chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2040548044054805TTTTTTG23GENIChomozygous45374702
2040548054054806TTTTTG23GENIChomozygous45374703
2040548084054809TTG23GENICpossibly homozygous45374704
2040551524055153CCAA18GENIChomozygous45374705
2040557234055724CT22GENICpossibly homozygous45374706
2040563084056309TC25GENIChomozygous45374707
2040568814056882AG30GENIChomozygous45374708
2040574564057457AC22GENICheterozygous45374709
2040583464058347GA25GENIChomozygous45374710
2040585854058586CT16GENIChomozygous45374711
2040591054059106CT18GENIChomozygous45374712
2040592494059250GA23GENIChomozygous45374713
2040593514059352AATGTGTGTGTGTG7GENIChomozygous45374714
2040594294059430AG15GENIChomozygous45374715
2040598164059817CT27GENIChomozygous45374716
2040600554060056CT23GENIChomozygous45374717
2040600994060100A-18GENIChomozygous45374718
2040601404060141GC16GENIChomozygous45374719
2040601774060178CT21GENIChomozygous45374720
2040602274060228TA25GENIChomozygous45374721
2040603534060354CT23GENIChomozygous45374722
2040608534060854CT11GENIChomozygous45374723