chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
859691785969179CG6GENIChomozygous622217435
859694465969447CA15GENIChomozygous622217436
859700835970084CG2GENIChomozygous622217437
859725785972579A-5GENICheterozygous739741506
859763365976337AACT21GENIChomozygous739741507
859763915976392TC14GENIChomozygous622217438
859772245977225TG27GENICpossibly homozygous622217439
859772275977228TC31GENIChomozygous622217440
859774315977443TGTGTGTGCGTG------------16GENIChomozygous739741508
859777235977733TGTGTGTGTT----------20GENIChomozygous739741509
859777535977754TG22GENIChomozygous622217441
859778025977804GT--28GENICpossibly homozygous739741510
859778975977898CT12GENIChomozygous622217442
859779165977917AATG16GENIChomozygous739741511
859782355978236CCGTGTGT9GENIChomozygous739741512
859782905978292AT--12GENIChomozygous739741513
859782935978295CA--12GENIChomozygous739741514
859785375978547TGTGTGTGCG----------11GENICheterozygous739741515
859785965978726GTGTGCATGTGTGTGTGCGTGTGTTTGTGTGCGTGCATGTGTGTGCGCGTGCGTGTGTGTGTTTGTGTGTGCGTGTGTGTGCGGGTGCGTGCATGTGTGTGTGCGTGCATGTGTGTGCGTGTGTGTTTGT----------------------------------------------------------------------------------------------------------------------------------20GENIChomozygous739741516
859788225978823AATGTGTG9GENIChomozygous739741517
859788545978855GT6GENIChomozygous622217443
859788635978864CCGT8GENIChomozygous739741518
859789505978958GTGAGTGC--------8GENIChomozygous739741519
859813465981347AG16GENIChomozygous622217444
859818695981891GTGTGTGTGTGTGTGTGTGTGT----------------------10GENIChomozygous739741520
859876585987659TTA5GENICheterozygous739741524
859882595988260AG20GENIChomozygous622217445
859913335991334GT26GENIChomozygous622217446
859924845992505CACTAAGGGAGATTATTCCTT---------------------19GENIChomozygous739741525
859925285992529GA18GENIChomozygous622217447
859939205993921TC22GENIChomozygous622217448
859939425993943AT17GENIChomozygous622217449
859944795994480AG32GENIChomozygous622217450