chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4168397330168397331GA21GENIChomozygous113475588
4168399526168399527AG23GENIChomozygous112943834
4168399971168399972AG23GENIChomozygous112943836
4168401606168401607AT22GENIChomozygous113475590
4168405540168405541AG18GENIChomozygous112943853
4168407795168407796AG26GENIChomozygous112943867
4168410973168410974CT19GENIChomozygous113475592
4168413143168413144CT24GENIChomozygous113475594
4168420622168420623GC33GENIChomozygous112943925
4168423565168423566GT21GENICheterozygous113475596
4168423798168423799AG12GENIChomozygous113475598
4168429330168429331GA19GENIChomozygous113475600
4168429698168429699GA23GENIChomozygous112943933
4168424684168424685GA3GENICheterozygous119348906
4168433053168433054CG10GENIChomozygous113475602
4168433645168433646GA18GENIChomozygous113475604
4168443797168443798CG26GENIChomozygous112943947
4168449952168449953CT11GENIChomozygous113475606
4168450005168450006CT15GENIChomozygous113475608
4168453960168453961TA22GENIChomozygous113475610
4168454070168454071CT16GENIChomozygous112943953
4168457521168457522AG23GENIChomozygous112943955
4168459208168459209GA15GENIChomozygous113475612
4168461092168461093GT16GENIChomozygous113475614
4168461104168461105GA14GENIChomozygous113475616
4168461194168461195AG4GENIChomozygous113475618
4168462072168462073GA14GENIChomozygous113475620
4168462148168462149AG17GENIChomozygous113475622
4168465309168465310GA20GENIChomozygous112943988