chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182491849324918494CA25GENIChomozygous110832114
182491926524919266CT26GENIChomozygous110832116
182491939224919393TC42GENICheterozygous119571782
182491939324919394TC42GENICheterozygous119571783
182491939624919397GA42GENICheterozygous119571784
182491940024919401GA45GENICheterozygous119571785
182491941524919416TC51GENICheterozygous119571786
182491944224919443TG29GENIChomozygous119571787
182491946124919462TC38GENICheterozygous119571788
182491946524919466AG39GENICheterozygous119485417
182491947624919477CG44GENICheterozygous119571789
182491948224919483TG49GENICheterozygous119485418
182491953424919535AG180GENICheterozygous119571790
182491954524919546CA183GENICheterozygous119571791
182491963724919638AC54GENICheterozygous119571792
182492091924920920AG37GENIChomozygous110832118
182492335824923359CT21GENIChomozygous110832120
182492361524923616AG34GENIChomozygous110647580
182492406924924070TG10GENIChomozygous110309508
182492061624920617AT12GENIChomozygous110812143
182492104624921047GA22GENIChomozygous110309500
182492130324921304GA25GENIChomozygous110309502
182492276324922764TA30GENIChomozygous110309504
182492321924923220TG30GENIChomozygous110309506
182492410024924101GA10GENIChomozygous110832122
182492499724924998CA28GENIChomozygous110832124
182492500824925009CT28GENIChomozygous110309510
182492530224925303CG21GENIChomozygous110832126
182492541424925415AG27GENIChomozygous110309512
182492572124925722AG26GENIChomozygous110309514
182492590324925904TG18GENIChomozygous110309516
182492613324926134CT28GENIChomozygous110309520
182492616424926165TC26GENIChomozygous110309522
182492650024926501CA7GENIChomozygous110832128
182492676724926768AG23GENIChomozygous110309528
182492740624927407GA12GENIChomozygous110309531
182492742724927428GA15GENIChomozygous110309533
182492749824927499AG17GENIChomozygous110309535
182492786524927866TC25GENIChomozygous110309538
182492813024928131AG23GENIChomozygous110309540