chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 26343068 26343069 G C 9 GENIC heterozygous 403355578 14 26343068 26343069 G 9 GENIC heterozygous 403355579 14 26392884 26392884 A 11 GENIC heterozygous 143597268 14 26632724 26632724 T 22 GENIC homozygous 139387482 14 26755551 26755552 T A 7 GENIC homozygous 154835893 14 26602131 26602132 A T 14 GENIC homozygous 139488163 14 26651713 26651714 T G 17 GENIC possibly homozygous 139488242 14 26763304 26763305 G 12 GENIC heterozygous 403355702 14 26763304 26763305 G T 12 GENIC homozygous 403355703 14 26802712 26802713 A 17 GENIC heterozygous 403355726 14 26802712 26802713 A C 17 GENIC heterozygous 403355727 14 26889449 26889450 C A 20 GENIC homozygous 139488842 14 26893756 26893758 TG 2 GENIC homozygous 141043243 14 26893757 26893758 G C 5 GENIC heterozygous 403355741 14 26893757 26893758 G 5 GENIC heterozygous 403355742 14 26893759 26893760 G C 5 GENIC heterozygous 144961556 14 26895547 26895549 AC 8 GENIC homozygous 141043244 14 26962688 26962689 G C 14 GENIC heterozygous 141120827 14 27089145 27089145 TC 12 GENIC homozygous 141043246 14 27089153 27089154 G 14 GENIC heterozygous 403355769 14 27089153 27089154 G T 14 GENIC homozygous 403355770 14 27089159 27089160 A 12 GENIC heterozygous 403355771 14 27089159 27089160 A T 12 GENIC homozygous 403355772 14 27089165 27089166 G 10 GENIC heterozygous 403355773 14 27089165 27089166 G T 10 GENIC homozygous 403355774 14 27089171 27089172 A T 11 GENIC homozygous 403355775 14 27089171 27089172 A 11 GENIC heterozygous 403355776 14 27089178 27089182 ATGA 12 GENIC homozygous 139387658 14 27089178 27089179 A 12 GENIC homozygous 403355777 14 27089178 27089179 A G 12 GENIC heterozygous 403355778 14 27089181 27089182 A 12 GENIC homozygous 403355779 14 27089181 27089182 A T 12 GENIC heterozygous 403355780 14 26755551 26755552 T 7 GENIC heterozygous 403776686 14 26962686 26962687 G C 15 GENIC heterozygous 141045230 14 27089148 27089149 G C 12 GENIC homozygous 141045231