chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2233603125233603126CG20GENIChomozygous110310887
2233603203233603204GC16GENIChomozygous110310889
2233603310233603311CT23GENIChomozygous110310891
2233603332233603333CA23GENIChomozygous110310893
2233603349233603350CG24GENIChomozygous110310895
2233603393233603394AG25GENIChomozygous110310897
2233604448233604449AG15GENIChomozygous110310899
2233605147233605148GC14GENIChomozygous110310901
2233606872233606873TA15GENIChomozygous110310903
2233607870233607871CT15GENIChomozygous110310905
2233608554233608555GT16GENIChomozygous110310907
2233608580233608581GA15GENIChomozygous110310909
2233608593233608594CG15GENICpossibly homozygous110310911
2233610088233610089CT16GENIChomozygous110310915
2233605132233605132A13GENIChomozygous127749297
2233605784233605784G12GENIChomozygous127749298
2233606118233606119C16GENIChomozygous127749299
2233610711233610711G10GENIChomozygous127749300
2233612250233612251GA8GENIChomozygous110310917
2233613195233613196AG17GENIChomozygous110310919
2233613635233613636GT18GENICpossibly homozygous110310921
2233613661233613662CG16GENIChomozygous110310923
2233614053233614053C14GENIChomozygous127749301
2233614061233614062CA14GENIChomozygous110310925
2233615830233615831CT18GENIChomozygous110310927
2233616021233616022AG20GENIChomozygous110310929
2233617390233617391AG19GENIChomozygous110310931
2233617474233617475GA26GENIChomozygous110310933
2233612178233612179T3GENIChomozygous129870817