chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
137025966370259664TC48GENIChomozygous930170831
137026155570261556AT44GENIChomozygous930170832
137026430570264306GA35GENIChomozygous930170833
137026717670267177GC31GENIChomozygous930170834
137026731570267316CT35GENIChomozygous930170835
137026877670268777GA18GENIChomozygous930170836
137026936370269364CA26GENIChomozygous930170837
137026945270269453CA25GENIChomozygous930170838
137027185070271851TC34GENIChomozygous930170839
137027356470273565TA35GENIChomozygous930170840
137027550770275508CT21GENIChomozygous930170841
137027612970276130TC33GENIChomozygous930170842
137027924670279247GA23GENIChomozygous930170843
137027954770279548TC28GENIChomozygous930170844
137027955270279553AT35GENIChomozygous930170845
137028235070282351CG31GENIChomozygous930170846
137028476270284763CT38GENIChomozygous930170847
137028518770285188CT37GENIChomozygous930170848
137028576470285765CT19GENIChomozygous930170849
137029131270291313AG50GENIChomozygous930170850
137029164170291642GA34GENIChomozygous930170851
137029435870294359GA20GENIChomozygous930170852
137029818170298182AG22GENIChomozygous930170853
137030101070301011GC48GENIChomozygous930170854
137030240870302409CT31GENIChomozygous930170855
137030285470302855GA18GENIChomozygous930170856
137030431170304312GA32GENIChomozygous930170857
137030485870304859AG35GENIChomozygous930170858
137030611270306113CT30GENIChomozygous930170859
137030622870306229AG25GENIChomozygous930170860
137030676870306769CT18GENIChomozygous930170861
137030705870307059CG43GENIChomozygous930170862
137030737270307373AG29GENIChomozygous930170863
137030758070307581CG16GENIChomozygous930170864
137031143870311439AG41GENIChomozygous930170865
137031293070312931TC32GENIChomozygous930170866
137031513170315132GA40GENIChomozygous930170867
137031704770317048GA15GENIChomozygous930170868