chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2228504636228504637A-8GENIChomozygous59427451
2228504640228504641TC12GENICpossibly homozygous59427452
2228504686228504687TC19GENIChomozygous59427453
2228504691228504692T-18GENIChomozygous59427454
2228504946228504947TA12GENIChomozygous59427455
2228505170228505171TA12GENIChomozygous59427456
2228505272228505273TC8GENIChomozygous59427457
2228505292228505293AAT7GENIChomozygous59427458
2228505606228505607CT11GENIChomozygous59939338
2228505670228505671CT16GENIChomozygous59939339
2228506041228506042TC25GENIChomozygous59427459
2228506283228506299TTTGTTTGTTTGTTTG----------------4GENIChomozygous59427460
2228506325228506326TC12GENIChomozygous59427462
2228506491228506492CT19GENIChomozygous59427463
2228506503228506504CT16GENIChomozygous59427464
2228506548228506549CT8GENIChomozygous59427465
2228506621228506622AG18GENIChomozygous59427466
2228506779228506780GA37GENIChomozygous59939340
2228507182228507183AG21GENIChomozygous59427467
2228507496228507497CG25GENIChomozygous59427468
2228507944228507945CA36GENIChomozygous59939341
2228507947228507948TC36GENIChomozygous59427469
2228508507228508508TA24GENIChomozygous59427470
2228508825228508826GA16GENIChomozygous59427472
2228508827228508828GA16GENIChomozygous59427473
2228508897228508904GGGTTTA-------8GENIChomozygous59427474
2228509044228509045TG11GENICpossibly homozygous59939342
2228509084228509085CT15GENIChomozygous59427478
2228509255228509256AC32GENIChomozygous59427479
2228509321228509322TA36GENIChomozygous59427480
2228509339228509340TC33GENIChomozygous59427481
2228509520228509521CT29GENIChomozygous59939343
2228509594228509595GA19GENIChomozygous59427482
2228509664228509665CT17GENIChomozygous59427483