chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171358900613589007GA10GENIChomozygous111169607
171358906813589069GA7GENIChomozygous111169609
171358949013589491CT17GENIChomozygous119265564
171358955513589556TG9GENIChomozygous119265565
171358994113589942TC13GENIChomozygous111169613
171359000313590004CG17GENIChomozygous111169615
171359004113590042GT7GENIChomozygous111315278
171359028013590281TC11GENIChomozygous119265566
171359125713591258TC21GENIChomozygous111169617
171359152913591530TA15GENIChomozygous111169619
171359261013592611GT28GENIChomozygous110963805
171359271613592717CA35GENICpossibly homozygous111169621
171359275113592752AG30GENICpossibly homozygous111169623
171359292513592926AG17GENIChomozygous111169625
171359293013592931GA17GENIChomozygous111169627
171359301413593015GA29GENIChomozygous111169629