chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
173488727534887276TC45GENIChomozygous111032961
173488936034889361AC14GENIChomozygous111032963
173489211834892119AG61GENIChomozygous111032965
173489267434892675CT48GENIChomozygous111032967
173489309034893091AG46GENIChomozygous111032969
173489328534893286TC54GENIChomozygous111032971
173489568334895684GA28GENIChomozygous111195913
173489549834895499GA24GENIChomozygous119281028
173489551034895511GA27GENIChomozygous119281030
173489555334895554TA28GENIChomozygous119281032
173489555834895559TC28GENIChomozygous119281034
173489556534895566CA29GENIChomozygous119281036
173489556734895568TA29GENIChomozygous119281038
173489544034895441GA18GENIChomozygous111304570
173489552134895522C26GENIChomozygous129445197
173489875134898752A59GENIChomozygous129445198
173489945834899459CT46GENIChomozygous111032973
173489948234899483TC50GENIChomozygous111032975
173489954234899543A51GENICpossibly homozygous129445199
173489972334899724TC48GENIChomozygous111032977
173489974934899750GA42GENIChomozygous111032979
173489982634899827AG37GENIChomozygous111032981
173489985834899859AG35GENIChomozygous111032983
173489992834899929CT38GENIChomozygous111032985
173489998234899983AG47GENIChomozygous111032987
173490047934900480GA55GENIChomozygous111032989
173490059234900593C48GENIChomozygous129445200
173490069934900700CT51GENIChomozygous111032991
173490076734900768CT56GENIChomozygous111032993
173490097034900971GC53GENIChomozygous111032995
173490229034902291CT38GENIChomozygous111304571
173490242734902428CT55GENIChomozygous111032997
173490340734903408TA33GENIChomozygous111032999
173490447734904478GA49GENIChomozygous111033001
173490477734904778AC51GENIChomozygous111033003
173490499434904999GGGGA10GENICheterozygous129445201