chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
11440118814401189GA18GENIChomozygous62607452
11440192514401926TC22GENIChomozygous62607453
11440202014402021CT26GENIChomozygous62607454
11440219414402195A-15GENIChomozygous62607455
11440266414402665CT23GENIChomozygous62607456
11440299114402992T-19GENIChomozygous62444306
11440324714403248AG19GENIChomozygous60632464
11440355914403560TC17GENIChomozygous60632465
11440389314403894CCAA7GENICpossibly homozygous60632466
11440389314403894CCA7GENICheterozygous60632467
11440467914404680AG34GENIChomozygous62607457
11440488914404890TC17GENIChomozygous62607458
11440499714404998GA27GENIChomozygous62607459
11440544014405441TC16GENIChomozygous62607460
11440549214405493T-15GENIChomozygous62071924
11440550414405505AG15GENIChomozygous62607461
11440559014405591TC16GENIChomozygous62607462
11440572914405738AAACAAAAC---------3GENICheterozygous62607463
11440646814406469CT11GENIChomozygous62607464
11440685314406854TG25GENIChomozygous62607465
11440710714407108GGAA14GENIChomozygous62607466
11440712514407126T-21GENIChomozygous60632470
11440814514408149CTAA----26GENIChomozygous62607467
11440862414408625CT14GENIChomozygous62607468
11440877014408771AAT19GENIChomozygous60632471
11440962114409622TG31GENIChomozygous62607469
11440985814409859CT21GENIChomozygous62607470
11440985914409860AG20GENIChomozygous60632472
11440999814409999AG28GENIChomozygous62607471
11441025214410253TC30GENIChomozygous62607472
11441038414410385AG19GENIChomozygous60632474
11441055314410556AAT---1GENIChomozygous62252530
11441073814410739TC23GENIChomozygous60632477
11441116614411167GA17GENIChomozygous62607473
11441206114412062CCTTTTGGTTTTGGTTTTGGTTTTGGTTTTGG19GENIChomozygous62607474
11441218114412182CT28GENIChomozygous62607475
11441245214412453TC22GENIChomozygous60632482