chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2040548054054806TTTTTG3GENICheterozygous45374703
2040551524055153CCAA19GENIChomozygous45374705
2040557234055724CT21GENIChomozygous45374706
2040563084056309TC17GENIChomozygous45374707
2040568814056882AG22GENICpossibly homozygous45374708
2040583464058347GA26GENIChomozygous45374710
2040585854058586CT23GENICpossibly homozygous45374711
2040591054059106CT15GENIChomozygous45374712
2040592494059250GA19GENICheterozygous45374713
2040594294059430AG17GENIChomozygous45374715
2040598164059817CT22GENIChomozygous45374716
2040600554060056CT16GENIChomozygous45374717
2040600994060100A-16GENICpossibly homozygous45374718
2040601404060141GC18GENICpossibly homozygous45374719
2040601774060178CT20GENIChomozygous45374720
2040602274060228TA25GENICpossibly homozygous45374721
2040603534060354CT28GENICpossibly homozygous45374722
2040608534060854CT8GENIChomozygous45374723