chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1100615343100615344TA16GENIChomozygous108164980
1100632053100632054AG4GENIChomozygous108164981
1100634209100634209GGTG25GENIChomozygous127408660
1100634212100634216AACA23GENIChomozygous127408661
1100634267100634268C19GENIChomozygous127408662
1100641846100641847G5GENICheterozygous130210957
1100645153100645154AG11GENICpossibly homozygous108164984
1100646965100646966TG17GENIChomozygous108164985
1100668636100668637GA17GENICheterozygous133466675
1100668981100668982T16GENIChomozygous127408664