chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 32505974 32505975 T TGC 12 GENIC heterozygous 830252926 20 32507543 32507544 C CA 18 GENIC heterozygous 830252927 20 32508682 32508683 C - 20 GENIC homozygous 830252928 20 32508749 32508750 C - 15 GENIC homozygous 830252929 20 32531774 32531775 A - 11 GENIC homozygous 830252930 20 32531836 32531837 C A 12 GENIC homozygous 830252931 20 32531839 32531840 C T 11 GENIC homozygous 830252932 20 32531854 32531855 A G 11 GENIC homozygous 830252933 20 32531859 32531860 C - 11 GENIC homozygous 830252934 20 32531862 32531863 C T 11 GENIC homozygous 830252935 20 32531870 32531871 C CA 3 GENIC homozygous 830252936 20 32531871 32531872 C A 3 GENIC homozygous 830252937 20 32531874 32531875 C A 5 GENIC homozygous 830252938 20 32531883 32531884 C G 5 GENIC homozygous 830252939 20 32531893 32531894 C A 5 GENIC homozygous 830252940 20 32531897 32531898 C A 5 GENIC homozygous 830252941 20 32531900 32531901 C CT 5 GENIC homozygous 830252942 20 32531954 32531955 C A 15 GENIC homozygous 830252943 20 32531958 32531959 G - 12 GENIC homozygous 830252944 20 32531960 32531961 G A 12 GENIC homozygous 830252945