chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7144869376144869377CA32GENICheterozygous115945969
7144869686144869687GA24GENICheterozygous115945971
7144870150144870151T13GENIChomozygous128532154
7144870187144870187G19GENIChomozygous128532155
7144870203144870203G19GENIChomozygous128532156
7144870219144870219G21GENIChomozygous128532157
7144870245144870245T20GENIChomozygous128532158
7144870280144870281TC22GENIChomozygous116101369
7144870284144870284A21GENIChomozygous128532159
7144870311144870312A15GENIChomozygous128532160
7144870316144870317AC15GENIChomozygous118339331
7144870323144870323TA14GENIChomozygous128532161
7144870361144870361AG6GENIChomozygous128532166
7144870331144870332C11GENIChomozygous128532162
7144870334144870335G11GENIChomozygous128532163
7144870352144870353G7GENIChomozygous128532164
7144870358144870359T7GENIChomozygous128532165
7144870279144870280CT22GENIChomozygous118261255
7144870373144870374GT5GENIChomozygous115945972
7144870414144870415A10GENIChomozygous128532167
7144870417144870418G10GENIChomozygous128532168
7144870434144870434G9GENIChomozygous128532169
7144870438144870439T9GENIChomozygous128532170
7144870450144870451C8GENIChomozygous128532171
7144870459144870460T7GENIChomozygous128532172
7144870474144870475T7GENIChomozygous128532173
7144870484144870485GA8GENIChomozygous118332851
7144870485144870486AG8GENIChomozygous118332853
7144870495144870495G9GENIChomozygous128532174
7144870523144870524T12GENIChomozygous128532175
7144870541144870542GT14GENIChomozygous115945974
7144870546144870546T14GENIChomozygous128532176
7144870550144870550G15GENIChomozygous128532177
7144870569144870569G18GENIChomozygous128532178
7144870578144870579G19GENIChomozygous128532179
7144870591144870591A19GENIChomozygous128532180