chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
51681555516815556TG15GENICheterozygous129919692
51681613616816137CT17GENICheterozygous128280692
51681614516816146GA19GENICheterozygous128280693
51681621016816211CT16GENICheterozygous128280694
51682162016821621CT17GENIChomozygous118870626
51682229116822292AT27GENIChomozygous118870628
51682248916822490CA19GENIChomozygous113675060
51682263216822633CA26GENIChomozygous118870630
51682323816823239CT24GENIChomozygous113675067
51682368416823685GA14GENIChomozygous118870632
51682525316825254CG20GENIChomozygous118870634
51682558516825586GA15GENIChomozygous118870636
51682597916825980GA16GENIChomozygous113675079
51682618916826189T12GENIChomozygous128154534
51682631616826317GA21GENIChomozygous113675081
51682644116826442GA18GENIChomozygous113675083
51682689216826893AG16GENIChomozygous113675087
51682829716828298TC18GENIChomozygous113675091
51682883816828839CG23GENIChomozygous118870638
51682977616829777GT19GENIChomozygous113675099
51683036116830362GA30GENIChomozygous113675105
51683073516830736GA23GENIChomozygous118870640
51683074416830745GT22GENIChomozygous118870642
51683107016831071AG14GENIChomozygous113675111
51683285616832857AC15GENIChomozygous118870644
51683305416833055TC16GENIChomozygous113675149
51683323616833237GA17GENIChomozygous113675151
51683509016835091CT32GENIChomozygous113675153
51683607016836071AG22GENIChomozygous113675157
51683698816836989TC12GENIChomozygous113675159
51683772316837724AT17GENIChomozygous113675161
51683898116838982CT18GENIChomozygous114473168
51683980016839801GT24GENIChomozygous113675163
51683981316839814CT28GENIChomozygous118870646
51683024016830251CCCTGACCTCT29GENIChomozygous131853209