chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5155064781155064782CCTTT17GENICheterozygous56687215
5155065598155065599TG10GENIChomozygous55803829
5155065613155065614CT10GENIChomozygous55803830
5155065627155065628A-7GENIChomozygous55803831
5155072256155072257AAC10GENICheterozygous56532969
5155075197155075198GT16GENIChomozygous55803834
5155075199155075200GT16GENIChomozygous55803835
5155075202155075203GC14GENIChomozygous55803836
5155075205155075206AG14GENIChomozygous55803837
5155075228155075229GT9GENIChomozygous55803838
5155075229155075230GC10GENIChomozygous55803839
5155075245155075246AC10GENIChomozygous56461899
5155075247155075248CT9GENIChomozygous56461900
5155075260155075261AT9GENIChomozygous55803840
5155075272155075273AT8GENIChomozygous55803841
5155075308155075309TC5GENIChomozygous55803842
5155075417155075418AAG10GENIChomozygous55803843
5155075425155075426G-11GENIChomozygous55803844
5155075442155075443C-12GENIChomozygous55803845
5155076984155076985C-1GENIChomozygous56461901