chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7144865735144865736AG16GENIChomozygous115945964
7144866560144866561TC32GENIChomozygous115945966
7144869078144869079AG32GENIChomozygous115945967
7144869376144869377CA41GENICheterozygous115945969
7144869686144869687GA32GENICheterozygous115945971
7144870150144870151T23GENIChomozygous128532154
7144870187144870187G24GENIChomozygous128532155
7144870203144870203G27GENIChomozygous128532156
7144870219144870219G28GENIChomozygous128532157
7144870245144870245T24GENIChomozygous128532158
7144870280144870281TC20GENIChomozygous116101369
7144870284144870284A20GENIChomozygous128532159
7144870311144870312A16GENIChomozygous128532160
7144870316144870317AC16GENIChomozygous118339331
7144870323144870323TA16GENIChomozygous128532161
7144870331144870332C15GENIChomozygous128532162
7144870334144870335G14GENIChomozygous128532163
7144870352144870353G10GENIChomozygous128532164
7144870358144870359T9GENIChomozygous128532165
7144870361144870361AG8GENIChomozygous128532166
7144870373144870374GT5GENIChomozygous115945972
7144870414144870415A19GENIChomozygous128532167
7144870417144870418G20GENIChomozygous128532168
7144870434144870434G17GENICpossibly homozygous128532169
7144870438144870439T15GENIChomozygous128532170
7144870450144870451C15GENIChomozygous128532171
7144870459144870460T10GENIChomozygous128532172
7144870474144870475T10GENIChomozygous128532173
7144870484144870485GA11GENIChomozygous118332851
7144870485144870486AG11GENIChomozygous118332853
7144870495144870495G9GENIChomozygous128532174
7144870523144870524T12GENIChomozygous128532175
7144870541144870542GT13GENIChomozygous115945974
7144870546144870546T14GENIChomozygous128532176
7144870550144870550G14GENIChomozygous128532177
7144870569144870569G18GENIChomozygous128532178
7144870578144870579G19GENIChomozygous128532179
7144870591144870591A19GENIChomozygous128532180
7144870279144870280CT20GENIChomozygous118261255