chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108697497986974980TA11GENIChomozygous82720887
108697498086974981CA11GENIChomozygous82720888
108697499186974992AT7GENIChomozygous68143767
108698977086989771TA2GENIChomozygous68143815
108699389986993900TC13GENIChomozygous68143836
108699607886996079AG9GENICpossibly homozygous82720889
108699618186996182TC7GENIChomozygous68143856
108699624686996247CG10GENIChomozygous68928240
108699144986991450GT13GENIChomozygous68928232
108699254786992548GT5GENIChomozygous68928234
108699608386996084GA8GENICpossibly homozygous68928236
108699617186996172AT5GENIChomozygous68928238
108699658386996584AG5GENIChomozygous68928242
108700088987000890AG17GENIChomozygous68143865
108700593987005940CA3GENIChomozygous68143868
108700609187006092AG7GENIChomozygous68143871
108702468887024689GA17GENIChomozygous68143901
108699830986998310AT24GENIChomozygous69145171