chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------8GENIChomozygous712502047
85378107053781071CT12GENIChomozygous570618861
85378121053781211AG11GENIChomozygous570618862
85378128753781288GGA10GENICheterozygous712502049
85378128753781288GGAA10GENICheterozygous712502050
85378128753781288GGAAA10GENICheterozygous712502051
85378133353781334AG16GENIChomozygous570618863
85378146653781467AG11GENIChomozygous570618864
85378180553781806AG18GENIChomozygous570618865
85378193153781932TTTA12GENICheterozygous712502052
85378193153781932TTTTA12GENICheterozygous712502053
85378200853782013GTTTG-----16GENIChomozygous712502055
85378241353782414CT12GENIChomozygous570618866
85378260753782608TC16GENIChomozygous570618867
85378277053782771GA7GENIChomozygous570618868
85378331953783320AG15GENIChomozygous570618869
85378340253783403T-8GENICpossibly homozygous712502056
85378373853783739GT23GENIChomozygous570618870
85378379353783794TC15GENIChomozygous570618871
85378391753783918T-5GENIChomozygous712502057
85378391953783926TGCGTGT-------6GENIChomozygous712502058
85378404853784049TC23GENIChomozygous570618872
85378438353784384A-17GENIChomozygous712502059
85378550753785508TTTTTTTC6GENIChomozygous712502060