chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105649310356493104GT52GENIChomozygous116783612
105649312756493128AG56GENIChomozygous116783614
105649877256498773AG51GENIChomozygous116783618
105649921956499220GA64GENIChomozygous116783620
105649969156499692CG47GENIChomozygous116935391
105650154556501546TA10GENIChomozygous116978068
105650317456503175AG56GENIChomozygous116783624
105650334156503342AG56GENIChomozygous116935393
105650396756503968TC48GENICpossibly homozygous116783626
105650547856505479TC41GENIChomozygous116935395
105650605156506052GC50GENICpossibly homozygous116783630
105650617856506179CT59GENICpossibly homozygous116783632