chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109099123390991234T-18GENICpossibly homozygous51738494
109099185290991853CCACAT7GENICheterozygous52968326
109099194490991945GA17GENIChomozygous51928503
109099277690992777GT25GENIChomozygous51928506
109099300390993004TC22GENIChomozygous51738500
109099388690993887G-26GENICheterozygous51538804
109099403390994050CGCAGCAAGCAGGAGCT-----------------26GENICheterozygous51538808
109099441290994413TTC11GENICheterozygous52397145
109099185290991853CCACACAT7GENICheterozygous52397137
109099352890993531CGG---26GENICheterozygous52397141
109099353490993539TTCCC-----25GENICheterozygous52397143
109099460990994610GA16INTERGENIChomozygous51928509
109099501690995017CT18INTERGENIChomozygous51738506
109099507290995076CACA----19INTERGENICheterozygous51738508
109099507490995076CA--19INTERGENICpossibly homozygous51928512
109099553090995531CT17INTERGENIChomozygous51928519
109099575890995759GA22INTERGENIChomozygous51928522
109099598090995981AG29INTERGENIChomozygous51738510
109099631390996314TC23INTERGENIChomozygous51738512
109099714490997145GA23INTERGENIChomozygous52165962
109099726690997267TTTCTGGGGGTCAGCAGTG17INTERGENIChomozygous51928536
109099727290997273TC19INTERGENIChomozygous51928539
109099744190997442CT23INTERGENIChomozygous51928542