chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101449378414493785TG33GENIChomozygous116737066
101449486714494868GA27GENIChomozygous116737067
101449576414495765AG29GENIChomozygous116859712
101449580614495807CT30GENIChomozygous116859714
101449750214497503GA30GENIChomozygous116859716
101449850414498505AC30GENIChomozygous116737068
101450084614500847TC31GENIChomozygous116737069
101450170814501709AG26GENIChomozygous116737070
101450194114501942TC26GENIChomozygous116737071
101450339314503394GC23GENIChomozygous116737072
101450481614504817CA40GENIChomozygous116737073
101450573214505733TG28GENIChomozygous116737074
101450911414509115AG33GENIChomozygous116737075
101451030714510308TA22GENIChomozygous116737076
101451589514515896GT24GENIChomozygous116737077
101451604314516044TA39GENIChomozygous116737078
101451749614517497AG34GENIChomozygous116737079