chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4117589547117589548AG4GENIChomozygous126022554
4117590202117590203GA19GENIChomozygous126022556
4117590287117590288AG25GENIChomozygous126022557
4117590327117590328GT26GENIChomozygous126022558
4117590361117590362AT17GENICpossibly homozygous126022559
4117590673117590674AT3GENICheterozygous126052679
4117592278117592279CT3GENICheterozygous126052680
4117592654117592655GC15GENIChomozygous126022561
4117592986117592987GA16GENIChomozygous126022562
4117593488117593489AG27GENIChomozygous126022563
4117593688117593689GA12GENIChomozygous126052681
4117593829117593830CT18GENIChomozygous126022564
4117593862117593863GT21GENIChomozygous126022565
4117594552117594553GA13GENIChomozygous126022566
4117594706117594707AG20GENIChomozygous126022567
4117595063117595064CT12GENIChomozygous126022568
4117595160117595161GA13GENIChomozygous126022569
4117595226117595227GA11GENIChomozygous126022570
4117595238117595239AG12GENIChomozygous126022571
4117595531117595532AG19GENIChomozygous126022572
4117595631117595632AT7GENIChomozygous126022573
4117595759117595760TA14GENIChomozygous126022574
4117596276117596277AG4GENICheterozygous126052682
4117598125117598126GA13GENIChomozygous126022575
4117600797117600798CT13GENIChomozygous126022576
4117601389117601390AC18GENIChomozygous126022577
4117601700117601701AG23GENIChomozygous126022578
4117601840117601841CG14GENIChomozygous126022579
4117603123117603124TC19GENIChomozygous126022580