chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167067738070677386GTGTGT------5GENIChomozygous48050275
167068305970683060T-8GENIChomozygous47851110
167068720170687202CT15GENICpossibly homozygous47851111
167068919170689192AT14GENIChomozygous47851112
167069067870690684TTTTGT------4GENIChomozygous47851113
167069222170692222AATGTG4GENIChomozygous47511591
167069248370692485TG--1GENIChomozygous47851114
167069306370693064T-9GENIChomozygous47820706
167069378970693790AG13GENIChomozygous47691777
167069453270694533CT7GENIChomozygous47691778
167069531170695312GA9GENIChomozygous47851115
167069541470695415CT17GENIChomozygous47851116
167069607670696090ACACACACACACAC--------------7GENICheterozygous47997459
167069634670696347TC15GENIChomozygous47691779
167069754270697543GGCAGGACAGGA4GENIChomozygous47691780