chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8128825356128825357CG28GENIChomozygous794772123
8128827048128827049GA27GENIChomozygous794772124
8128827058128827059GA27GENIChomozygous794772125
8128827674128827675TC29GENIChomozygous794772126
8128829761128829762TC27GENIChomozygous794772127
8128830447128830448GA34GENIChomozygous794772128
8128830679128830680CT28GENIChomozygous794772129
8128831626128831627AG44GENIChomozygous794772130
8128831632128831633AG45GENIChomozygous794772131
8128832597128832598CT41GENIChomozygous794772132
8128832775128832776AG40GENIChomozygous794772133
8128832782128832783TA36GENIChomozygous794772134
8128832975128832976TC22GENIChomozygous794772135
8128833003128833004GT24GENIChomozygous794772136
8128833044128833045CT22GENICpossibly homozygous794772137
8128833256128833257CT18GENIChomozygous794772138
8128834788128834789GA32GENIChomozygous794772139
8128835989128835990AC49GENIChomozygous794772140
8128836596128836597GA36GENIChomozygous794772141
8128837857128837858CT38GENIChomozygous794772142
8128837942128837943AT50GENIChomozygous794772143
8128838964128838965AG33GENIChomozygous794772144
8128840584128840585TC32GENIChomozygous794772145
8128843659128843660GC40GENIChomozygous794772146
8128843756128843757CT35GENIChomozygous794772147
8128844347128844348TC36GENIChomozygous794772148
8128844442128844443TC39GENIChomozygous794772149
8128844691128844692TC34GENIChomozygous794772150
8128844730128844731CT35GENIChomozygous794772151
8128845096128845097AG37GENICpossibly homozygous794772152
8128845608128845609CA30GENIChomozygous794772153
8128845646128845647GT37GENIChomozygous794772154
8128846426128846427AG44GENIChomozygous794772155
8128847112128847113AG33GENIChomozygous794772156
8128848586128848587TG29GENIChomozygous794772157
8128848794128848795GA27GENIChomozygous794772158
8128848961128848962CT40GENICheterozygous794772159
8128850814128850815TC24GENIChomozygous794772160
8128851836128851837GA18GENICpossibly homozygous794772161
8128854482128854483GA34GENIChomozygous794772162