chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 111309537 111309538 A T 28 GENIC heterozygous 823449827 10 111309564 111309565 G GT 18 GENIC heterozygous 823449828 10 111309785 111309786 G A 11 GENIC heterozygous 823449829 10 111309838 111309839 T G 16 GENIC homozygous 823449830 10 111309877 111309878 G A 11 GENIC homozygous 823449831 10 111309880 111309881 C A 10 GENIC homozygous 823449832 10 111309882 111309883 T C 10 GENIC homozygous 823449833 10 111310878 111310879 C A 12 GENIC heterozygous 823449834 10 111310903 111310904 T A 11 GENIC heterozygous 823449835 10 111311394 111311395 T C 24 GENIC heterozygous 823449836 10 111319715 111319716 C CT 17 GENIC heterozygous 823449837 10 111319740 111319741 G A 18 GENIC heterozygous 823449838 10 111320871 111320872 T C 25 GENIC heterozygous 823449839 10 111320895 111320896 G A 29 GENIC heterozygous 823449840 10 111320944 111320945 T A 28 GENIC heterozygous 823449841 10 111320961 111320962 G T 22 GENIC heterozygous 823449842 10 111321173 111321174 A G 19 GENIC heterozygous 823449843 10 111321687 111321688 C G 21 GENIC heterozygous 823449844 10 111321756 111321757 T C 23 GENIC heterozygous 823449845 10 111321773 111321774 A G 25 GENIC heterozygous 823449846 10 111321805 111321806 G A 29 GENIC heterozygous 823449847 10 111321904 111321905 G C 25 GENIC heterozygous 823449848 10 111321971 111321972 G C 31 GENIC heterozygous 823449849 10 111322012 111322013 A T 23 GENIC heterozygous 823449850