chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116657485116657486GT28GENIChomozygous116669845
8116657931116657932GA22GENIChomozygous116669847
8116659319116659320CT17GENIChomozygous116669849
8116659488116659489CT17GENIChomozygous116669851
8116659556116659557CT7GENIChomozygous116669853
8116660193116660194CT32GENICpossibly homozygous116669855
8116660333116660334AG24GENIChomozygous116669857
8116661595116661596AG24GENIChomozygous116669861
8116661666116661667CT19GENIChomozygous116669863
8116661704116661705AG24GENIChomozygous116669865
8116671013116671014CT17GENIChomozygous116669877
8116671171116671172AG18GENIChomozygous116669879
8116671194116671195GA17GENIChomozygous116669881
8116674029116674030GA20GENIChomozygous116669895
8116674521116674522AC25GENIChomozygous116669897
8116674965116674966CT29GENIChomozygous116669907
8116675179116675180TC28GENIChomozygous116669909
8116675665116675666AG22GENIChomozygous116669911
8116675716116675717AG24GENIChomozygous116669913
8116677958116677959GA19GENIChomozygous116669917
8116678801116678802AG16GENIChomozygous116669919