chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
132592876025928761AG13GENIChomozygous790971715
132592876325928764AG14GENICheterozygous790971716
132592876625928767AG13GENICheterozygous790971717
132592959225929593GC25GENIChomozygous790971718
132593001425930015CG31GENIChomozygous790971719
132593147225931473TC9GENIChomozygous790971720
132593148725931488GA8GENIChomozygous790971721
132593152525931526AC12GENICheterozygous790971722
132593154225931543CA15GENICheterozygous790971723
132593209825932099AG31GENICpossibly homozygous790971724
132593396825933969AG21GENIChomozygous790971725
132593470925934710GT32GENIChomozygous790971726
132593570825935709CT19GENIChomozygous790971727
132593592225935923GA24GENIChomozygous790971728
132593697225936973CG9GENICheterozygous790971729
132593698325936984CT7GENICheterozygous790971730
132593969025939691CT17GENIChomozygous790971731
132593998125939982CG16GENIChomozygous790971732
132594018025940181CA14GENIChomozygous790971733
132594036925940370GA10GENIChomozygous790971734
132594109525941096TC30GENIChomozygous790971735
132594119525941196CA24GENIChomozygous790971736
132594120825941209CT30GENIChomozygous790971737
132594173625941737AG39GENIChomozygous790971738
132594208425942085CT14GENIChomozygous790971739
132594308125943082GA34GENIChomozygous790971740
132594554825945549CT20GENIChomozygous790971741
132594768325947684CG9GENIChomozygous790971742
132594982425949825TA19GENIChomozygous790971743