chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108697497986974980TA10GENICpossibly homozygous82720887
108697498086974981CA9GENIChomozygous82720888
108697499186974992AT8GENIChomozygous68143767
108698977086989771TA13GENICpossibly homozygous68143815
108699389986993900TC15GENIChomozygous68143836
108699607886996079AG17GENICpossibly homozygous82720889
108699608386996084GA17GENICpossibly homozygous68928236
108699144986991450GT26GENICpossibly homozygous68928232
108699254786992548GT22GENIChomozygous68928234
108699617186996172AT20GENICpossibly homozygous68928238
108699618186996182TC19GENIChomozygous68143856
108699624686996247CG21GENIChomozygous68928240
108699658386996584AG19GENIChomozygous68928242
108700088987000890AG15GENIChomozygous68143865
108700609187006092AG10GENIChomozygous68143871
108702468887024689GA18GENICpossibly homozygous68143901
108699830986998310AT18GENIChomozygous69145171