chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X11390081139009AG8GENIChomozygous140602059
X11396821139683CT10GENIChomozygous140602060
X11399741139975AG11GENIChomozygous140602061
X11404041140405GA14GENIChomozygous140602062
X11420961142097GA13GENIChomozygous140602063
X11436941143695AG8GENIChomozygous140602064
X11441911144192GA6GENIChomozygous140602065
X11455671145574AGACTCT14GENIChomozygous140574005
X11494861149487AG13GENIChomozygous140602066
X11501071150108A8GENICpossibly homozygous140574007
X11518551151856AG14GENIChomozygous140602067
X11552871155288GA16GENIChomozygous140602068
X11553981155398C15GENIChomozygous140574008
X11487421148743G11GENIChomozygous403473467
X11487421148743GT11GENICheterozygous403473468