chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107353786173537861A36GENIChomozygous128830433
107355150873551508CAA31GENIChomozygous128830436
107355599873555999CT25GENIChomozygous118001183
107355838873558389AC20GENICpossibly homozygous116800104
107355839573558396AC24GENICpossibly homozygous116800106
107357461473574615CA23GENICheterozygous116800108
107360940373609404GT6GENICheterozygous126423066
107362782573627826AG58GENIChomozygous116635347
107363088773630888AG24GENIChomozygous117064129
107363088973630890AG24GENIChomozygous117064131
107363089673630897CG17GENIChomozygous116635351
107363103673631037GC39GENIChomozygous117016600
107363103873631039AC40GENIChomozygous116978925
107363103973631040AC40GENIChomozygous117016601
107363104073631041AC40GENIChomozygous117016602
107363104273631043AG41GENIChomozygous117064133
107363108873631089C39GENIChomozygous128830475
107363109873631099TG35GENIChomozygous117016606
107363108373631084CG40GENIChomozygous117016603
107363109173631092CA38GENIChomozygous117016604
107363109473631095TG35GENIChomozygous117016605
107363110073631101GC35GENIChomozygous117016607
107363110973631110TC32GENIChomozygous117296436
107363111173631112AC32GENIChomozygous117296438
107363111473631115GC30GENIChomozygous117296440