chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
158615602586156026AC26GENIChomozygous125780533
158615762486157625CT16GENIChomozygous125780535
158615827186158272GA13GENIChomozygous125780536
158615937186159372AG4GENIChomozygous125780537
158616069286160693AG17GENIChomozygous125780538
158616100886161009GA21GENIChomozygous125780539
158616299986163000AG29GENIChomozygous125780540
158616373886163739AG20GENIChomozygous125780541
158616615686166157GA27GENIChomozygous125780542
158616692286166923TC24GENIChomozygous125780543
158616853186168532CT17GENIChomozygous125780544
158616911686169117GA18GENIChomozygous125780545
158616932786169328CT17GENIChomozygous125780546
158616967786169678TG5GENICheterozygous125804424
158617073086170731CT10GENIChomozygous125780547
158617101686171017TC16GENIChomozygous125780548
158617174886171749AG14GENIChomozygous125780549
158617206886172069TC22GENIChomozygous125780550
158617240386172404CT19GENIChomozygous125780551
158617243086172431GT24GENIChomozygous125780552
158617735886177359TA14GENIChomozygous125780554
158617764786177648GA23GENIChomozygous125780555
158618014686180147TA14GENIChomozygous125780556
158618246386182464CT18GENIChomozygous125780557
158618280186182802CT22GENIChomozygous125780558
158618288886182889CT20GENIChomozygous125780559
158618295986182960GT17GENIChomozygous125780560
158618371286183713AG14GENIChomozygous125780561
158618599086185991TC4GENIChomozygous125780562
158618599586185996GC5GENICheterozygous125804425
158618624286186243AC31GENIChomozygous125780563
158618663386186634AG21GENIChomozygous125780564
158619108186191082AG25GENICpossibly homozygous125780565
158619148786191488AC17GENIChomozygous125780566
158619376486193765TG18GENIChomozygous125780567
158619485886194859GA11GENIChomozygous125780568
158619516486195165GA15GENIChomozygous125780569
158619758386197584GA21GENIChomozygous125780570
158619638486196385CT17GENIChomozygous125799006