chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 51281022 51281023 C T 36 GENIC homozygous 980165120 13 51281641 51281642 C T 16 GENIC homozygous 980165121 13 51284549 51284550 A G 49 GENIC homozygous 980165122 13 51284626 51284627 A G 42 GENIC possibly homozygous 980165123 13 51285025 51285026 G A 40 GENIC homozygous 980165124 13 51286651 51286652 C T 36 GENIC homozygous 980165125 13 51289681 51289682 T C 28 GENIC homozygous 980165126 13 51289682 51289683 T C 28 GENIC homozygous 980165127 13 51289814 51289815 G A 46 GENIC homozygous 980165128 13 51289892 51289893 T G 39 GENIC homozygous 980165129 13 51290558 51290559 T C 52 GENIC homozygous 980165130 13 51294186 51294187 C T 77 GENIC homozygous 980165131 13 51295938 51295939 G A 11 GENIC homozygous 980165132 13 51298693 51298694 G C 53 INTERGENIC homozygous 980165133 13 51298694 51298695 G A 52 INTERGENIC homozygous 980165134 13 51300057 51300058 C T 28 INTERGENIC homozygous 980165135 13 51300596 51300597 G A 21 INTERGENIC homozygous 980165136 13 51303692 51303693 T C 43 INTERGENIC homozygous 980165137 13 51304115 51304116 G A 5 INTERGENIC homozygous 980165138