chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 49667106 49667107 T C 21 GENIC homozygous 140471088 19 49667837 49667838 T C 21 GENIC homozygous 140471089 19 49668437 49668438 A G 22 GENIC homozygous 140471090 19 49668597 49668598 G T 9 GENIC homozygous 140471091 19 49668652 49668653 A C 5 GENIC homozygous 140471092 19 49668954 49668955 G T 24 GENIC homozygous 140471093 19 49668997 49668998 A G 15 GENIC homozygous 140471094 19 49669022 49669023 A C 16 GENIC homozygous 140471095 19 49669103 49669104 A G 20 GENIC homozygous 140471096 19 49669404 49669405 C T 21 GENIC homozygous 140471097 19 49669854 49669855 G 15 GENIC homozygous 140393311 19 49671003 49671004 A G 26 GENIC homozygous 140471098 19 49671287 49671288 C T 23 GENIC homozygous 140471099 19 49671727 49671728 G T 9 GENIC homozygous 140471100 19 49672031 49672032 C A 20 GENIC homozygous 140471101 19 49673333 49673333 TCAC 23 GENIC homozygous 140393312