chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 7093197 7093198 G A 11 GENIC homozygous 931624755 3 7093844 7093845 C T 3 GENIC heterozygous 931624756 3 7097542 7097543 G T 15 GENIC homozygous 931624757 3 7098295 7098296 C T 7 GENIC homozygous 931624758 3 7098369 7098370 C T 14 GENIC homozygous 931624759 3 7099818 7099819 G A 11 GENIC homozygous 931624760 3 7100982 7100983 A G 9 GENIC homozygous 931624761 3 7102967 7102968 G A 5 GENIC homozygous 931624762 3 7104113 7104114 G A 8 GENIC homozygous 931624763 3 7104503 7104504 T C 4 GENIC homozygous 931624764 3 7104695 7104696 C G 8 GENIC homozygous 931624765 3 7105391 7105392 C T 12 GENIC homozygous 931624766 3 7105471 7105472 G T 9 GENIC homozygous 931624767 3 7106196 7106197 A G 7 GENIC homozygous 931624768 3 7107692 7107693 G C 11 GENIC homozygous 931624769 3 7107968 7107969 C T 8 GENIC homozygous 931624770 3 7108132 7108133 T C 7 GENIC homozygous 931624771 3 7108363 7108364 T C 9 GENIC homozygous 931624772 3 7109040 7109041 C T 9 GENIC homozygous 931624773 3 7109054 7109055 T C 7 GENIC homozygous 931624774 3 7109638 7109639 A G 11 GENIC homozygous 931624775 3 7111026 7111027 G A 4 GENIC homozygous 931624776 3 7113120 7113121 C T 7 GENIC homozygous 931624777 3 7114183 7114184 G A 9 GENIC homozygous 931624778 3 7114384 7114385 C T 11 GENIC homozygous 931624779 3 7116979 7116980 A G 5 GENIC homozygous 931624780 3 7117209 7117210 G A 10 GENIC homozygous 931624781 3 7118811 7118812 C G 7 GENIC homozygous 931624782 3 7119476 7119477 G A 9 GENIC homozygous 931624783 3 7121880 7121881 G A 8 GENIC homozygous 931624784 3 7123987 7123988 G A 14 GENIC homozygous 931624785 3 7127362 7127363 A G 7 GENIC homozygous 931624786 3 7128528 7128529 A T 7 GENIC homozygous 931624787