chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 143485148 143485149 C T 22 GENIC possibly homozygous 597400746 5 143485641 143485642 C CAAA 1 GENIC homozygous 727091798 5 143489159 143489160 A C 17 GENIC possibly homozygous 595537760 5 143489322 143489323 G A 32 GENIC possibly homozygous 595537761 5 143489800 143489801 C T 18 GENIC homozygous 595537762 5 143491429 143491430 A G 26 GENIC possibly homozygous 595537763 5 143492236 143492237 C T 29 GENIC possibly homozygous 595537764 5 143492336 143492337 A T 13 GENIC heterozygous 597400747 5 143492550 143492551 G A 16 GENIC homozygous 595537765 5 143494974 143494975 C T 14 GENIC homozygous 595537766 5 143495081 143495082 A AGCAT 7 GENIC homozygous 727091800 5 143496622 143496623 T C 21 GENIC homozygous 595537767 5 143500431 143500432 G T 2 GENIC heterozygous 597400748 5 143500737 143500739 TA -- 1 GENIC homozygous 727091802 5 143504816 143504817 C T 19 GENIC homozygous 597400749 5 143504944 143504945 T TAA 2 GENIC heterozygous 727091805 5 143504945 143504946 A - 2 GENIC heterozygous 727091804 5 143505501 143505502 G GAAA 2 GENIC heterozygous 727091806 5 143506093 143506094 G A 19 GENIC homozygous 597400750 5 143512103 143512104 C T 16 GENIC possibly homozygous 597400751 5 143513758 143513759 G GA 2 GENIC heterozygous 727091808 5 143519278 143519279 T A 20 GENIC homozygous 597400752 5 143519809 143519810 C G 17 GENIC possibly homozygous 597400753 5 143522265 143522266 T TG 5 GENIC heterozygous 727091810 5 143522505 143522506 T - 11 GENIC homozygous 727091811 5 143526655 143526656 A G 25 GENIC homozygous 595537768 5 143527141 143527142 A C 16 GENIC heterozygous 595537769 5 143527395 143527396 T C 14 GENIC homozygous 595537770 5 143529180 143529181 A T 15 GENIC homozygous 597400754 5 143529368 143529369 C T 32 GENIC homozygous 595537771