chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7144865735144865736AG43GENIChomozygous115945964
7144866560144866561TC55GENIChomozygous115945966
7144869078144869079AG55GENIChomozygous115945967
7144869376144869377CA81GENICheterozygous115945969
7144869686144869687GA72GENICheterozygous115945971
7144870245144870245T45GENIChomozygous128532158
7144870150144870151T38GENIChomozygous128532154
7144870187144870187G39GENIChomozygous128532155
7144870203144870203G44GENIChomozygous128532156
7144870219144870219G45GENIChomozygous128532157
7144870279144870280CT42GENIChomozygous118261255
7144870280144870281TC41GENIChomozygous116101369
7144870284144870284A41GENIChomozygous128532159
7144870311144870312A34GENIChomozygous128532160
7144870323144870323TA32GENIChomozygous128532161
7144870331144870332C27GENIChomozygous128532162
7144870334144870335G27GENIChomozygous128532163
7144870352144870353G20GENIChomozygous128532164
7144870358144870359T19GENIChomozygous128532165
7144870361144870361AG17GENIChomozygous128532166
7144870373144870374GT11GENIChomozygous115945972
7144870459144870460T17GENIChomozygous128532172
7144870474144870475T16GENIChomozygous128532173
7144870495144870495G17GENIChomozygous128532174
7144870523144870524T26GENIChomozygous128532175
7144870541144870542GT30GENIChomozygous115945974
7144870546144870546T30GENIChomozygous128532176
7144870550144870550G31GENIChomozygous128532177
7144870569144870569G29GENIChomozygous128532178
7144870578144870579G27GENIChomozygous128532179
7144870591144870591A25GENIChomozygous128532180
7144870485144870486AG18GENIChomozygous118332853
7144870316144870317AC34GENIChomozygous118339331
7144870484144870485GA18GENIChomozygous118332851