chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
51403436014034361AT14GENIChomozygous55210644
51403511614035117AC44GENIChomozygous55210645
51403678314036784A-13GENICheterozygous55210646
51403845614038457AT26GENIChomozygous55210647
51404146014041461GC20GENIChomozygous55210650
51404319714043198AAT25GENICpossibly homozygous55210651
51403743414037435AT25GENIChomozygous57215712
51403937614039378AT--24GENIChomozygous57215714
51404010614040107CCT3GENICheterozygous56395265
51404382514043826TTACAC8GENICheterozygous55210653
51404384214043844AC--8GENICpossibly homozygous57215716
51404423214044233A-25GENICpossibly homozygous55210654
51404482714044829TT--4GENIChomozygous55210655
51404488614044887GGT6GENIChomozygous56610243
51404508714045088T-12GENIChomozygous55210658
51404509114045092TA11GENIChomozygous56337276
51404673114046733TG--26GENIChomozygous57215718
51404830814048309TC32GENIChomozygous57215720
51404923514049236CCTTTTTTTTT9GENIChomozygous56395278
51405129814051299T-30GENIChomozygous55210659
51405257014052571TC29GENIChomozygous57215722
51405386614053867GA31GENIChomozygous55210660
51405603014056032GG--1GENIChomozygous55210661
51405603114056032GGTTTTTT1GENIChomozygous56395281
51405608714056088GT1GENIChomozygous55210662
51405609014056091TC1GENIChomozygous55210663
51405644814056449GGTTTTT4GENICheterozygous56577576
51405658914056590CCT13GENIChomozygous55210665
51405644814056449GGTTT4GENICheterozygous55863358
51404405814044059CCT16GENICpossibly homozygous56869532