chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2189047882189047883CT28GENICpossibly homozygous110170751
2189050012189050013AC16GENIChomozygous110170753
2189050556189050557CA25GENIChomozygous110170755
2189051443189051444GA11GENIChomozygous110170756
2189051494189051624ATATCTGGTTTTGGGGCTGGGGATTTAGCTCAAGTCAAGAGCGCTTACCTAGGAAGCACAAGGCCCTGGGTTCGGTCCCTAGCTCCGGGGGAAAAAAAAAAAAAAAAAAAGAACAAAAAAAAATATATAT13GENICheterozygous129869166
2189052847189052848CG21GENIChomozygous110170758
2189053171189053172TG17GENIChomozygous110170760
2189054229189054230TG21GENIChomozygous110170762
2189059518189059519GA19GENIChomozygous110170766
2189059828189059829CT19GENIChomozygous110170768
2189060873189060874GA16GENIChomozygous110170770
2189061935189061936AG13GENIChomozygous110170771
2189062544189062545CG30GENIChomozygous110170773
2189064072189064073TC22GENIChomozygous110170775
2189065618189065619CT14GENIChomozygous110170777
2189074382189074383CA19GENIChomozygous110170790
2189066659189066660AC21GENIChomozygous110170779
2189067006189067007GA22GENIChomozygous110170781
2189070061189070062GA21GENIChomozygous110170783
2189071026189071027AG23GENIChomozygous110170784
2189071120189071121GA24GENIChomozygous110170786
2189072990189072991TG19GENIChomozygous110170788
2189077022189077023TC23GENIChomozygous110170792
2189078879189078880AG17GENIChomozygous110170794
2189079578189079579TC25GENIChomozygous110170796
2189080004189080005GA22GENIChomozygous110170798
2189080586189080587GA19GENIChomozygous110170800
2189082166189082167CT18GENIChomozygous110170802
2189082214189082215AG17GENIChomozygous110170803
2189082436189082437GA29GENIChomozygous110170805
2189053266189053266G8GENICheterozygous127717635