chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46563233765632338GA5GENIChomozygous112683482
46563310465633105CT21GENIChomozygous112683484
46563329365633294GC21GENIChomozygous112683486
46563534665635347TC19GENIChomozygous112683488
46563621565636216AG22GENIChomozygous112683490
46563784865637849AG18GENIChomozygous112683492
46564103665641037CT25GENIChomozygous112683494
46564162365641624GA22GENIChomozygous112683496
46564180065641801CG25GENIChomozygous112683498
46564572165645722AG23GENIChomozygous112683500
46564654365646544CT28GENICpossibly homozygous113346434
46564697465646975AG18GENICpossibly homozygous112683502
46564730965647310GA23GENIChomozygous112683504
46564748665647487TG23GENIChomozygous112683506
46564894165648942GA17GENIChomozygous112683508
46564960665649607CT27GENIChomozygous112683510
46565099565650996AG46GENICheterozygous112683512
46565103565651036AG70GENICheterozygous112683514
46565107465651075GA51GENICheterozygous113030588
46565171465651715TC35GENIChomozygous112683516
46565198465651985GA34GENIChomozygous112683518
46565258565652586AT30GENIChomozygous112683520
46565310765653108TC19GENIChomozygous112683522
46565361265653613AG35GENIChomozygous112683524
46565461365654614CT15GENIChomozygous112683526
46565469165654692TC14GENIChomozygous112683528
46565518265655183CT21GENIChomozygous112683530
46565632565656326GC13GENIChomozygous112683534
46565705965657060TC4GENICheterozygous112683536
46565708165657082CT8GENICheterozygous112683542
46566465165664652AG11GENIChomozygous112683546
46566779965667800TC12GENIChomozygous112683548
46567150865671509AT16GENIChomozygous112683550
46567480765674808TA13GENIChomozygous112683552
46567631065676311AG16GENIChomozygous112683554
46567654365676544CT23GENIChomozygous112683556
46567731065677311AG15GENICpossibly homozygous113030590
46568338865683389CA21GENIChomozygous112683560
46568350165683502TC38GENIChomozygous112683562
46568445565684456AG29GENIChomozygous112683566