chr start stop reference nuc variant nuc depth genic status zygosity variant ID 16 3350775 3350775 C 58 GENIC homozygous 131171256 16 3350778 3350779 A T 58 GENIC homozygous 111922555 16 3350807 3350808 A G 65 GENIC homozygous 111922557 16 3350832 3350833 C A 62 GENIC possibly homozygous 111922559 16 3351222 3351223 G A 52 GENIC homozygous 111922561 16 3353255 3353256 C T 76 GENIC homozygous 111700521 16 3353528 3353529 C T 53 GENIC homozygous 111922564 16 3353529 3353530 A G 53 GENIC homozygous 111700525 16 3354410 3354411 C T 50 GENIC homozygous 111922566 16 3354893 3354894 T C 51 GENIC homozygous 111700533 16 3354912 3354913 T C 54 GENIC homozygous 111700535 16 3351261 3351261 T 60 GENIC homozygous 129327633 16 3352493 3352494 A C 55 GENIC homozygous 112345996