chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266866964266866965TG41GENIChomozygous954114083
1266867306266867307GA22GENIChomozygous954114084
1266869171266869172TC29GENIChomozygous954114085
1266869354266869355CT36GENIChomozygous954114086
1266871195266871196CT46GENIChomozygous954114087
1266871799266871800AG41GENIChomozygous954114088
1266872295266872296GA31GENIChomozygous954114089
1266876378266876379AG23GENIChomozygous954114090
1266876812266876813GA34GENIChomozygous954114091
1266878355266878356CT27GENIChomozygous954114092
1266879795266879796TG27GENIChomozygous954114093
1266879804266879805AG26GENIChomozygous954114094
1266881234266881235CT28GENIChomozygous954114095
1266881721266881722AG29GENIChomozygous954114096
1266882385266882386GC27GENIChomozygous954114097
1266884148266884149CG27GENIChomozygous954114098
1266885292266885293AC47GENIChomozygous954114099
1266885604266885605GA27GENIChomozygous954114100
1266888529266888530CT11GENIChomozygous954114101
1266889651266889652TC30GENIChomozygous954114102
1266890046266890047TC36GENIChomozygous954114103
1266892447266892448AG12GENIChomozygous954114104
1266892512266892513TC15GENIChomozygous954114105
1266894775266894776GA35GENIChomozygous954114106
1266895476266895477AG30GENIChomozygous954114107
1266896747266896748TG36GENIChomozygous954114108
1266897388266897389TC12GENIChomozygous954114109
1266897506266897507GA21GENIChomozygous954114110
1266898357266898358AG19GENIChomozygous954114111
1266898962266898963GA13GENIChomozygous954114112
1266899513266899514GA23GENIChomozygous954114113
1266907705266907706AT34GENIChomozygous954114114