chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123925353539253536TG2GENIChomozygous964847914
123925356539253566GC2GENIChomozygous964847915
123925363539253636GA2GENIChomozygous964847916
123925363639253637AG2GENIChomozygous964847917
123925366139253662AG2GENIChomozygous964847918
123927405139274052AG17GENICpossibly homozygous964847919
123927416139274162GT25GENIChomozygous964847920
123927451439274515AG31GENIChomozygous964847921
123927453139274532AC30GENIChomozygous964847922
123927668639276687CA20GENIChomozygous964847923
123927668739276688TG20GENIChomozygous964847924
123927726139277262TG21GENIChomozygous964847925
123927726239277263GT21GENIChomozygous964847926
123927738139277382GC35GENIChomozygous964847927