chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 101157985 101157986 T C 12 GENIC homozygous 116709060 10 101159108 101159109 T C 18 GENIC homozygous 116957739 10 101159354 101159355 A C 24 GENIC homozygous 116957741 10 101159772 101159773 G A 23 GENIC homozygous 116709066 10 101160074 101160075 G A 15 GENIC homozygous 116957743 10 101160461 101160462 A G 15 GENIC homozygous 116957745 10 101160640 101160641 A G 23 GENIC homozygous 116957747 10 101160687 101160688 T C 13 GENIC homozygous 116957749 10 101160757 101160758 C T 9 GENIC homozygous 116957751 10 101160794 101160795 G A 10 GENIC homozygous 116957753 10 101160899 101160900 C T 24 GENIC homozygous 116957755 10 101160988 101160989 G A 25 GENIC homozygous 116957757 10 101161121 101161122 C T 16 GENIC homozygous 116957759 10 101161140 101161141 G C 12 GENIC homozygous 116957761 10 101161758 101161759 C T 21 GENIC homozygous 116957763 10 101161868 101161869 G T 24 GENIC homozygous 116957765 10 101162040 101162041 A C 18 GENIC homozygous 116957767 10 101162379 101162380 A G 25 GENIC homozygous 116957769 10 101163537 101163538 T G 16 GENIC homozygous 116957771 10 101167532 101167533 A G 8 GENIC homozygous 116957773 10 101167819 101167820 T C 7 GENIC homozygous 116709068 10 101169181 101169182 C T 25 GENIC homozygous 116957775 10 101171630 101171631 A G 11 GENIC homozygous 116957777 10 101172354 101172355 G A 20 GENIC homozygous 116957779 10 101172898 101172899 A G 19 GENIC homozygous 116957781 10 101173299 101173300 C A 15 GENIC homozygous 116957783 10 101173326 101173327 C T 17 GENIC homozygous 116957785 10 101173754 101173755 T G 15 GENIC homozygous 116709070 10 101170877 101170878 A C 7 GENIC homozygous 117313378 10 101170871 101170872 A C 7 GENIC homozygous 117313376