chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
143565137335651374TC49GENIChomozygous113422034
143565141835651419CT47GENICpossibly homozygous113422035
143565218635652187AC16GENIChomozygous113422036
143565234535652346CG18GENIChomozygous113422037
143565240535652406AG27GENIChomozygous113422038