chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6102032297102032298GA70GENIChomozygous114919135
6102032524102032525AG75GENICpossibly homozygous114919136
6102032684102032685TC56GENICpossibly homozygous114919137
6102032794102032795AG53GENIChomozygous114919138
6102032823102032824GA61GENIChomozygous114919139
6102033111102033112AG60GENICpossibly homozygous114919140
6102035697102035698CT60GENIChomozygous114919141
6102039637102039638CT73GENIChomozygous114919142
6102041318102041319GA61GENIChomozygous114919143
6102041953102041954TA67GENIChomozygous114919144
6102042493102042494TC48GENIChomozygous114919145
6102045123102045124AT46GENICpossibly homozygous114919146
6102045646102045647GC58GENIChomozygous114919147
6102046598102046599GA74GENIChomozygous114919148