chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109099123390991234T-15GENICpossibly homozygous51738494
109099185290991853CCACACAT2GENIChomozygous52397137
109099194490991945GA13GENIChomozygous51928503
109099277690992777GT22GENIChomozygous51928506
109099300390993004TC31GENIChomozygous51738500
109099352890993531CGG---27GENICheterozygous52397141
109099353490993539TTCCC-----26GENICheterozygous52397143
109099388690993887G-39GENICheterozygous51538804
109099403390994050CGCAGCAAGCAGGAGCT-----------------37GENICheterozygous51538808
109099460990994610GA11INTERGENICpossibly homozygous51928509
109099501690995017CT21INTERGENIChomozygous51738506
109099507490995076CA--18INTERGENIChomozygous51928512
109099553090995531CT20INTERGENIChomozygous51928519
109099575890995759GA28INTERGENIChomozygous51928522
109099598090995981AG29INTERGENIChomozygous51738510
109099631390996314TC31INTERGENIChomozygous51738512
109099714490997145GA16INTERGENIChomozygous52165962
109099726690997267TTTCTGGGGGTCAGCAGTG19INTERGENIChomozygous51928536
109099727290997273TC22INTERGENIChomozygous51928539
109099744190997442CT24INTERGENIChomozygous51928542
109099888190998884TGT---2INTERGENICheterozygous51738528
109099888890998889CCT2INTERGENICheterozygous53189545