chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123020273530202736GA22GENIChomozygous115562067
123020283030202831GA19GENIChomozygous115304175
123020285730202858GA18GENIChomozygous115304177
123020477230204773CT11GENIChomozygous115562069
123020478730204788CT8GENIChomozygous115562071
123020479330204794TC7GENIChomozygous115562073
123020480030204801CA7GENIChomozygous115562075
123020483330204834T3GENIChomozygous128980246
123020483630204840CCTG3GENIChomozygous128980247
123020540130205401GGC10GENIChomozygous128980249
123020542530205426CT10GENIChomozygous115304179
123020548130205482TC13GENIChomozygous115304181
123020592630205927GA19GENIChomozygous115304183
123020611730206118GA14GENIChomozygous115304185
123020653030206531GA19GENIChomozygous115304189
123020660330206604CT20GENIChomozygous115304191
123020665730206658AG19GENIChomozygous115304193
123020688030206881GA16GENIChomozygous115562079
123020733030207331GA22GENIChomozygous115601830
123020906630209067CT15GENIChomozygous115601832
123020810430208105T7GENIChomozygous131491757
123021010730210107CTCGTC18GENIChomozygous128980250
123021047730210478TC21GENIChomozygous115304217
123021052730210528GA20GENICpossibly homozygous115304219
123021061730210618T21GENIChomozygous128980251
123021069730210698TA20GENIChomozygous115304221
123021235930212360CT23GENIChomozygous115304223
123021264430212645AG12GENIChomozygous115304225
123021277430212775TC15GENIChomozygous115304227
123021313330213134GC21GENIChomozygous115304229
123021320630213206CCA29GENIChomozygous128980252
123021320730213208GT29GENIChomozygous115304231
123021322330213224GA24GENIChomozygous115304233
123021334630213347AG18GENIChomozygous115304235
123021345830213459CT28GENIChomozygous115304237
123021374830213749AG22GENIChomozygous115304239
123021398130213982TC19GENIChomozygous115304241
123021481130214812TA19GENIChomozygous115601834
123021530730215308GT15GENIChomozygous115601836