chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 25929592 25929593 G C 25 GENIC homozygous 961975866 13 25930014 25930015 C G 27 GENIC homozygous 961975867 13 25932098 25932099 A G 21 GENIC homozygous 961975868 13 25933968 25933969 A G 20 GENIC homozygous 961975869 13 25934709 25934710 G T 14 GENIC homozygous 961975870 13 25935708 25935709 C T 18 GENIC homozygous 961975871 13 25935922 25935923 G A 19 GENIC homozygous 961975872 13 25939690 25939691 C T 21 GENIC homozygous 961975873 13 25939981 25939982 C G 16 GENIC homozygous 961975874 13 25940180 25940181 C A 26 GENIC homozygous 961975875 13 25940369 25940370 G A 17 GENIC homozygous 961975876 13 25941095 25941096 T C 17 GENIC homozygous 961975877 13 25941195 25941196 C A 21 GENIC homozygous 961975878 13 25941208 25941209 C T 23 GENIC homozygous 961975879 13 25941736 25941737 A G 31 GENIC homozygous 961975880 13 25942084 25942085 C T 23 GENIC homozygous 961975881 13 25943081 25943082 G A 57 GENIC homozygous 961975882 13 25945548 25945549 C T 22 GENIC homozygous 961975883 13 25949824 25949825 T A 27 GENIC possibly homozygous 961975884