chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123020253530202536T12GENICheterozygous130781210
123020273530202736GA9GENIChomozygous115562067
123020283030202831GA13GENIChomozygous115304175
123020285730202858GA15GENIChomozygous115304177
123020477230204773CT13GENIChomozygous115562069
123020478730204788CT11GENIChomozygous115562071
123020479330204794TC10GENIChomozygous115562073
123020480030204801CA11GENIChomozygous115562075
123020483330204834T14GENIChomozygous128980246
123020483630204840CCTG15GENIChomozygous128980247
123020540130205401GGC8GENIChomozygous128980249
123020542530205426CT7GENIChomozygous115304179
123020548130205482TC6GENIChomozygous115304181
123020592630205927GA10GENIChomozygous115304183
123020611730206118GA16GENIChomozygous115304185
123020653030206531GA17GENIChomozygous115304189
123020660330206604CT20GENIChomozygous115304191
123020665730206658AG16GENIChomozygous115304193
123020688030206881GA15GENIChomozygous115562079
123021010730210107CTCGTC21GENIChomozygous128980250
123021047730210478TC13GENIChomozygous115304217
123021052730210528GA17GENIChomozygous115304219
123021061730210618T25GENIChomozygous128980251
123021069730210698TA14GENIChomozygous115304221
123021235930212360CT16GENIChomozygous115304223
123021264430212645AG16GENIChomozygous115304225
123021277430212775TC12GENIChomozygous115304227
123021313330213134GC10GENIChomozygous115304229
123021320630213206CCA10GENIChomozygous128980252
123021320730213208GT10GENIChomozygous115304231
123021322330213224GA16GENIChomozygous115304233
123021334630213347AG16GENIChomozygous115304235
123021345830213459CT12GENIChomozygous115304237
123021374830213749AG12GENIChomozygous115304239
123021398130213982TC15GENIChomozygous115304241
123020733030207331GA20GENIChomozygous115601830
123020906630209067CT14GENIChomozygous115601832
123021481130214812TA18GENIChomozygous115601834
123021530730215308GT17GENIChomozygous115601836
123020810430208105T10GENIChomozygous131491757