chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117026805117026806TG15GENICheterozygous116341035
7117026832117026836GGAG21GENICheterozygous134835289
7117026837117026840TGG22GENICheterozygous134835290
7117026842117026843AT21GENICheterozygous134838793
7117026844117026848CGAA21GENICheterozygous134835291
7117026852117026853G22GENICheterozygous134835292
7117026861117026862AG25GENICheterozygous134838794
7117027368117027369TA37GENICpossibly homozygous116341037
7117027545117027546GA23GENIChomozygous134838795
7117028201117028202CG22GENICpossibly homozygous116341039
7117028283117028283TT3GENIChomozygous134835293
7117028284117028284TTTGATCACGCTAGATAAGATAATTGTGGGCGTGCCTTTGAGGAATTTTT3GENIChomozygous134835294
7117029050117029051AG7GENIChomozygous115846117
7117029096117029097AG12GENIChomozygous134838796
7117029312117029313GA7GENIChomozygous116341041
7117029807117029808GT16GENICheterozygous134838797
7117030146117030147C13GENIChomozygous134835295
7117027919117027920GA8GENIChomozygous116393555
7117029786117029787CA18GENICheterozygous116224749
7117029813117029814CT16GENICheterozygous128562327
7117029845117029846TG22GENIChomozygous128562328
7117030933117030934TG15GENIChomozygous116341043
7117030938117030939TC14GENIChomozygous116301952
7117031331117031332CA46GENIChomozygous116341045
7117031349117031350CG48GENIChomozygous116341047
7117031833117031834AG53GENIChomozygous115846119
7117032408117032409TC44GENICpossibly homozygous116341049
7117032484117032485TC30GENIChomozygous115846121
7117032582117032583AG40GENICheterozygous115846123
7117032667117032668CT26GENICheterozygous134838798