chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5173340455173340456AG19GENIChomozygous798680083
5173341068173341069CT43GENIChomozygous798680084
5173342937173342938GC32GENICpossibly homozygous798680085
5173344718173344719CT24GENIChomozygous798680086
5173345388173345389GA25GENIChomozygous798680087
5173345461173345462GA25GENIChomozygous798680088
5173345467173345468GA23GENIChomozygous798680089
5173345503173345504CT33GENIChomozygous798680090
5173347147173347148AG32GENIChomozygous798680091
5173347178173347179TC26GENIChomozygous798680092
5173347309173347310TA53GENIChomozygous798680093
5173347489173347490TC49GENIChomozygous798680094
5173347683173347684AG51GENIChomozygous798680095
5173348062173348063GT19GENIChomozygous798680096
5173348303173348304GA39GENIChomozygous798680097
5173348372173348373AG38GENIChomozygous798680098
5173348932173348933GA40GENIChomozygous798680099
5173349421173349422TA49GENIChomozygous798680100
5173349703173349704AG30GENIChomozygous798680101
5173349906173349907AC58GENIChomozygous798680102
5173350381173350382TC30GENIChomozygous798680103
5173350440173350441GA42GENIChomozygous798680104
5173352655173352656CT34GENIChomozygous798680105
5173352692173352693AG35GENIChomozygous798680106
5173352901173352902TC31GENIChomozygous798680107
5173354070173354071GA21GENIChomozygous798680108