chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
471237927123793GC17GENIChomozygous112480879
471240307124031TC16GENIChomozygous112480881
471243377124338AG31GENIChomozygous112480883
471251867125187AG20GENIChomozygous112480887
471252877125288AG22GENIChomozygous112480889
471263747126375GA17GENIChomozygous112480891
471276117127612GA34GENICheterozygous112480893
471284677128468AT18GENIChomozygous112480895
471307727130773AG23GENIChomozygous112480897
471312027131203GA19GENIChomozygous112480899
471314727131473GT26GENIChomozygous112480901
471327487132749CT23GENIChomozygous112480903
471328977132898TC22GENIChomozygous112480905
471337527133753GA24GENIChomozygous112480907
471338377133838AT24GENICpossibly homozygous112480909
471339667133967TG21GENICpossibly homozygous112480911
471340797134080TC32GENIChomozygous112480913
471353647135365GA47GENICheterozygous112480917