chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10111309537111309538AT28GENICheterozygous823449827
10111309564111309565GGT18GENICheterozygous823449828
10111309785111309786GA11GENICheterozygous823449829
10111309838111309839TG16GENIChomozygous823449830
10111309877111309878GA11GENIChomozygous823449831
10111309880111309881CA10GENIChomozygous823449832
10111309882111309883TC10GENIChomozygous823449833
10111310878111310879CA12GENICheterozygous823449834
10111310903111310904TA11GENICheterozygous823449835
10111311394111311395TC24GENICheterozygous823449836
10111319715111319716CCT17GENICheterozygous823449837
10111319740111319741GA18GENICheterozygous823449838
10111320871111320872TC25GENICheterozygous823449839
10111320895111320896GA29GENICheterozygous823449840
10111320944111320945TA28GENICheterozygous823449841
10111320961111320962GT22GENICheterozygous823449842
10111321173111321174AG19GENICheterozygous823449843
10111321687111321688CG21GENICheterozygous823449844
10111321756111321757TC23GENICheterozygous823449845
10111321773111321774AG25GENICheterozygous823449846
10111321805111321806GA29GENICheterozygous823449847
10111321904111321905GC25GENICheterozygous823449848
10111321971111321972GC31GENICheterozygous823449849
10111322012111322013AT23GENICheterozygous823449850