chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
98709203687092037CT29GENICpossibly homozygous68169174
98709268387092684AG35GENIChomozygous68169177
98709285387092854CT42GENIChomozygous68521438
98709321787093218TA28GENIChomozygous68169180
98709342587093426AG24GENIChomozygous68169183
98709360587093606GT33GENIChomozygous68169186
98709362687093627AG34GENIChomozygous68169189
98709365587093656GA26GENIChomozygous68169192
98709369787093698GC27GENIChomozygous68169195
98709371187093712CT33GENIChomozygous68169198
98709436387094364TC38GENIChomozygous68169201
98709526687095267CA37GENIChomozygous68521440
98709627587096276AT33GENIChomozygous68521442