chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
370931977093198GA21GENIChomozygous990351739
370975427097543GT24GENIChomozygous990351740
370982957098296CT15GENIChomozygous990351741
370983697098370CT20GENIChomozygous990351742
370986107098611TC25GENIChomozygous990351743
370998187099819GA17GENIChomozygous990351744
371009827100983AG14GENIChomozygous990351745
371029677102968GA11GENIChomozygous990351746
371041137104114GA18GENIChomozygous990351747
371045037104504TC9GENIChomozygous990351748
371046957104696CG16GENIChomozygous990351749
371053917105392CT17GENIChomozygous990351750
371054717105472GT8GENIChomozygous990351751
371061967106197AG21GENIChomozygous990351752
371076927107693GC29GENIChomozygous990351753
371079687107969CT10GENIChomozygous990351754
371081327108133TC9GENIChomozygous990351755
371083637108364TC19GENIChomozygous990351756
371090407109041CT16GENIChomozygous990351757
371090547109055TC15GENIChomozygous990351758
371091197109120CT21GENIChomozygous990351759
371096387109639AG26GENIChomozygous990351760
371110267111027GA13GENIChomozygous990351761
371131207113121CT17GENIChomozygous990351762
371141837114184GA20GENIChomozygous990351763
371143847114385CT26GENIChomozygous990351764
371169797116980AG8GENIChomozygous990351765
371172097117210GA17GENIChomozygous990351766
371188117118812CG18GENIChomozygous990351767
371194767119477GA17GENIChomozygous990351768
371239877123988GA18GENIChomozygous990351769
371273627127363AG13GENIChomozygous990351770
371285287128529AT24GENIChomozygous990351771