chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
11440264014402641TA70GENIChomozygous60632463
11440324714403248AG63GENIChomozygous60632464
11440355914403560TC64GENIChomozygous60632465
11440389314403894CCAA14GENICheterozygous60632466
11440389314403894CCA14GENICheterozygous60632467
11440570714405708TTAAAAC11GENIChomozygous60632468
11440647814406479A-50GENIChomozygous60632469
11440712514407126T-66GENIChomozygous60632470
11440877014408771AAT48GENIChomozygous60632471
11440985914409860AG77GENIChomozygous60632472
11441033914410340AT56GENIChomozygous60632473
11441038414410385AG51GENIChomozygous60632474
11441053814410544AATAAT------14GENIChomozygous60632475
11441073814410739TC51GENIChomozygous60632477
11441149814411502CCTT----55GENIChomozygous60632478
11441167814411679AC77GENIChomozygous60632479
11441206114412062CCTTTTGGTTTTGG11GENIChomozygous60632480
11441236014412361AT76GENIChomozygous60632481
11441245214412453TC61GENIChomozygous60632482
11441296514412966AT55GENIChomozygous60632483
11441310314413104TTAC42GENICpossibly homozygous60632484
11441333814413339GT69GENIChomozygous60632485
11441411314414114AC68GENIChomozygous60632486