chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2233605147233605148GC21GENIChomozygous110310901
2233607537233607538CA16GENIChomozygous110837632
2233607870233607871CT15GENIChomozygous110310905
2233608593233608594CG14GENIChomozygous110310911
2233609230233609231TA10GENIChomozygous110310913
2233609391233609392AT16GENIChomozygous110837633
2233610088233610089CT26GENIChomozygous110310915
2233611890233611891CA27GENICpossibly homozygous110629454
2233612250233612251GA25GENIChomozygous110310917
2233612761233612762AT26GENICpossibly homozygous110837635
2233613635233613636GT22GENIChomozygous110310921
2233613661233613662CG30GENIChomozygous110310923
2233616021233616022AG11GENIChomozygous110310929
2233617390233617391AG17GENIChomozygous110310931
2233617474233617475GA11GENIChomozygous110310933
2233618392233618393GT21GENIChomozygous110837637
2233618517233618518AT25GENIChomozygous110837639
2233618998233618999CT11GENIChomozygous110837641
2233619615233619616GA17GENIChomozygous110837643
2233619625233619626TC20GENIChomozygous110837645