chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2237031322370314AG8GENIChomozygous956815046
X2237266122372662CT21GENIChomozygous956815047
X2237587022375871TG14GENIChomozygous956815048
X2237657522376576TC11GENIChomozygous956815049
X2237846522378466CT11GENIChomozygous956815050
X2237867322378674CT4GENIChomozygous956815051
X2237881522378816CT5GENIChomozygous956815052
X2237961722379618TG14GENIChomozygous956815053
X2237982222379823TA12GENICpossibly homozygous956815054
X2238011022380111AG7GENIChomozygous956815055
X2238087322380874TA14GENIChomozygous956815056
X2238141622381417CT6GENIChomozygous956815057
X2238148922381490CT8GENIChomozygous956815058
X2238229822382299AT8GENIChomozygous956815059
X2238347022383471AT10GENIChomozygous956815060
X2238435222384353GA15GENIChomozygous956815061
X2238436222384363AG16GENIChomozygous956815062
X2238472922384730TC6GENIChomozygous956815063
X2238521122385212AG10GENIChomozygous956815064
X2238557922385580AG14GENIChomozygous956815065
X2238798522387986CT6GENIChomozygous956815066
X2238829822388299TC10GENIChomozygous956815067
X2238838722388388TA12GENIChomozygous956815068
X2238917122389172CT7GENIChomozygous956815069
X2238927322389274GA14GENIChomozygous956815070
X2239033722390338AG21GENIChomozygous956815071