chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
98709203687092037CT38GENIChomozygous68169174
98709268387092684AG37GENIChomozygous68169177
98709285387092854CT34GENIChomozygous68521438
98709321787093218TA37GENIChomozygous68169180
98709342587093426AG46GENIChomozygous68169183
98709360587093606GT35GENICpossibly homozygous68169186
98709362687093627AG32GENIChomozygous68169189
98709365587093656GA30GENIChomozygous68169192
98709369787093698GC28GENIChomozygous68169195
98709371187093712CT35GENIChomozygous68169198
98709436387094364TC31GENIChomozygous68169201
98709526687095267CA46GENIChomozygous68521440
98709627587096276AT20GENIChomozygous68521442
98709785487097855AT34GENIChomozygous68169213