chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 117937084 117937085 G C 24 GENIC homozygous 596981683 8 117937113 117937114 G A 32 GENIC possibly homozygous 596981684 8 117937599 117937600 T C 20 GENIC homozygous 596981685 8 117938840 117938841 C A 2 GENIC homozygous 598380807 8 117938845 117938846 G - 4 GENIC heterozygous 727259204 8 117938987 117938989 TC -- 20 GENIC homozygous 727259205 8 117948034 117948035 T C 14 GENIC homozygous 596981686 8 117948142 117948143 T C 32 GENIC possibly homozygous 596981687 8 117954073 117954074 C T 33 GENIC possibly homozygous 596981688 8 117956795 117956796 C G 7 GENIC homozygous 598380808 8 117960587 117960588 G A 20 GENIC homozygous 596981689 8 117960691 117960694 GGG --- 6 GENIC homozygous 727259207 8 117962115 117962116 A G 20 GENIC homozygous 596981690 8 117963371 117963372 A G 4 GENIC heterozygous 596981691 8 117963462 117963463 T - 6 GENIC heterozygous 727259208 8 117963771 117963772 A G 18 GENIC homozygous 596981692 8 117968702 117968703 T G 3 GENIC heterozygous 596981693 8 117969150 117969151 T C 7 GENIC homozygous 596981694 8 117969446 117969447 A G 1 GENIC homozygous 596981695 8 117969914 117969915 T TG 19 GENIC homozygous 727259209 8 117972274 117972275 T - 8 GENIC possibly homozygous 727259210