chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71231692512316926G-21GENIChomozygous54630137
71231731712317318TC33GENIChomozygous53790714
71232013412320135GC31GENIChomozygous54630139
71232081912320820TTC27GENIChomozygous54630141
71232090912320910TC27GENIChomozygous53790718
71232213012322142GTGTGTGTGTGT------------36GENIChomozygous55071022
71232293512322936GGCTGTCTGTCTGTCTGTCTGT33GENIChomozygous55071024
71232553612325537GA27GENIChomozygous54630145
71232576012325761AG31GENIChomozygous54630147
71232622512326226GA37GENIChomozygous54630149
71232643512326436GGC11GENIChomozygous53790723
71232726312327264GA32GENIChomozygous54630151
71232853812328539GA28GENIChomozygous54630153
71232939012329392AG--27GENIChomozygous54630155
71232996212329963CT28GENIChomozygous54630157
71233098212330983GA42GENIChomozygous54630159
71233139912331400AG40GENIChomozygous53790727
71233151312331514AG43GENIChomozygous54630161
71233251012332511CT23GENIChomozygous54630163
71233308012333084GCCT----19GENIChomozygous54630165
71233332112333322GC33GENIChomozygous53790728
71233335212333363GTGGACATTGT-----------30GENIChomozygous54630167
71233354112333545GTGA----33GENIChomozygous54630171
71233562612335627AACACTCACTGTCCCCAC1GENIChomozygous55021173
71233832112338322AAT13GENIChomozygous53790738