chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123020273530202736GA2GENIChomozygous115562067
123020283030202831GA5GENIChomozygous115304175
123020285730202858GA6GENIChomozygous115304177
123020477230204773CT3GENIChomozygous115562069
123020504230205043TC5GENIChomozygous115582423
123020542530205426CT5GENIChomozygous115304179
123020548130205482TC7GENIChomozygous115304181
123020592630205927GA6GENIChomozygous115304183
123020611730206118GA6GENIChomozygous115304185
123020653030206531GA10GENIChomozygous115304189
123020660330206604CT9GENIChomozygous115304191
123020665730206658AG6GENIChomozygous115304193
123020688030206881GA7GENIChomozygous115562079
123020733030207331GA8GENIChomozygous115601830
123021052730210528GA2GENIChomozygous115304219
123021069730210698TA9GENIChomozygous115304221
123021235930212360CT9GENIChomozygous115304223
123021264430212645AG3GENIChomozygous115304225
123021277430212775TC4GENIChomozygous115304227
123021313330213134GC2GENIChomozygous115304229
123021320730213208GT5GENIChomozygous115304231
123021322330213224GA6GENIChomozygous115304233
123021345830213459CT6GENIChomozygous115304237
123021374830213749AG2GENIChomozygous115304239
123021398130213982TC2GENIChomozygous115304241
123021481130214812TA7GENIChomozygous115601834
123021530730215308GT3GENIChomozygous115601836