chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8106451570106451571TA18GENIChomozygous116628928
8106453272106453273TC23GENIChomozygous116628930
8106453565106453566CT22GENIChomozygous116628932
8106454816106454817TG34GENICheterozygous116628934
8106454969106454970CA29GENIChomozygous116628936
8106456895106456896AG27GENIChomozygous116628938
8106458388106458389CG24GENIChomozygous116628942
8106460360106460361TG12GENIChomozygous116628944
8106461462106461463GA29GENIChomozygous116628946
8106462917106462918TC23GENIChomozygous116628948
8106463968106463969GA28GENIChomozygous116628950
8106464866106464867AG24GENIChomozygous116628952
8106465096106465097CT11GENIChomozygous116628954
8106466972106466973AG19GENIChomozygous116628956
8106468644106468645TC19GENIChomozygous116628958