chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 81569476 81569477 C T 23 GENIC homozygous 979758792 9 81569886 81569887 G A 42 GENIC homozygous 979758793 9 81570188 81570189 A G 27 GENIC homozygous 979758794 9 81570600 81570601 T G 56 GENIC homozygous 979758795 9 81571248 81571249 C T 55 GENIC homozygous 979758796 9 81573648 81573649 T G 16 GENIC homozygous 979758797 9 81576118 81576119 T C 41 GENIC homozygous 979758798 9 81577184 81577185 A G 41 GENIC homozygous 979758799 9 81577573 81577574 A G 48 GENIC homozygous 979758800 9 81578643 81578644 A G 64 GENIC homozygous 979758801 9 81578769 81578770 C T 48 GENIC homozygous 979758802 9 81579388 81579389 G A 39 GENIC homozygous 979758803 9 81579430 81579431 C G 44 GENIC homozygous 979758804 9 81579641 81579642 G A 41 GENIC homozygous 979758805 9 81580350 81580351 C T 38 GENIC homozygous 979758806 9 81580734 81580735 G A 36 GENIC homozygous 979758807 9 81582241 81582242 T G 31 GENIC homozygous 979758808 9 81582445 81582446 A G 35 GENIC homozygous 979758809 9 81583368 81583369 G A 28 GENIC homozygous 979758810 9 81583743 81583744 T C 49 GENIC homozygous 979758811 9 81583954 81583955 T A 37 GENIC homozygous 979758812 9 81584203 81584204 C T 48 GENIC homozygous 979758813 9 81584220 81584221 T C 58 GENIC homozygous 979758814 9 81586177 81586178 T A 67 GENIC homozygous 979758815