chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
42061773420617735CT112GENICheterozygous112540717
42061773820617739TC105GENICheterozygous112540719
42061790720617908CA30GENIChomozygous112540721
42061799120617992CT55GENICheterozygous112999138
42061813920618140TG57GENICpossibly homozygous112540723
42061830420618305CA76GENICheterozygous112999139
42061844420618445TC75GENIChomozygous112540725
42061853920618540GT71GENICheterozygous112540727
42061868120618682CT77GENICheterozygous112540729
42061872920618730GA69GENICheterozygous112999140
42061899020618991CA52GENIChomozygous112540731
42061933420619335AT73GENICpossibly homozygous112540733
42061956920619570AT80GENICheterozygous112999141
42062000520620006AG91GENICheterozygous112540735
42062001420620015CT97GENICheterozygous112540737
42062003220620033CT109GENICheterozygous112999142
42062016920620170AG75GENICheterozygous112999143
42062062320620624TA185GENICheterozygous112540739
42062063520620636AT199GENICheterozygous112540741
42062115820621159CG62GENICheterozygous112999144
42062151020621511AG68GENIChomozygous112540743