chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
11440264014402641TA26GENIChomozygous60632463
11440324714403248AG31GENIChomozygous60632464
11440355914403560TC32GENIChomozygous60632465
11440389314403894CCAA13GENICheterozygous60632466
11440389314403894CCA13GENICheterozygous60632467
11440570714405708TTAAAAC6GENIChomozygous60632468
11440647814406479A-29GENICpossibly homozygous60632469
11440712514407126T-21GENIChomozygous60632470
11440877014408771AAT13GENIChomozygous60632471
11440985914409860AG27GENIChomozygous60632472
11441033914410340AT14GENIChomozygous60632473
11441038414410385AG12GENIChomozygous60632474
11441054714410556AATAATAAT---------6GENICheterozygous62323230
11441055014410556AATAAT------6GENICheterozygous62120123
11441073814410739TC22GENIChomozygous60632477
11441149814411502CCTT----38GENIChomozygous60632478
11441167814411679AC31GENIChomozygous60632479
11441206114412062CCTTTTGGTTTTGG11GENIChomozygous60632480
11441236014412361AT33GENIChomozygous60632481
11441245214412453TC26GENIChomozygous60632482
11441296514412966AT26GENIChomozygous60632483
11441310314413104TTAC24GENIChomozygous60632484
11441333814413339GT32GENIChomozygous60632485
11441411314414114AC32GENIChomozygous60632486