chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266866964266866965TG9GENIChomozygous108638724
1266867306266867307GA18GENIChomozygous108638725
1266871799266871800AG28GENIChomozygous108638729
1266872295266872296GA23GENIChomozygous108638730
1266876378266876379AG21GENIChomozygous108638732
1266876812266876813GA21GENIChomozygous108638733
1266877785266877786CT21GENIChomozygous120694766
1266877967266877968CT24GENIChomozygous125472186
1266879795266879796TG19GENIChomozygous108638735
1266881585266881586CT24GENIChomozygous125472187
1266881721266881722AG17GENIChomozygous108638738
1266882385266882386GC6GENIChomozygous108638739
1266884148266884149CG20GENIChomozygous108638740
1266885292266885293AC13GENIChomozygous108638741
1266885604266885605GA16GENIChomozygous108638742
1266885897266885898TC14GENIChomozygous108638743
1266887077266887078GA13GENIChomozygous108638760
1266888529266888530CT11GENIChomozygous108638761
1266890046266890047TC26GENIChomozygous108638764
1266891799266891800AT8GENIChomozygous125472188
1266892512266892513TC17GENIChomozygous108638765
1266894775266894776GA25GENIChomozygous108638767
1266895476266895477AG24GENIChomozygous108638768
1266897388266897389TC4GENIChomozygous108638770
1266897506266897507GA15GENIChomozygous108638771
1266899513266899514GA20GENIChomozygous108638774
1266901546266901547GA4GENIChomozygous125472189
1266906928266906929AC18GENIChomozygous120694774
1266907705266907706AT10GENIChomozygous108638775