chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45781155157811552AG26GENIChomozygous644455590
45781202057812021AAT24GENIChomozygous753744001
45781274557812746CT25GENIChomozygous644455591
45781318357813184CA18GENIChomozygous644455592
45781799257817994AA--17GENICheterozygous753744002
45781799357817994A-17GENICpossibly homozygous753744003
45781818657818187GA18GENIChomozygous644455593
45781827257818273CCT6GENIChomozygous753744006
45781837457818375CCT13GENICpossibly homozygous753744007
45781842657818427AG28GENIChomozygous644455594
45781858857818589GT22GENIChomozygous644455595
45781859457818595CT24GENIChomozygous644455596
45781866157818662GA29GENIChomozygous644455597
45781913757819138A-29GENICpossibly homozygous753744008
45781915057819151AG29GENICpossibly homozygous644455598
45781930557819306CA30GENIChomozygous644455599
45781978057819781GA22GENIChomozygous644455600
45781981657819817T-21GENIChomozygous753744009
45782029657820297GT25GENIChomozygous644455601
45782038757820388TC18GENIChomozygous644455602
45782148057821481GT33GENIChomozygous644455603