chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2189424786189424786A21GENIChomozygous127717875
2189425759189425759ACA19GENIChomozygous127717876
2189434803189434804T26GENIChomozygous127717877
2189435371189435371TTG16GENIChomozygous127717878
2189426891189426892GA23GENIChomozygous110171517
2189428773189428774CT16GENICpossibly homozygous110171519
2189431276189431277CT21GENIChomozygous110171521
2189432345189432346TC18GENIChomozygous110171523
2189433794189433795TC13GENIChomozygous110171525
2189435873189435874CG17GENIChomozygous110171526
2189436018189436019GA22GENIChomozygous110171528
2189438797189438798G17GENIChomozygous127717879
2189440075189440076TG22GENIChomozygous110171530
2189441035189441045GTTTTGTTTT19GENIChomozygous127717880
2189444497189444498AT25GENIChomozygous110171532
2189444500189444501AG24GENIChomozygous110171534
2189448521189448522GA15GENIChomozygous110171536
2189449307189449308TC28GENIChomozygous110171538
2189450375189450376GA14GENIChomozygous110171539
2189450447189450448CT21GENIChomozygous110171541