chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104706760647067607GA8GENIChomozygous932861675
104706797347067974AC14GENIChomozygous932861676
104708237347082374GA6GENIChomozygous932861677
104708241747082418AC12GENIChomozygous932861678
104708255747082558GA4GENIChomozygous932861679
104708275547082756TG11GENIChomozygous932861680
104708308147083082GA15GENIChomozygous932861681
104708432247084323AG10GENIChomozygous932861682
104708446147084462TC9GENIChomozygous932861683
104708587347085874TC11GENIChomozygous932861684
104708642247086423GC10GENIChomozygous932861685
104708650047086501AG11GENIChomozygous932861686
104708665247086653CA11GENIChomozygous932861687
104708819347088194GT10GENIChomozygous932861688
104708985847089859GA15GENIChomozygous932861689
104708996147089962TC6GENIChomozygous932861690
104709009547090096TA6GENIChomozygous932861691
104709048247090483TC10GENIChomozygous932861692
104709050647090507GT7GENIChomozygous932861693
104709079447090795CA11GENIChomozygous932861694
104709128847091289GT13GENIChomozygous932861695
104709153347091534CT15GENIChomozygous932861696
104709154247091543CT16GENIChomozygous932861697
104709168447091685GA9GENIChomozygous932861698
104709189647091897CT16GENIChomozygous932861699
104709296347092964TC9GENIChomozygous932861700
104709340447093405TC13GENIChomozygous932861701
104709370847093709TC14GENIChomozygous932861702
104709401947094020TC8GENIChomozygous932861703
104709540047095401AC9GENIChomozygous932861704
104709700447097005TC11GENIChomozygous932861705
104710045347100454CT7GENIChomozygous932861706
104710112647101127CT10GENIChomozygous932861707
104710113147101132CT11GENIChomozygous932861708
104710175847101759CT5GENIChomozygous932861709
104710532847105329TC12GENIChomozygous932861710
104710603047106031TC10GENIChomozygous932861711
104710799847107999AG19GENIChomozygous932861712
104710810447108105CG10GENIChomozygous932861713