chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151741001151741002CT18GENIChomozygous126313132
5151743016151743017AG6GENIChomozygous126313133
5151743059151743060GA19GENIChomozygous126313134
5151743295151743296AG18GENIChomozygous126313135
5151744271151744272GT16GENIChomozygous126313136
5151744454151744455CT17GENIChomozygous126313137
5151744520151744521CT25GENIChomozygous126313138
5151745207151745208CT6GENIChomozygous126313139
5151747046151747047GA4GENICheterozygous126313140
5151747051151747052GA5GENICheterozygous126313141
5151747656151747657CT8GENIChomozygous126313142
5151747786151747787GA9GENIChomozygous126313143
5151747898151747899AG13GENIChomozygous126313144
5151749349151749350CT11GENIChomozygous126313145
5151750815151750816AG8GENIChomozygous126313146
5151751828151751829TC6GENIChomozygous126313147
5151752626151752627TG18GENIChomozygous126313148
5151745976151745977GC17GENIChomozygous126206184
5151745940151745941TA21GENIChomozygous126206183