chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3163703489163703490AG5GENIChomozygous111805029
3163703721163703722CA15GENIChomozygous111805031
3163705896163705897AG18GENIChomozygous111805033
3163705928163705929AG9GENIChomozygous111805035
3163706294163706295GA11GENIChomozygous111805037
3163706837163706838CT17GENIChomozygous111805039
3163707973163707974TC8GENIChomozygous111805041
3163707989163707990CT11GENIChomozygous111805043
3163710001163710002AC9GENIChomozygous111805045
3163712955163712956CG20GENICheterozygous111805054
3163713777163713778TA5GENIChomozygous111805064
3163715354163715355TA7GENIChomozygous111805066
3163716915163716916TA8GENIChomozygous112045781
3163718103163718104AT15GENIChomozygous111805068
3163718496163718497AG8GENIChomozygous111805070
3163721714163721715AT6GENICheterozygous111805072
3163723687163723688AG10GENIChomozygous111805076
3163726612163726613GA20GENIChomozygous111805078
3163727691163727692AG5GENIChomozygous111805082
3163727933163727934GA19GENIChomozygous111805084
3163730747163730748CT7GENIChomozygous111805086
3163731821163731822CT14GENIChomozygous111805092
3163733317163733318AC4GENICheterozygous119939567
3163734732163734733GA15GENIChomozygous111805102
3163735843163735844CT11GENIChomozygous111805106
3163738257163738258AG19GENIChomozygous111805108
3163740307163740308CT11GENIChomozygous111805118
3163741661163741662AG5GENIChomozygous111805122
3163742479163742480AC11GENIChomozygous111805124
3163742764163742765AG14GENIChomozygous111805126