chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
63610810736108108TTCTC7GENIChomozygous54353114
63610838336108384TG4GENIChomozygous54353116
63610964636109647TG8GENIChomozygous54353118
63611104636111047GA21GENIChomozygous54353122
63611299936113000GA21GENICpossibly homozygous54353126
63611406636114067CT4GENIChomozygous54353128
63611520036115201CT11GENIChomozygous54353134
63611521336115214AC11GENIChomozygous54353136
63611645136116452GA15GENIChomozygous54353138
63611657136116572TC22GENIChomozygous54353140
63611778036117781AG29GENICpossibly homozygous54353142
63612294436122945CT17GENICheterozygous54353144
63612536636125367AT15GENICpossibly homozygous54353150
63612815636128160ACAC----8GENICpossibly homozygous54353160
63613248536132486GA11GENIChomozygous54353164
63613355436133555AG14GENIChomozygous54353166
63613368636133687AG18GENICpossibly homozygous54353168
63613474136134742GT7GENIChomozygous54353170
63613493236134933GA4GENIChomozygous54353174
63613498336134984AG7GENIChomozygous54353176
63613695436136955TA28GENICpossibly homozygous54353180
63613741336137414CT3GENIChomozygous54353182
63613743336137434GGA3GENICheterozygous54353184
63612808536128086TTACAC2GENICheterozygous55493776