chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96165858961658590TC40GENIChomozygous117543017
96165859961658600CT37GENIChomozygous117543019
96165866361658664CT51GENIChomozygous117358638
96166430561664306GT94GENIChomozygous117543021
96166519761665198AG48GENICpossibly homozygous117543023
96166532961665330GA44GENIChomozygous117543025
96166881861668819AG183GENICheterozygous117543027
96166883861668839TA178GENICheterozygous117543029
96166886561668866AC200GENICheterozygous117543031
96166887361668874AG206GENICheterozygous117358664
96166888061668881AG205GENICheterozygous117543033
96166888561668886CA209GENICheterozygous117543035
96166890961668910AG195GENICheterozygous117543037
96166893961668940AC161GENICheterozygous117543039
96166895461668955AC126GENICheterozygous117543041
96166896561668966AG111GENICheterozygous117358669
96166898361668984CT83GENICheterozygous117543043
96166898761668988TA79GENICheterozygous117358670
96166899361668994GA73GENICheterozygous117543045
96166987761669878CT199GENICheterozygous117543047
96167254061672541CT59GENIChomozygous117358677
96167308661673087GC58GENIChomozygous117358679