chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75707918057079181GT29GENIChomozygous138091589
75707922857079229TC19GENIChomozygous138091590
75708072157080722AG24GENIChomozygous138091591
75708119457081194AGAGGG24GENIChomozygous137954407
75708215557082156GA28GENIChomozygous138091592
75708366557083666AG20GENIChomozygous138091596
75708298757082988AG34GENIChomozygous138091593
75708298857082989TG34GENIChomozygous138091594
75708324157083242GC26GENIChomozygous138091595
75708494757084948TA39GENIChomozygous138091597
75708759157087592CT17GENIChomozygous138091598
75708799057087991TC19GENIChomozygous138091599
75709016557090166GA25GENIChomozygous138091600
75709071457090715TC17GENIChomozygous138091601
75709077057090771TC19GENIChomozygous138091602
75709284857092849CT23GENIChomozygous138091603
75709494057094941CT32GENIChomozygous138091604
75709597257095973CT19GENIChomozygous138091605
75709662557096625T14GENICheterozygous137954408
75709666157096662CT19GENICheterozygous138091606
75709667257096673CT20GENICheterozygous138091607
75709841757098418GA26GENIChomozygous138091608
75710097857100979CT30GENIChomozygous138091609
75710112757101128TC41GENIChomozygous138091610
75710489157104892TC16GENIChomozygous138091611
75710646557106466AG21GENIChomozygous138091612
75710764057107641AG23GENIChomozygous138091613
75710844357108444AG13GENIChomozygous138091614
75710878157108782T10GENIChomozygous403211795
75710878157108782TC10GENICheterozygous403211796
75710877957108780T10GENIChomozygous403211793
75710877957108780TC10GENICheterozygous403211794
75710878357108784T10GENIChomozygous403211797
75710878357108784TC10GENICheterozygous403211798
75710878557108786T10GENIChomozygous403211799
75710878557108786TC10GENICheterozygous403211800
75710894157108942TC28GENIChomozygous138091615
75710906257109065CTC15GENIChomozygous137954409
75710998457109985CT23GENIChomozygous138091616