chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
168167646816765TG12GENIChomozygous60612545
168170036817004A-11GENIChomozygous60612546
168172196817220CT19GENICpossibly homozygous61840587
168172766817277AAG16GENIChomozygous60612547
168176746817675TG18GENIChomozygous60612548
168183786818379GC8GENICpossibly homozygous60612549