chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77545866375458664CA10GENIChomozygous53979236
77545867475458675AAT11GENIChomozygous53979238
77545868075458681GGT14GENIChomozygous53979240
77545868675458687TTGG11GENIChomozygous54202576
77545870175458702C-13GENIChomozygous53979244
77545870675458710GCTC----15GENIChomozygous53979246
77546209975462100T-33GENICheterozygous53979262
77546233775462338AAGAAAAT18GENICheterozygous55027243
77546549875465499TTTATAAGTAATTG23GENIChomozygous53979283
77547904875479050AG--4GENICheterozygous55027245
77548062075480621GGTCCA22GENIChomozygous53979315
77548769775487698GGGAGA5GENIChomozygous54982686
77546233875462339CCAAAATCAAAATAAGATAGAGGCTACAGTATCAGAATTACAACAAAAAGA22GENICpossibly homozygous54982678
77546233875462339CCAAAATAAGATAGAGGCTACAATATCAGAATTACAACAAAAAGA22GENICheterozygous54982680
77546608375466085GT--8GENICheterozygous54982682
77548760975487613AGAG----2GENIChomozygous54982684
77549008175490082GT25GENIChomozygous53979361
77549009275490094AA--24GENIChomozygous54907188
77549009475490095TTGC23GENIChomozygous54982688
77549015675490157TC36GENIChomozygous53979369
77549016675490167AC40GENIChomozygous53979371
77549018075490181AC37GENIChomozygous53979373
77549018375490184GC37GENIChomozygous53979375
77549024175490242G-26GENIChomozygous53979377
77549033075490331GC33GENIChomozygous53979381
77549033375490334TC35GENIChomozygous53979383
77550139375501397GACA----21GENICheterozygous54658660
77550990775509909TG--25GENICheterozygous55027247
77551027075510271CCTCTCT13GENIChomozygous53979530
77551190175511903AC--4GENICheterozygous54202583