chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1119478045119478046TA25GENIChomozygous120669624
1119479071119479072CG14GENIChomozygous108197453
1119488264119488265AG23GENIChomozygous108197481
1119495134119495135TA12GENIChomozygous108739160
1119495135119495136GT12GENIChomozygous108739161
1119495181119495182AG14GENIChomozygous108197541
1119495402119495403GT19GENIChomozygous108197542
1119495786119495787GA17GENIChomozygous108197543
1119496464119496465AC11GENIChomozygous108197545
1119497376119497377TA15GENIChomozygous108197547
1119497445119497446CG16GENIChomozygous108197548
1119497642119497643CA23GENIChomozygous108197551
1119498194119498195AC21GENIChomozygous108197553
1119498466119498467AC20GENIChomozygous108197554
1119498534119498535CG20GENIChomozygous108197555
1119498861119498862AG25GENIChomozygous108197560
1119499000119499001GA20GENIChomozygous108197561
1119499069119499070CT24GENIChomozygous108197562
1119500665119500666TG27GENIChomozygous108197565
1119516311119516312GA20GENIChomozygous108197582
1119522223119522224AG17GENIChomozygous108197589
1119522262119522263CT15GENIChomozygous108197590
1119524183119524184CT23GENIChomozygous108197608
1119524975119524976AG21GENIChomozygous108197609
1119531995119531996GA27GENIChomozygous108197646
1119537906119537907AT26GENIChomozygous108197690
1119538366119538367CT24GENICpossibly homozygous108197701
1119541057119541058TG15GENIChomozygous108197745
1119544826119544827AG19GENIChomozygous108197774
1119545470119545471TC25GENIChomozygous108197778
1119548972119548973TG14GENIChomozygous108197824
1119550902119550903TC9GENIChomozygous108197859
1119551840119551841AT25GENIChomozygous108197860
1119551862119551863GC16GENIChomozygous108197861
1119566192119566193TA11GENIChomozygous108197885