chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71171269811712699GA16GENIChomozygous116003649
71171458811714589CT20GENIChomozygous115568906
71171817311718174GA14GENIChomozygous115568909
71171820011718201GC24GENIChomozygous115568910
71171824611718247GC10GENIChomozygous115568911
71171825711718258CT10GENIChomozygous115568912
71171931511719316TC9GENIChomozygous115568913
71172005411720055AT20GENICheterozygous115568914
71172008111720082GT9GENIChomozygous115568915
71172093911720940CT27GENIChomozygous115568916
71172110911721110GA12GENIChomozygous115568917
71172118511721186AG26GENIChomozygous115568918
71172141011721411GT25GENIChomozygous115568919
71172293211722933TG19GENIChomozygous115568920
71172348511723486CA6GENIChomozygous116003650
71172374911723750AG12GENIChomozygous115568921
71172405711724058CT14GENIChomozygous115568922
71172413711724138TC12GENIChomozygous115568923
71172426111724262TC18GENIChomozygous115568924