chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1014652081465209TC40GENIChomozygous116466666
1014668131466814GA30GENIChomozygous116466668
1014718871471888GA35GENIChomozygous116466670
1014721551472156AT30GENIChomozygous116466672
1014721891472190GT26GENIChomozygous116466674
1014726421472643CT29GENIChomozygous116466676
1014735291473530CA29GENIChomozygous116466678
1014752431475244CA51GENICpossibly homozygous116466680
1014763361476337GA32GENIChomozygous116466682
1014764241476425CG36GENIChomozygous116466684
1014790841479085GC38GENIChomozygous116466686
1014791791479180AG42GENIChomozygous116466688
1014792811479282GA26GENIChomozygous116466690
1014796571479658AG25GENIChomozygous116466692
1014797961479797TC36GENIChomozygous116466694
1014802841480285GA27GENIChomozygous116466696
1014810441481045CT42GENIChomozygous116466698
1014815831481584TC30GENIChomozygous116466700
1014821361482137TC38GENIChomozygous116466702
1014822801482281AT28GENIChomozygous116466704
1014858851485886GC28GENIChomozygous116466706
1014880921488093CT28GENIChomozygous116466708
1014899951489996AG21GENICheterozygous116466710
1014899991490000AG21GENICheterozygous116466712
1014900031490004AG26GENICheterozygous116466714
1014916141491615GA48GENIChomozygous116466716
1014917421491743TA63GENIChomozygous116466718
1014963781496379AG45GENIChomozygous116466720