460454014604541GA17GENIChomozygous138726285
101460454014604541G17GENICheterozygous403277044
101460560014605601C57GENIChomozygous138669144
101460461314604614G21GENIChomozygous138669140
101460542614605426A30GENIChomozygous138669142
101460548414605485G31GENIChomozygous138669143
101460880914608809T75GENIChomozygous138669145
101460883614608837C73GENIChomozygous138669146
101460912414609124G63GENIChomozygous138669147
101461122314611223C51GENIChomozygous138669148
101461141314611413T55GENIChomozygous138669149
101461161614611616T57GENIChomozygous138669150
101461163214611632T53GENIChomozygous138669151
101461353414613535G59GENIChomozygous138669152
101461355914613560G54GENIChomozygous138669153
101461437514614375T46GENIChomozygous138669154
101461440114614402C45GENIChomozygous138669155
101461447714614478G46GENIChomozygous138669156
101461458414614584C57GENIChomozygous138669157
101461461114614612A62GENIChomozygous138669158
101461632714616328T51GENIChomozygous138669160
101461674414616744G62GENIChomozygous138669161
101461687114616871C57GENIChomozygous138669162
101461689914616899G57GENIChomozygous138669163
101466356714663568CT3GENIChomozygous144859482