chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
183059463830594639CT24GENICheterozygous927831918
183059464630594647AC25GENICheterozygous927831919
183059474330594744AG33GENICheterozygous927831920
183059474530594746CA34GENICheterozygous927831921
183059597530595976CT28GENICheterozygous927831922
183060006230600063TC60GENICheterozygous927831923
183060010430600105CT52GENICheterozygous927831924
183060793930607940TC49GENICheterozygous927831925
183060865630608657GA22GENICheterozygous927831926
183060871330608714GC22GENICheterozygous927831927
183060876130608762GC18GENICheterozygous927831928
183060877230608773CT18GENICheterozygous927831929
183060916530609166TA37GENICheterozygous927831930
183060916630609167AT37GENICheterozygous927831931
183060922530609226TC42GENICheterozygous927831932
183060944830609449TC36GENICheterozygous927831933
183060993730609938CG35GENICheterozygous927831934
183061192830611929CT16GENICheterozygous927831935
183061794130617943TG--102GENICheterozygous927932425
183061809330618094CG122GENICheterozygous927831936
183061812130618122AG100GENICheterozygous927831937
183063968330639684AAT15GENICheterozygous927932426
183064295730642958AG15GENICheterozygous927831938