chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116671397266713973GA18GENIChomozygous890311075
116671480766714808CT9GENIChomozygous890311076
116671589766715898GA20GENIChomozygous890311077
116671617466716175CT22GENIChomozygous890311078
116671627766716278TC21GENIChomozygous890311079
116671643566716436CG20GENIChomozygous890311080
116671647966716480TC12GENIChomozygous890311081
116671668466716685GA8GENIChomozygous890311082
116671751166717512CG6GENIChomozygous890311083
116671760366717604GC16GENIChomozygous890311084
116671771366717714GA6GENIChomozygous890311085
116671894366718944AG15GENIChomozygous890311086
116672030466720305GA10GENIChomozygous890311087
116672098466720985TA4GENIChomozygous890311088
116672255866722559GT23GENIChomozygous890311089
116672349766723498GC11GENIChomozygous890311090
116672350966723510TC10GENIChomozygous890311091
116672411266724113AC19GENIChomozygous890311092
116672422866724229TC12GENIChomozygous890311093
116672543466725435TC13GENIChomozygous890311094
116672636166726362TC9GENIChomozygous890311095
116672675466726755GC10GENIChomozygous890311096
116672886966728870CA4GENICheterozygous890311097
116673084166730842GA9GENIChomozygous890311098
116673086466730865GA15GENIChomozygous890311099