chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108697244886972449AG3GENIChomozygous69378769
108697385286973853AG19GENIChomozygous68143764
108697873786978738GA9GENIChomozygous68143776
108697934486979345CT21GENIChomozygous68143779
108698003386980034CT9GENIChomozygous68143782
108698360186983602CT6GENIChomozygous68143791
108698423386984234AG11GENIChomozygous68143794
108698464686984647TC15GENIChomozygous68143797
108698489886984899CT10GENIChomozygous68143803
108698499586984996AC8GENIChomozygous68143806
108698946186989462CG17GENIChomozygous68143812
108699054186990542GT7GENIChomozygous68143824
108699081786990818CT12GENIChomozygous68143827
108699190386991904CT11GENIChomozygous68143830
108699193786991938GA10GENIChomozygous68143833
108699389986993900TC17GENIChomozygous68143836
108699592686995927AC13GENIChomozygous68143844
108697967986979680TG5GENIChomozygous69436591
108699364786993647TTA6GENIChomozygous69436593
108699226286992266TTAT3GENIChomozygous69274129
108699286786992868T10GENICheterozygous69274136
108699618186996182TC7GENIChomozygous68143856
108699642086996421GT6GENIChomozygous69436595
108699642486996425TG3GENIChomozygous69436597
108699656686996567GA10GENIChomozygous68143859
108699989786999898A21GENICheterozygous69274140
108700077187000772A16GENICheterozygous69274144
108700084287000843CT18GENIChomozygous68143862
108700088987000890AG12GENIChomozygous68143865
108700609187006092AG15GENIChomozygous68143871
108700665687006656GTTGTGT12GENICheterozygous69436599
108701172987011730AG23GENIChomozygous68143877
108701185487011855CT21GENIChomozygous68143880
108701724587017246GA21GENIChomozygous68143886
108701760587017606CT9GENIChomozygous68143889
108702070187020702GT18GENIChomozygous68143892
108702468887024689GA6GENIChomozygous68143901
108702725887027259C19GENICheterozygous69274151
108702772487027725CT9GENIChomozygous68143904