chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 25929592 25929593 G C 31 GENIC homozygous 956020735 13 25930014 25930015 C G 31 GENIC homozygous 956020736 13 25932098 25932099 A G 28 GENIC homozygous 956020737 13 25933968 25933969 A G 27 GENIC homozygous 956020738 13 25934709 25934710 G T 20 GENIC homozygous 956020739 13 25935708 25935709 C T 29 GENIC homozygous 956020740 13 25935922 25935923 G A 22 GENIC homozygous 956020741 13 25939690 25939691 C T 18 GENIC homozygous 956020742 13 25939981 25939982 C G 10 GENIC homozygous 956020743 13 25940180 25940181 C A 14 GENIC homozygous 956020744 13 25940369 25940370 G A 16 GENIC homozygous 956020745 13 25941095 25941096 T C 22 GENIC homozygous 956020746 13 25941195 25941196 C A 21 GENIC homozygous 956020747 13 25941208 25941209 C T 19 GENIC homozygous 956020748 13 25941736 25941737 A G 38 GENIC homozygous 956020749 13 25942084 25942085 C T 22 GENIC possibly homozygous 956020750 13 25943081 25943082 G A 46 GENIC homozygous 956020751 13 25945548 25945549 C T 30 GENIC homozygous 956020752 13 25949824 25949825 T A 39 GENIC homozygous 956020753