chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4109467323109467324GT30GENIChomozygous113597883
4109467516109467517AG29GENIChomozygous113372800
4109467772109467773GC33GENIChomozygous113372804
4109467780109467781AG34GENIChomozygous113372806
4109468185109468186CT12GENIChomozygous113372808
4109468355109468356CG27GENIChomozygous113372810
4109468458109468459AT36GENIChomozygous113372812
4109468865109468866AG29GENIChomozygous113372813
4109468888109468889TG28GENIChomozygous113372815
4109469117109469118AT21GENIChomozygous113597885
4109469568109469569CT23GENIChomozygous113372819
4109469602109469603GA19GENIChomozygous113597887
4109469674109469675CT15GENIChomozygous113372821
4109470228109470229AG35GENIChomozygous113597889
4109470467109470468CA27GENIChomozygous113597891
4109470508109470509GT24GENIChomozygous113372823