chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118405205384052054AG29GENIChomozygous116069109
118405205584052056GA29GENIChomozygous116069111
118405218684052187AG28GENICpossibly homozygous116069113
118405600684056007GT20GENIChomozygous116069115
118405647184056472CT30GENIChomozygous116069117
118405743884057439GT25GENIChomozygous116069119
118405900584059006AG15GENIChomozygous116069121
118405926884059269GA18GENIChomozygous116069123
118405934084059341GA16GENIChomozygous116069125
118406000984060010AG19GENIChomozygous116069127
118406022284060223CA18GENIChomozygous116069129
118406126484061265GA16GENIChomozygous116069131
118406192184061922GA19GENIChomozygous116069133
118406264984062650AG21GENIChomozygous116069135
118406266884062669CA18GENIChomozygous116069137
118406282384062824AC12GENIChomozygous116069139
118406297984062980CT14GENIChomozygous116069141
118406357884063579AG18GENIChomozygous116069143
118406540584065406CT28GENIChomozygous116069145
118406561084065611TC20GENIChomozygous116069147
118406640884066409CT19GENIChomozygous116069149
118406708084067081AG9GENIChomozygous116069151
118406739884067399AT10GENIChomozygous116069153