chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7124339161124339162GC31GENIChomozygous115865589
7124339853124339854CT29GENIChomozygous115865591
7124340150124340151TC26GENIChomozygous116226616
7124341609124341610CA24GENICpossibly homozygous116410126
7124344290124344291CA32GENIChomozygous115865605
7124344725124344726AG19GENIChomozygous116226622
7124346017124346018AG26GENIChomozygous115865615
7124351265124351266AG22GENIChomozygous115865627
7124354543124354544TC31GENIChomozygous115865633
7124356107124356108GA19GENIChomozygous116410127
7124357590124357591CT21GENIChomozygous115865637
7124360113124360114CT14GENIChomozygous116410128
7124361076124361077AG26GENIChomozygous116410129
7124361238124361239CT25GENIChomozygous116410130
7124361846124361847GA37GENIChomozygous116410131
7124366145124366146TC29GENIChomozygous115865653
7124351259124351260TG28GENIChomozygous118259334
7124351260124351261GC28GENIChomozygous118259336