chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5173341068173341069CT45GENICpossibly homozygous966892049
5173342937173342938GC23GENIChomozygous966892050
5173344718173344719CT36GENICpossibly homozygous966892051
5173345388173345389GA28GENIChomozygous966892052
5173345467173345468GA33GENIChomozygous966892053
5173345503173345504CT38GENIChomozygous966892054
5173347147173347148AG34GENIChomozygous966892055
5173347178173347179TC43GENIChomozygous966892056
5173347309173347310TA30GENIChomozygous966892057
5173347489173347490TC38GENIChomozygous966892058
5173347683173347684AG40GENIChomozygous966892059
5173348062173348063GT27GENIChomozygous966892060
5173348303173348304GA23GENIChomozygous966892061
5173348372173348373AG19GENIChomozygous966892062
5173348932173348933GA36GENIChomozygous966892063
5173349421173349422TA38GENIChomozygous966892064
5173349703173349704AG41GENIChomozygous966892065
5173349906173349907AC50GENIChomozygous966892066
5173350381173350382TC19GENIChomozygous966892067
5173350440173350441GA28GENIChomozygous966892068
5173352655173352656CT29GENICpossibly homozygous966892069
5173352692173352693AG26GENIChomozygous966892070
5173352901173352902TC28GENIChomozygous966892071
5173354070173354071GA24GENIChomozygous966892072