chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91704170217041703CT11GENIChomozygous117270068
91704673217046733AG19GENIChomozygous117270069
91704770517047706CT25GENIChomozygous117270070
91704864617048647TA17GENIChomozygous117270071
91704869417048695TA20GENIChomozygous117270072
91705193417051935TG3GENICheterozygous126497861
91705217617052177GA22GENIChomozygous117270076
91705235317052354TC16GENIChomozygous117270077
91705263617052637GT15GENIChomozygous117270078
91705737217057373GA14GENIChomozygous117270079
91705757017057571AC14GENIChomozygous117270080
91705896917058970GA14GENIChomozygous117270082
91705898617058987AG8GENIChomozygous117270083