chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99995554699955547AG11GENICpossibly homozygous52075609
99995578499955785TC11GENIChomozygous52075611
99995598199955982CT10GENICpossibly homozygous52075615
99995810799958108TC14GENICpossibly homozygous52772472
99995857299958573AG5GENIChomozygous52075629
99995891699958917TG9GENIChomozygous52075631
99995928499959285TC13GENIChomozygous52075633
99995979799959798GA18GENIChomozygous52772474
99995986899959869C-10GENIChomozygous52075635
99996067099960671TC6GENIChomozygous52075639
99996079799960798TC4GENIChomozygous52772476
99996085299960853CG11GENICpossibly homozygous52772478
99996203299962033GA7GENIChomozygous52772480
99996213499962135CA10GENIChomozygous52772482
99996223799962238CT16GENICpossibly homozygous52772484
99996227599962276GA10GENIChomozygous52075645
99996279399962794CT10GENIChomozygous52772486
99996354499963545AG9GENICpossibly homozygous52075647
99996357999963580CA8GENIChomozygous52772488
99996358599963586CT8GENIChomozygous52772490
99996381999963820CT7GENIChomozygous52075651
99996490499964905AG5GENIChomozygous52075657
99996544099965441CA9GENICpossibly homozygous52772492