chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71171458811714589CT21GENIChomozygous115568906
71171817311718174GA6GENIChomozygous115568909
71171820011718201GC7GENIChomozygous115568910
71171824611718247GC7GENIChomozygous115568911
71171825711718258CT11GENIChomozygous115568912
71171931511719316TC10GENIChomozygous115568913
71172005411720055AT9GENIChomozygous115568914
71172008111720082GT12GENIChomozygous115568915
71172093911720940CT25GENIChomozygous115568916
71172110911721110GA10GENIChomozygous115568917
71172118511721186AG10GENIChomozygous115568918
71172141011721411GT13GENIChomozygous115568919
71172293211722933TG10GENIChomozygous115568920
71172343611723437AC15GENICheterozygous118389140
71172374911723750AG11GENIChomozygous115568921
71172405711724058CT3GENIChomozygous115568922
71172413711724138TC2GENIChomozygous115568923
71172426111724262TC4GENIChomozygous115568924