chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123035349030353491TG12GENICheterozygous50170346
123035352430353526AG--9GENICheterozygous50170348
123035354030353541GA9GENICheterozygous50170350
123035354930353550TC9GENICheterozygous50170352
123035355930353560AC9GENICheterozygous50170354
123035359130353592TC9GENICheterozygous50170356
123035711530357116GA31GENICheterozygous50170426
123037073030370731CCA67GENICheterozygous50170460
123043938130439382GA15GENICheterozygous50170474
123043947130439472TG16GENICheterozygous50170476
123043947330439474TC18GENICheterozygous50170478
123044067230440673T-9GENICheterozygous50170480
123055320330553204AG10GENICheterozygous50170746
123057547530575476TA29GENICheterozygous50170990
123059439430594395AAT36GENICheterozygous50171269
123060392430603925CT42GENICheterozygous50171368
123066773430667735AG24GENICheterozygous50171785
123067382930673830CCTT71GENICheterozygous50376467
123067420130674202CT24GENICheterozygous50376471
123068393530683936AG13GENICheterozygous50171876
123068606230686063GA41GENICheterozygous50670799
123068608430686085CA31GENICheterozygous50670801
123069566230695663TTC48GENICheterozygous50670817
123070300630703007GA18GENICheterozygous51147898
123070305830703059TC18GENICheterozygous50376615
123071088930710891AA--12GENICheterozygous51147899
123072593430725935A-22GENICheterozygous50376977
123072607030726071CT8GENICheterozygous50670906
123075757530757576CT39GENICheterozygous51147900
123077141430771415GA23GENICheterozygous50172076
123077149930771500CA28GENICheterozygous50172077
123077175130771752AT17GENICheterozygous50172079
123088996730889968TG12GENICheterozygous50421240
123091396330913964TC8GENICheterozygous50172618
123091401830914019AG8GENICheterozygous50172619
123092227530922276AG16GENICheterozygous50421291