chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
67556197775561978TC16GENIChomozygous114861553
67556340775563408AC19GENIChomozygous114861555
67556422375564224AG18GENIChomozygous114861556
67556557175565572CG16GENIChomozygous115124978
67556597475565975CT29GENIChomozygous115124979
67556610575566106GC19GENIChomozygous114861557
67557215375572154GA22GENIChomozygous114861560
67557297275572973AG17GENIChomozygous114861561
67557347475573475GA18GENIChomozygous115124987
67557462375574624AG16GENIChomozygous114861563
67557606975576070AG10GENIChomozygous114861564
67557673775576738GA6GENIChomozygous114861565
67557871275578713CT27GENIChomozygous115124990
67557899675578997TC26GENIChomozygous114861567
67557909175579092GA31GENIChomozygous115124991
67557912375579124GC31GENIChomozygous114861568
67558425075584251AT7GENICpossibly homozygous115258006
67558708375587084AC36GENIChomozygous114861577
67558813975588140AT16GENIChomozygous115125002