chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
168167646816765TG52GENICpossibly homozygous60612545
168170036817004A-25GENIChomozygous60612546
168172766817277AAG39GENIChomozygous60612547
168176746817675TG49GENIChomozygous60612548
168183786818379GC51GENICpossibly homozygous60612549