chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14762124947621250AG13GENICpossibly homozygous60697861
14762557747625578AATTTT1GENIChomozygous60697862
14762735147627352CT18GENIChomozygous60697863
14762784547627846CA13GENICpossibly homozygous60697864
14762784647627847AG10GENICpossibly homozygous60697865
14762816547628166TC15GENIChomozygous60697866
14763024147630242AG13GENICpossibly homozygous60697869
14763216747632168TC13GENICheterozygous60697870
14763359947633600TC17GENIChomozygous60697873
14763430047634301GA6GENICheterozygous60697874
14763524447635246CA--8GENICpossibly homozygous61666152
14763840547638406AG18GENIChomozygous60697876
14764060447640606AC--3GENIChomozygous60697878
14764112447641125TTAC3GENICheterozygous60697880
14764112447641125TTACACAC3GENICheterozygous61410419
14764117547641176CCGTGTGTGT2GENICheterozygous62074814
14764171747641719GG--2GENIChomozygous60697882