chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3163703489163703490AG24GENIChomozygous111805029
3163703721163703722CA15GENIChomozygous111805031
3163705896163705897AG26GENIChomozygous111805033
3163705928163705929AG34GENIChomozygous111805035
3163706294163706295GA45GENIChomozygous111805037
3163706837163706838CT27GENIChomozygous111805039
3163712521163712522TC37GENIChomozygous111805052
3163712955163712956CG29GENIChomozygous111805054
3163715354163715355TA37GENIChomozygous111805066
3163716915163716916TA6GENIChomozygous112045781
3163718103163718104AT32GENIChomozygous111805068
3163718496163718497AG21GENIChomozygous111805070
3163721714163721715AT2GENIChomozygous111805072
3163723687163723688AG23GENIChomozygous111805076
3163726612163726613GA35GENIChomozygous111805078
3163727688163727689CT31GENIChomozygous111805080
3163727691163727692AG30GENIChomozygous111805082
3163727933163727934GA21GENIChomozygous111805084
3163730747163730748CT20GENIChomozygous111805086
3163731208163731209AG21GENIChomozygous111805088
3163731821163731822CT7GENIChomozygous111805092
3163733887163733888GA19GENIChomozygous111805100
3163734732163734733GA8GENIChomozygous111805102
3163735843163735844CT15GENIChomozygous111805106
3163738257163738258AG30GENIChomozygous111805108
3163740307163740308CT41GENIChomozygous111805118
3163741071163741072CT14GENIChomozygous111805120
3163742479163742480AC21GENIChomozygous111805124
3163742764163742765AG16GENIChomozygous111805126
3163748786163748787TG29GENIChomozygous111805128