chr start stop reference nuc variant nuc depth genic status zygosity variant ID 16 20370726 20370727 C T 39 GENIC homozygous 800602648 16 20371702 20371703 G T 34 GENIC homozygous 800602649 16 20372779 20372780 G T 42 GENIC heterozygous 800602650 16 20372782 20372783 C T 40 GENIC heterozygous 800602651 16 20373814 20373815 C T 24 GENIC homozygous 800602652 16 20374276 20374277 A G 26 GENIC possibly homozygous 800602653 16 20375359 20375360 C T 35 GENIC homozygous 800602654 16 20375440 20375441 T G 32 GENIC homozygous 800602655 16 20375700 20375701 C A 30 GENIC homozygous 800602656 16 20375702 20375703 G T 30 GENIC homozygous 800602657 16 20375827 20375828 A G 40 GENIC homozygous 800602658 16 20376160 20376161 T C 26 GENIC homozygous 800602659 16 20376386 20376387 A G 35 GENIC possibly homozygous 800602660 16 20377069 20377070 G A 39 GENIC homozygous 800602661 16 20377227 20377228 T C 33 GENIC homozygous 800602662 16 20378173 20378174 G A 33 GENIC homozygous 800602663 16 20379511 20379512 C T 39 GENIC homozygous 800602664