chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
53962057239620589GGCAAATTCGAACGTTC10GENICpossibly homozygous128172129
53962087839620879AT11GENIChomozygous119152477
53962157039621571CT13GENIChomozygous113758357
53962396439623965AG14GENIChomozygous119152479
53962563039625631A15GENIChomozygous128172130
53962563639625636T15GENIChomozygous128172131
53962564939625649G14GENIChomozygous128172132
53962569439625695T14GENIChomozygous128172133
53962569939625699A14GENIChomozygous128172134
53962571039625710C16GENIChomozygous128172135
53962785339627854GA25GENIChomozygous119152481
53962828139628282TC9GENIChomozygous119152483
53962844439628445C17GENIChomozygous128172136
53962971539629715T3GENIChomozygous128172137
53963066139630662GA15GENIChomozygous119152485
53963325939633260CT23GENIChomozygous119152487
53963343939633440CA21GENIChomozygous119152489
53963363339633634GA14GENIChomozygous119152492
53963383039633830TA6GENIChomozygous128172148
53963473239634733AG29GENIChomozygous119152494
53963538039635381TA28GENIChomozygous119152496
53963544939635450CA25GENIChomozygous119152498
53963616739636168AG14GENIChomozygous119152500
53963672139636722CG19GENIChomozygous119152502
53963773739637737A17GENIChomozygous128172150
53963935139639352AT26GENIChomozygous119152504
53963985839639859CG21GENIChomozygous119152506
53964126039641264GTGC15GENIChomozygous131381705
53964387439643875A15GENICpossibly homozygous128172151
53964658139646582CT20GENIChomozygous119152508
53964664139646642TC20GENIChomozygous119152510
53964694439646945GA22GENIChomozygous119152512
53964908039649081GA20GENIChomozygous113758381
53965012739650128AT25GENIChomozygous119152514
53965042939650431AA13GENIChomozygous128172153
53965045439650455AG13GENIChomozygous113758385
53965063539650636AG11GENIChomozygous113758387
53965066839650669GC14GENIChomozygous113758389
53965085039650851CT10GENIChomozygous113758391