chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2040548044054805TTTTTTG29GENIChomozygous45374702
2040548054054806TTTTTG29GENIChomozygous45374703
2040548084054809TTG29GENICpossibly homozygous45374704
2040551524055153CCAA49GENIChomozygous45374705
2040557234055724CT32GENICpossibly homozygous45374706
2040563084056309TC40GENICpossibly homozygous45374707
2040568814056882AG46GENIChomozygous45374708
2040574564057457AC36GENICheterozygous45374709
2040583464058347GA39GENICpossibly homozygous45374710
2040585854058586CT29GENIChomozygous45374711
2040591054059106CT52GENIChomozygous45374712
2040592494059250GA66GENIChomozygous45374713
2040593514059352AATGTGTGTGTGTG17GENIChomozygous45374714
2040594294059430AG50GENICpossibly homozygous45374715
2040598164059817CT46GENIChomozygous45374716
2040600554060056CT65GENIChomozygous45374717
2040600994060100A-57GENIChomozygous45374718
2040601404060141GC64GENIChomozygous45374719
2040601774060178CT63GENICpossibly homozygous45374720
2040602274060228TA56GENIChomozygous45374721
2040603534060354CT60GENIChomozygous45374722
2040608534060854CT33GENICpossibly homozygous45374723