chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 51281022 51281023 C T 20 GENIC possibly homozygous 809057131 13 51281641 51281642 C T 48 GENIC homozygous 809057132 13 51284549 51284550 A G 56 GENIC homozygous 809057133 13 51284626 51284627 A G 50 GENIC homozygous 809057134 13 51285025 51285026 G A 60 GENIC homozygous 809057135 13 51286651 51286652 C T 45 GENIC homozygous 809057136 13 51289681 51289682 T C 35 GENIC homozygous 809057137 13 51289682 51289683 T C 35 GENIC homozygous 809057138 13 51289814 51289815 G A 46 GENIC homozygous 809057139 13 51289892 51289893 T G 57 GENIC homozygous 809057140 13 51290558 51290559 T C 56 GENIC homozygous 809057141 13 51294186 51294187 C T 36 GENIC homozygous 809057142 13 51295938 51295939 G A 38 GENIC homozygous 809057143 13 51298693 51298694 G C 55 GENIC homozygous 809057144 13 51298694 51298695 G A 56 GENIC possibly homozygous 809057145 13 51300057 51300058 C T 49 GENIC homozygous 809057146 13 51300596 51300597 G A 54 GENIC homozygous 809057147 13 51300963 51300964 A T 8 GENIC homozygous 809057148 13 51303692 51303693 T C 38 GENIC homozygous 809057149 13 51304115 51304116 G A 45 GENIC homozygous 809057150