chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
51681002416810025CT3GENICheterozygous131857649
51681032316810324GA4GENIChomozygous132304341
51681035316810354CT3GENIChomozygous132304342
51681532316815324AG9GENICheterozygous128280689
51681514616815147CT2GENIChomozygous130553368
51681187016811871CA3GENICheterozygous133823178
51681535016815351GT12GENICheterozygous130758003
51682248916822490CA18GENIChomozygous113675060
51682323816823239CT20GENIChomozygous113675067
51682525316825254CG29GENIChomozygous118870634
51682162016821621CT19GENIChomozygous118870626
51682229116822292AT14GENIChomozygous118870628
51682263216822633CA16GENIChomozygous118870630
51682368416823685GA16GENIChomozygous118870632
51682558516825586GA15GENIChomozygous118870636
51682597916825980GA16GENIChomozygous113675079
51682618916826189T12GENIChomozygous128154534
51682631616826317GA20GENIChomozygous113675081
51682644116826442GA19GENIChomozygous113675083
51682689216826893AG20GENIChomozygous113675087
51682829716828298TC36GENIChomozygous113675091
51682883816828839CG20GENIChomozygous118870638
51682977616829777GT19GENIChomozygous113675099
51683036116830362GA17GENIChomozygous113675105
51683073516830736GA23GENIChomozygous118870640
51683074416830745GT26GENIChomozygous118870642
51683107016831071AG22GENIChomozygous113675111
51683285616832857AC27GENICpossibly homozygous118870644
51683305416833055TC18GENIChomozygous113675149
51683323616833237GA23GENIChomozygous113675151
51683372716833728AT13GENICheterozygous122248099
51683372916833730AT14GENICheterozygous132400845
51683373116833732AT14GENICheterozygous132400846
51683509016835091CT31GENIChomozygous113675153
51683607016836071AG20GENIChomozygous113675157
51683698816836989TC28GENIChomozygous113675159
51683772316837724AT25GENIChomozygous113675161
51683898116838982CT24GENIChomozygous114473168
51683980016839801GT27GENICpossibly homozygous113675163
51683981316839814CT28GENICpossibly homozygous118870646
51683024016830251CCCTGACCTCT22GENIChomozygous131853209