chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 25929592 25929593 G C 27 GENIC homozygous 953231002 13 25930014 25930015 C G 27 GENIC homozygous 953231003 13 25932098 25932099 A G 19 GENIC homozygous 953231004 13 25933968 25933969 A G 19 GENIC homozygous 953231005 13 25934709 25934710 G T 14 GENIC homozygous 953231006 13 25935708 25935709 C T 22 GENIC homozygous 953231007 13 25935922 25935923 G A 20 GENIC homozygous 953231008 13 25939690 25939691 C T 25 GENIC homozygous 953231009 13 25939981 25939982 C G 25 GENIC homozygous 953231010 13 25940180 25940181 C A 19 GENIC homozygous 953231011 13 25940369 25940370 G A 21 GENIC homozygous 953231012 13 25941095 25941096 T C 20 GENIC homozygous 953231013 13 25941195 25941196 C A 32 GENIC homozygous 953231014 13 25941208 25941209 C T 31 GENIC homozygous 953231015 13 25941736 25941737 A G 35 GENIC homozygous 953231016 13 25942084 25942085 C T 24 GENIC homozygous 953231017 13 25943081 25943082 G A 44 GENIC homozygous 953231018 13 25945548 25945549 C T 28 GENIC homozygous 953231019 13 25949824 25949825 T A 26 GENIC homozygous 953231020