chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
64565595945655960GA18GENIChomozygous114784687
64565599345655994TC19GENIChomozygous114784689
64565611045656111GT17GENIChomozygous114784691
64565620745656208CT12GENIChomozygous114784693
64565633645656338TT17GENIChomozygous128335288
64565635045656351TC20GENIChomozygous114784695
64565635145656352TC20GENIChomozygous114784697
64565637145656372CA17GENIChomozygous114784699
64565639445656395GT11GENIChomozygous114784701
64565640845656409TG10GENIChomozygous114784703
64565652145656522CT19GENIChomozygous114784705
64565661745656618TG20GENIChomozygous114784707
64565662345656624TC19GENIChomozygous114784709
64565669945656700TG22GENIChomozygous114784711
64565670245656703GA22GENIChomozygous114784713
64565679345656794GA26GENIChomozygous114784715
64565684645656847GT18GENIChomozygous114784717
64565689445656894A13GENIChomozygous128335289
64565697045656971CT16GENIChomozygous114784719
64565708145657081AA19GENIChomozygous128335290
64565722145657222CT20GENIChomozygous114784721
64565729845657299CT27GENIChomozygous114784723
64565730645657307CA28GENIChomozygous114784725
64565733145657335ACTT27GENIChomozygous128335291
64565739245657393CT26GENIChomozygous114784727
64565739945657414TTGGACAAAACAAAA24GENIChomozygous128335292
64565748845657489GT23GENIChomozygous114784729
64565749545657496TC24GENIChomozygous114784731
64565792445657924C15GENIChomozygous128335293
64565793145657932GA16GENIChomozygous114784733
64565993245659933TG29GENIChomozygous114784735
64566007845660079G16GENIChomozygous128335294
64566633045666331GT22GENIChomozygous114784739