chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4171272657171272658AG20GENIChomozygous112951669
4171367086171367087T2GENIChomozygous128104650
4171367118171367119G5GENIChomozygous128104651
4171367152171367152T6GENIChomozygous128104652
4171367158171367159G6GENIChomozygous128104653
4171366960171366961CA1GENIChomozygous135109707
4171366963171366964TC1GENIChomozygous135109708
4171366965171366966TC1GENIChomozygous135109709
4171366971171366971CACA1GENIChomozygous135108126
4171388443171388444CA10GENICheterozygous135109710
4171409298171409299TC5GENIChomozygous112951677
4171424982171424982TGCC7GENICpossibly homozygous131364730
4171433090171433091CG16GENIChomozygous112951679