chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
155750581857505818GG13GENIChomozygous129259501
155750582157505821GG12GENIChomozygous129259502
155750582957505829A12GENIChomozygous129259503
155750583357505833G15GENIChomozygous129259504
155750584757505847G16GENIChomozygous129259505
155750585757505858TG19GENIChomozygous112809314
155750587357505873AG17GENIChomozygous129259506
155750587557505875G19GENIChomozygous129259507
155750587757505878G20GENIChomozygous129259508
155750590257505902G24GENIChomozygous129259509
155750592557505925A28GENIChomozygous129259510
155750596157505961T36GENIChomozygous131519747
155752120757521208C15GENICpossibly homozygous130592751
155750596957505970C36GENIChomozygous131519748
155750597957505979G34GENIChomozygous131519749