chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2237031322370314AG15INTERGENIChomozygous778224867
X2237266122372662CT26INTERGENIChomozygous778224868
X2237587022375871TG6INTERGENIChomozygous778224869
X2237657522376576TC9INTERGENIChomozygous778224870
X2237846522378466CT11INTERGENIChomozygous778224871
X2237867322378674CT16INTERGENIChomozygous778224872
X2237881522378816CT21INTERGENIChomozygous778224873
X2237961722379618TG20INTERGENIChomozygous778224874
X2237982222379823TA19INTERGENIChomozygous778224875
X2238001722380018CT14INTERGENIChomozygous778224876
X2238011022380111AG15INTERGENIChomozygous778224877
X2238015122380152GC15INTERGENICpossibly homozygous778224878
X2238022922380230TG14INTERGENIChomozygous778224879
X2238087322380874TA21INTERGENIChomozygous778224880
X2238141622381417CT22INTERGENIChomozygous778224881
X2238148922381490CT13INTERGENIChomozygous778224882
X2238229822382299AT14INTERGENIChomozygous778224883
X2238254822382549GT13INTERGENIChomozygous778224884
X2238265522382656TC9INTERGENIChomozygous778224885
X2238317022383171AC8INTERGENIChomozygous778224886
X2238347022383471AT18INTERGENIChomozygous778224887
X2238435222384353GA18INTERGENICpossibly homozygous778224888
X2238436222384363AG19INTERGENIChomozygous778224889
X2238472922384730TC26INTERGENIChomozygous778224890
X2238521122385212AG27INTERGENIChomozygous778224891
X2238557922385580AG34INTERGENIChomozygous778224892
X2238798522387986CT10INTERGENIChomozygous778224893
X2238829822388299TC7INTERGENIChomozygous778224894
X2238838722388388TA10INTERGENIChomozygous778224895
X2238917122389172CT21INTERGENIChomozygous778224896
X2238927322389274GA15INTERGENIChomozygous778224897
X2239033722390338AG24INTERGENICpossibly homozygous778224898
X2239119622391197TC19INTERGENIChomozygous778224899
X2239565622395657TC16INTERGENIChomozygous778224900