chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 132158005 132158006 C G 18 GENIC homozygous 113384154 4 132158493 132158494 G A 22 GENIC homozygous 113162891 4 132159582 132159583 A C 30 GENIC homozygous 113384156 4 132159732 132159733 T C 15 GENIC homozygous 113162896 4 132160416 132160417 C T 24 GENIC homozygous 113469856 4 132160637 132160638 C T 19 GENIC homozygous 113469858 4 132161022 132161023 T G 23 GENIC homozygous 113162898 4 132158655 132158656 C G 29 GENIC homozygous 112830875 4 132159159 132159160 T C 36 GENIC homozygous 112830876 4 132161949 132161950 A G 28 GENIC homozygous 113162904 4 132162873 132162874 G T 15 GENIC homozygous 113162908 4 132167191 132167192 C T 20 GENIC homozygous 113469860 4 132163371 132163372 C T 3 GENIC homozygous 113162910 4 132164433 132164434 A G 17 GENIC homozygous 113162914 4 132165671 132165672 A G 19 GENIC homozygous 113162918 4 132167277 132167278 C T 24 GENIC homozygous 113469862 4 132167954 132167955 G A 20 GENIC homozygous 113469864 4 132169389 132169390 T C 25 GENIC possibly homozygous 113162926 4 132169829 132169830 T C 7 GENIC homozygous 113162928 4 132171082 132171083 T C 29 GENIC homozygous 113162932