chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 51281022 51281023 C T 4 GENIC homozygous 976869641 13 51281641 51281642 C T 29 GENIC homozygous 976869642 13 51284549 51284550 A G 28 GENIC homozygous 976869643 13 51284626 51284627 A G 26 GENIC homozygous 976869644 13 51285025 51285026 G A 16 GENIC homozygous 976869645 13 51286651 51286652 C T 19 GENIC homozygous 976869646 13 51289681 51289682 T C 20 GENIC homozygous 976869647 13 51289682 51289683 T C 20 GENIC homozygous 976869648 13 51289814 51289815 G A 18 GENIC homozygous 976869649 13 51289892 51289893 T G 25 GENIC homozygous 976869650 13 51290558 51290559 T C 28 GENIC homozygous 976869651 13 51294186 51294187 C T 14 GENIC homozygous 976869652 13 51295938 51295939 G A 16 GENIC homozygous 976869653 13 51297912 51297913 C T 21 INTERGENIC heterozygous 976869654 13 51298693 51298694 G C 20 INTERGENIC homozygous 976869655 13 51298694 51298695 G A 20 INTERGENIC homozygous 976869656 13 51300057 51300058 C T 23 INTERGENIC homozygous 976869657 13 51300596 51300597 G A 26 INTERGENIC homozygous 976869658 13 51303692 51303693 T C 18 INTERGENIC homozygous 976869659 13 51304115 51304116 G A 12 INTERGENIC homozygous 976869660