chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 234536778 234536779 C T 17 GENIC possibly homozygous 591628097 1 234536903 234536904 A T 24 GENIC possibly homozygous 591628098 1 234537481 234537482 G A 14 GENIC homozygous 589689812 1 234537502 234537503 T C 12 GENIC homozygous 591628099 1 234538935 234538936 A G 15 GENIC homozygous 589689813 1 234540396 234540397 G A 23 GENIC homozygous 589689814 1 234540546 234540547 A T 15 GENIC possibly homozygous 591628100 1 234541348 234541349 A C 14 GENIC possibly homozygous 589689815 1 234541919 234541920 C T 17 GENIC heterozygous 589689816 1 234542072 234542073 C A 10 GENIC homozygous 591628101 1 234542195 234542196 C T 5 GENIC heterozygous 591628102 1 234542845 234542846 T C 8 GENIC homozygous 589689817 1 234543307 234543308 C - 7 GENIC homozygous 723294943 1 234546078 234546079 C CAAAAAAA 1 GENIC homozygous 723294946 1 234546752 234546753 A C 12 GENIC homozygous 591628103 1 234548180 234548181 T A 13 GENIC possibly homozygous 591628104 1 234548632 234548633 G A 12 GENIC possibly homozygous 589689818 1 234548703 234548704 A C 15 GENIC homozygous 591628105 1 234549190 234549191 T C 11 GENIC homozygous 591628106 1 234549211 234549212 C G 15 GENIC homozygous 589689819 1 234549523 234549524 G A 14 GENIC possibly homozygous 591628107 1 234549900 234549901 T C 12 GENIC homozygous 589689820 1 234550635 234550636 G A 13 GENIC homozygous 591628108