chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
859691785969179CG16GENIChomozygous645303521
859694465969447CA22GENIChomozygous645303522
859725785972579A-4GENICheterozygous754252892
859763365976337AACT28GENIChomozygous754252893
859763915976392TC24GENIChomozygous645303523
859772245977225TG27GENICpossibly homozygous645303524
859772275977228TC35GENIChomozygous645303525
859774315977443TGTGTGTGCGTG------------8GENICpossibly homozygous754252894
859777235977733TGTGTGTGTT----------4GENIChomozygous754252895
859777535977754TG9GENIChomozygous645303526
859778025977804GT--19GENICpossibly homozygous754252896
859778975977898CT2GENIChomozygous645303527
859779165977917AATG5GENICheterozygous754252897
859782355978236CCGTGTGT7GENIChomozygous754252898
859782905978292AT--3GENIChomozygous754252899
859782935978295CA--3GENIChomozygous754252900
859785375978547TGTGTGTGCG----------18GENICheterozygous754252901
859785965978726GTGTGCATGTGTGTGTGCGTGTGTTTGTGTGCGTGCATGTGTGTGCGCGTGCGTGTGTGTGTTTGTGTGTGCGTGTGTGTGCGGGTGCGTGCATGTGTGTGTGCGTGCATGTGTGTGCGTGTGTGTTTGT----------------------------------------------------------------------------------------------------------------------------------21GENICpossibly homozygous754252902
859788225978823AATGTGTG2GENIChomozygous754252903
859788545978855GT11GENIChomozygous645303528
859788635978864CCGT14GENIChomozygous754252904
859789505978958GTGAGTGC--------31GENIChomozygous754252905
859813465981347AG27GENICpossibly homozygous645303529
859818695981891GTGTGTGTGTGTGTGTGTGTGT----------------------8GENIChomozygous754252906
859872405987241A-4GENICheterozygous754252909
859876585987659TTA12GENICpossibly homozygous754252911
859882595988260AG26GENIChomozygous645303530
859913335991334GT25GENIChomozygous645303531
859924845992505CACTAAGGGAGATTATTCCTT---------------------24GENIChomozygous754252912
859925285992529GA23GENIChomozygous645303532
859939205993921TC26GENIChomozygous645303533
859939425993943AT23GENIChomozygous645303534
859944795994480AG22GENIChomozygous645303535