chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 230302912 230302913 G T 16 GENIC homozygous 74936780 2 230303065 230303066 G T 25 GENIC homozygous 75571530 2 230303066 230303067 T C 24 GENIC homozygous 75571532 2 230303165 230303166 A T 23 GENIC homozygous 74936781 2 230303246 230303247 G A 16 GENIC homozygous 74936782 2 230303717 230303718 A G 15 GENIC homozygous 74936783 2 230303788 230303789 G A 15 GENIC homozygous 74936784 2 230303796 230303797 G A 15 GENIC homozygous 74936785 2 230303810 230303811 G A 17 GENIC homozygous 74936786 2 230304441 230304442 C T 12 GENIC homozygous 74936787 2 230304889 230304890 A G 18 GENIC homozygous 74936788 2 230305196 230305197 G A 15 GENIC possibly homozygous 74936789 2 230305761 230305762 G A 18 GENIC homozygous 74936790 2 230305937 230305938 A G 15 GENIC homozygous 74441416 2 230305193 230305194 T C 16 GENIC homozygous 74441414 2 230306437 230306438 G A 15 GENIC homozygous 74936791 2 230306825 230306826 C A 25 GENIC homozygous 74936792 2 230306845 230306846 G A 26 GENIC homozygous 74936793 2 230307170 230307171 A G 18 GENIC homozygous 74936794 2 230307240 230307241 C T 30 GENIC homozygous 74936795 2 230307310 230307311 T C 27 GENIC homozygous 74441418 2 230307649 230307650 G A 26 GENIC homozygous 74936796