chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 117937084 117937085 G C 18 GENIC homozygous 547456828 8 117937113 117937114 G A 18 GENIC possibly homozygous 547456829 8 117937599 117937600 T C 12 GENIC homozygous 547456830 8 117938840 117938841 C A 8 GENIC homozygous 548666412 8 117938845 117938846 G - 9 GENIC possibly homozygous 699119015 8 117938987 117938989 TC -- 16 GENIC homozygous 699119016 8 117948034 117948035 T C 20 GENIC homozygous 547456831 8 117948142 117948143 T C 27 GENIC homozygous 547456832 8 117948689 117948690 A - 2 GENIC homozygous 699119018 8 117954073 117954074 C T 27 GENIC possibly homozygous 547456833 8 117956787 117956788 T TTAGC 1 GENIC homozygous 699119019 8 117956795 117956796 C G 6 GENIC homozygous 548666413 8 117960587 117960588 G A 24 GENIC possibly homozygous 547456834 8 117960691 117960694 GGG --- 7 GENIC possibly homozygous 699119020 8 117962115 117962116 A G 21 GENIC possibly homozygous 547456835 8 117963462 117963463 T - 6 GENIC heterozygous 699119021 8 117963771 117963772 A G 23 GENIC homozygous 547456836 8 117968702 117968703 T G 6 GENIC heterozygous 547456837 8 117969150 117969151 T C 12 GENIC heterozygous 547456838 8 117969446 117969447 A G 7 GENIC homozygous 547456839 8 117969914 117969915 T TG 13 GENIC homozygous 699119022 8 117972274 117972275 T - 9 GENIC homozygous 699119023