chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18034168980341690CT51GENICpossibly homozygous142835375
18034189680341897TA52GENIChomozygous142835376
18034207880342079CT46GENIChomozygous142835377
18034300880343009AG48GENIChomozygous142835378
18034366680343667CT48GENIChomozygous142835379
18034369380343694TC48GENIChomozygous142835380
18034858280348583AG45GENIChomozygous142835381
18035809080358091GA46GENIChomozygous142835382
18035979180359791CCTCC18GENIChomozygous142788753
18035965080359651C47GENIChomozygous142788752
18035322180353222GA15GENICheterozygous403699447
18035322180353222G15GENIChomozygous403699446