chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2237031322370314AG31INTERGENIChomozygous810222629
X2237266122372662CT25INTERGENIChomozygous810222630
X2237587022375871TG20INTERGENIChomozygous810222631
X2237657522376576TC19INTERGENIChomozygous810222632
X2237846522378466CT15INTERGENIChomozygous810222633
X2237881522378816CT16INTERGENIChomozygous810222634
X2237961722379618TG23INTERGENIChomozygous810222635
X2237982222379823TA13INTERGENIChomozygous810222636
X2238001722380018CT19INTERGENIChomozygous810222637
X2238011022380111AG26INTERGENIChomozygous810222638
X2238015122380152GC21INTERGENIChomozygous810222639
X2238022922380230TG15INTERGENIChomozygous810222640
X2238087322380874TA15INTERGENIChomozygous810222641
X2238141622381417CT16INTERGENIChomozygous810222642
X2238148922381490CT15INTERGENIChomozygous810222643
X2238229822382299AT20INTERGENIChomozygous810222644
X2238254822382549GT8INTERGENIChomozygous810222645
X2238265522382656TC11INTERGENIChomozygous810222646
X2238317022383171AC6INTERGENIChomozygous810222647
X2238347022383471AT24INTERGENICpossibly homozygous810222648
X2238435222384353GA23INTERGENIChomozygous810222649
X2238436222384363AG22INTERGENIChomozygous810222650
X2238472922384730TC28INTERGENIChomozygous810222651
X2238521122385212AG24INTERGENIChomozygous810222652
X2238557922385580AG25INTERGENIChomozygous810222653
X2238798522387986CT27INTERGENIChomozygous810222654
X2238829822388299TC17INTERGENIChomozygous810222655
X2238838722388388TA14INTERGENIChomozygous810222656
X2238917122389172CT14INTERGENIChomozygous810222657
X2238927322389274GA18INTERGENIChomozygous810222658
X2239033722390338AG21INTERGENIChomozygous810222659
X2239119622391197TC26INTERGENIChomozygous810222660
X2239234722392348CT9INTERGENIChomozygous810222661
X2239565622395657TC18INTERGENIChomozygous810222662