chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144163972144163973CT20GENIChomozygous114036704
5144164594144164595TG24GENIChomozygous114253951
5144167500144167501CG22GENIChomozygous114253953
5144167565144167566TC33GENIChomozygous114036706
5144169769144169770AT42GENICpossibly homozygous114253955
5144169921144169922TC48GENIChomozygous114036707
5144169938144169939AG45GENIChomozygous114036708
5144170147144170148GA32GENIChomozygous119085354
5144171171144171172AG33GENIChomozygous114036709
5144172133144172134GA26GENIChomozygous114253957
5144172935144172936CT33GENIChomozygous114253959
5144175239144175240GT32GENIChomozygous114036712
5144177554144177555GT20GENIChomozygous119085355
5144173685144173686CA26GENIChomozygous118846232