chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46563233765632338GA12GENIChomozygous112683482
46563310465633105CT16GENIChomozygous112683484
46563329365633294GC12GENIChomozygous112683486
46563534665635347TC14GENIChomozygous112683488
46563621565636216AG12GENIChomozygous112683490
46563784865637849AG8GENIChomozygous112683492
46564162365641624GA18GENIChomozygous112683496
46564180065641801CG12GENIChomozygous112683498
46564572165645722AG9GENIChomozygous112683500
46564697465646975AG10GENIChomozygous112683502
46564730965647310GA11GENICpossibly homozygous112683504
46564748665647487TG15GENIChomozygous112683506
46564894165648942GA10GENIChomozygous112683508
46564960665649607CT11GENIChomozygous112683510
46565171465651715TC7GENIChomozygous112683516
46565198465651985GA13GENIChomozygous112683518
46565258565652586AT8GENIChomozygous112683520
46565310765653108TC6GENIChomozygous112683522
46565361265653613AG9GENIChomozygous112683524
46565461365654614CT10GENIChomozygous112683526
46565469165654692TC9GENIChomozygous112683528
46565518265655183CT7GENIChomozygous112683530
46565632565656326GC8GENIChomozygous112683534
46566465165664652AG12GENIChomozygous112683546
46566779965667800TC5GENIChomozygous112683548
46567150865671509AT5GENIChomozygous112683550
46567480765674808TA7GENIChomozygous112683552
46567631065676311AG13GENIChomozygous112683554
46568338865683389CA12GENIChomozygous112683560
46568350165683502TC11GENIChomozygous112683562
46568352865683529GA10GENIChomozygous119277439
46568407065684071TG12GENIChomozygous112683564
46568445565684456AG7GENIChomozygous112683566
46568352965683530AG10GENIChomozygous113275611