chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109099123390991234T-16GENICpossibly homozygous51738494
109099300390993004TC24GENIChomozygous51738500
109099388690993887G-52GENICheterozygous51538804
109099403390994050CGCAGCAAGCAGGAGCT-----------------56GENICheterozygous51538808
109099460990994610GA25INTERGENIChomozygous51928509
109099194490991945GA21GENIChomozygous51928503
109099277690992777GT29GENIChomozygous51928506
109099185290991853CCACACAT8GENICheterozygous52397137
109099352890993531CGG---47GENICheterozygous52397141
109099353490993539TTCCC-----48GENICheterozygous52397143
109099441290994413TTC32GENICheterozygous52397145
109099185290991853CCACAT8GENICheterozygous52968326
109099501690995017CT29INTERGENIChomozygous51738506
109099507490995076CA--24INTERGENIChomozygous51928512
109099553090995531CT22INTERGENIChomozygous51928519
109099575890995759GA28INTERGENIChomozygous51928522
109099598090995981AG25INTERGENIChomozygous51738510
109099631390996314TC30INTERGENIChomozygous51738512
109099714490997145GA29INTERGENIChomozygous52165962
109099726690997267TTTCTGGGGGTCAGCAGTG21INTERGENIChomozygous51928536
109099727290997273TC23INTERGENIChomozygous51928539
109099744190997442CT40INTERGENIChomozygous51928542