chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101449378414493785TG28GENIChomozygous116737066
101449486714494868GA29GENIChomozygous116737067
101449576414495765AG24GENIChomozygous116859712
101449580614495807CT18GENIChomozygous116859714
101449750214497503GA18GENIChomozygous116859716
101449850414498505AC27GENIChomozygous116737068
101449964314499644AG6GENIChomozygous117249186
101449964914499650AC3GENIChomozygous117249188
101450084614500847TC39GENIChomozygous116737069
101450170814501709AG20GENIChomozygous116737070
101450194114501942TC28GENIChomozygous116737071
101450339314503394GC16GENIChomozygous116737072
101450481614504817CA8GENIChomozygous116737073
101450573214505733TG24GENIChomozygous116737074
101450911414509115AG17GENIChomozygous116737075
101451030714510308TA20GENIChomozygous116737076
101451589514515896GT18GENIChomozygous116737077
101451604314516044TA25GENIChomozygous116737078
101451749614517497AG17GENIChomozygous116737079