chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4102725070102725071GA20GENIChomozygous137184532
4102725949102725950AT17GENIChomozygous137184533
4102726581102726581AGAC8GENICheterozygous143057709
4102726582102726583TC8GENICheterozygous137184535
4102730985102730986GA14GENIChomozygous137184536
4102739195102739196TA22GENICpossibly homozygous137184537
4102744204102744205CA12GENIChomozygous137184538
4102747754102747755GA18GENIChomozygous137184539
4102733040102733041GA17GENIChomozygous143134963
4102727623102727623TCCA19GENIChomozygous136908586
4102739305102739305A13GENICheterozygous136908587