chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41732445217324453GA18GENIChomozygous112527620
41732492817324929GA24GENICpossibly homozygous112527622
41732512017325121AC29GENIChomozygous112527624
41732523717325238AG33GENIChomozygous112527626
41732546317325464GA26GENIChomozygous112527628
41732555517325556AT31GENIChomozygous112527630
41732586317325864AC26GENIChomozygous112527632
41732589217325893TC24GENIChomozygous112527634
41732593517325936AG25GENIChomozygous112527636
41732596617325967CT24GENIChomozygous112527638
41732625117326252CT22GENIChomozygous112527640
41732628617326287TC28GENIChomozygous112527642
41732638117326382TC26GENIChomozygous112527644
41732644417326445CA28GENIChomozygous112527646
41732650817326509GA36GENIChomozygous112527648
41732669417326695TC26GENIChomozygous112527650
41732672517326726CT25GENIChomozygous112527652
41732689617326897CT26GENIChomozygous112527654
41732732017327321GT33GENIChomozygous112527656