chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77545866375458664CA11GENIChomozygous53979236
77545867475458675AAT12GENIChomozygous53979238
77545868075458681GGT11GENIChomozygous53979240
77545868675458687TTG12GENICheterozygous53979242
77545868675458687TTGG12GENICpossibly homozygous54202576
77545870175458702C-14GENIChomozygous53979244
77545870675458710GCTC----16GENIChomozygous53979246
77546209975462100T-23GENICheterozygous53979262
77546549875465499TTTATAAGTAATTG26GENIChomozygous53979283
77548062075480621GGTCCA18GENIChomozygous53979315
77548760975487613AGAG----2GENIChomozygous54982684
77546233875462339CCAAAATCAAAATAAGATAGAGGCTACAGTATCAGAATTACAACAAAAAGA31GENICpossibly homozygous54982678
77546233875462339CCAAAATAAGATAGAGGCTACAATATCAGAATTACAACAAAAAGA31GENICheterozygous54982680
77546608375466085GT--7GENICheterozygous54982682
77548769775487698GGGAGA7GENIChomozygous54982686
77549008175490082GT25GENIChomozygous53979361
77549009275490094AA--25GENIChomozygous54907188
77549009475490095TTGC23GENIChomozygous54982688
77549015675490157TC16GENIChomozygous53979369
77549016675490167AC13GENIChomozygous53979371
77549018075490181AC19GENIChomozygous53979373
77549018375490184GC18GENIChomozygous53979375
77549024175490242G-17GENIChomozygous53979377
77549033075490331GC16GENIChomozygous53979381
77549033375490334TC14GENIChomozygous53979383
77550313975503140C-13GENICheterozygous54982690
77550314475503153CAAACAAAC---------14GENICheterozygous54982692
77551197275511974AC--9GENICheterozygous54982694