chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 117937084 117937085 G C 11 GENIC homozygous 823042687 8 117937113 117937114 G A 11 GENIC homozygous 823042688 8 117937599 117937600 T C 10 GENIC homozygous 823042689 8 117938840 117938841 C A 13 GENIC homozygous 823042690 8 117938845 117938846 G - 13 GENIC homozygous 823042691 8 117938987 117938989 TC -- 14 GENIC homozygous 823042692 8 117945917 117945919 GC -- 11 GENIC homozygous 823042693 8 117948034 117948035 T C 13 GENIC homozygous 823042694 8 117948142 117948143 T C 14 GENIC homozygous 823042695 8 117954073 117954074 C T 10 GENIC homozygous 823042696 8 117956787 117956788 T TTAGC 8 GENIC homozygous 823042697 8 117956795 117956796 C G 13 GENIC homozygous 823042698 8 117960587 117960588 G A 16 GENIC homozygous 823042699 8 117960691 117960694 GGG --- 15 GENIC homozygous 823042700 8 117962115 117962116 A G 16 GENIC homozygous 823042701 8 117963462 117963463 T - 11 GENIC homozygous 823042702 8 117963771 117963772 A G 15 GENIC homozygous 823042703 8 117968702 117968703 T G 12 GENIC homozygous 823042704 8 117969150 117969151 T C 13 GENIC homozygous 823042705 8 117969446 117969447 A G 11 GENIC homozygous 823042706 8 117969914 117969915 T TG 11 GENIC homozygous 823042707 8 117972274 117972275 T - 10 GENIC homozygous 823042708