chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105634358856343589A8GENICpossibly homozygous131094476
105635968656359686T19GENIChomozygous131094479
105635536156355362AG13GENIChomozygous116783432
105635801556358016AC14GENIChomozygous117059675
105636379256363793TC15GENIChomozygous117059677
105635832956358329TTATTCACTACTTTAACCTTTAAACGTGTGTGTGTGTGTGTGTGTTTTACAGGTTGGCTTTTCTTTTGTGTG10GENICpossibly homozygous131465690