chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1171827563171827564CA21GENICpossibly homozygous62271547
1171829725171829726TC8GENIChomozygous60943904
1171834193171834197TTTG----8GENIChomozygous61556144
1171836207171836208AT7GENICheterozygous60943928
1171836766171836767GGT4GENICheterozygous61309908
1171837160171837161CT7GENICpossibly homozygous61556146
1171840118171840119T-8GENIChomozygous60943944
1171840169171840170AG9GENIChomozygous61556147
1171843719171843720TA1GENIChomozygous60943948
1171845299171845300GA5GENICheterozygous60943951
1171847042171847046AAAC----3GENIChomozygous61556148
1171849685171849686AG6GENIChomozygous60943962
1171852805171852806CG12GENICpossibly homozygous61556152
1171853943171853944T-2GENIChomozygous61556153
1171854596171854597CA10GENICheterozygous60943975
1171855821171855822TC11GENIChomozygous60943981
1171856118171856119AG15GENICpossibly homozygous60943982
1171856406171856407AG6GENIChomozygous60943983
1171863276171863277CA17GENIChomozygous60943994
1171864693171864694G-2GENIChomozygous60943997
1171864994171864995AG6GENIChomozygous61556155