chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45545592555455926TTACAA4GENIChomozygous58076096
45545609555456096CCACGA13GENICpossibly homozygous58076098
45545641755456418CT14GENICpossibly homozygous58076100
45545659855456599AC3GENIChomozygous58076102
45545691155456912TC9GENIChomozygous57727519
45545780055457801GA15GENICpossibly homozygous58076104
45545908955459090AG18GENICheterozygous57727521
45545936055459361GA16GENIChomozygous58076106
45545964355459644AG19GENICpossibly homozygous57727525
45546052155460522CT13GENICpossibly homozygous57727529
45546083355460834TC8GENIChomozygous58076108
45546146555461466GA9GENICpossibly homozygous57727531
45546148755461488AG9GENICheterozygous57727533
45546151955461520TC5GENIChomozygous57727535
45546172555461726TC11GENIChomozygous57727539
45546185755461858CA7GENIChomozygous58076110
45546186555461866TA13GENIChomozygous58076112
45546227355462274GA13GENICpossibly homozygous58076113
45546244555462446CA9GENIChomozygous57727543
45546249455462495CT17GENIChomozygous57727545
45546271355462714CT4GENIChomozygous58076115
45546348455463485CT1GENIChomozygous57727547
45546447355464474GA21GENICpossibly homozygous57727551
45546456755464568GT17GENICpossibly homozygous57727553
45546476655464767CCCTT2GENIChomozygous57727555
45546520155465202GT7GENIChomozygous57727559
45546550855465509AG5GENIChomozygous57727561
45546556555465566TC10GENIChomozygous57727563
45546621355466214AG17GENIChomozygous57727565
45546622855466229CT10GENIChomozygous57727567
45546659055466591TA9GENIChomozygous57727571
45546686955466870TG12GENICpossibly homozygous57727573
45546692955466930GA10GENIChomozygous57727575
45546698555466986GA16GENIChomozygous57727577
45546707255467073AAT4GENICheterozygous57727579
45546723355467234GA21GENIChomozygous57727581