chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104325087743250878CCT9GENICpossibly homozygous52371934
104325088043250881T-9GENICheterozygous52722379
104325097743250981CTTA----26GENIChomozygous52147500
104325105443251055GA20GENIChomozygous52317294
104325234043252341TC34GENIChomozygous52147502
104325317143253177TTTTTT------4GENICheterozygous52371936
104325105143251054TTC---21GENIChomozygous52190870
104325213943252140AAAGG17GENIChomozygous52190872
104325226243252263TC20GENIChomozygous52190874
104325269043252691C-30GENIChomozygous51435069