chr start stop reference nuc variant nuc depth genic status zygosity variant ID 16 20370726 20370727 C T 32 GENIC homozygous 791477002 16 20371702 20371703 G T 39 GENIC homozygous 791477003 16 20373814 20373815 C T 18 GENIC homozygous 791477004 16 20374276 20374277 A G 9 GENIC homozygous 791477005 16 20375359 20375360 C T 40 GENIC homozygous 791477006 16 20375440 20375441 T G 46 GENIC homozygous 791477007 16 20375700 20375701 C A 42 GENIC homozygous 791477008 16 20375702 20375703 G T 42 GENIC homozygous 791477009 16 20375827 20375828 A G 29 GENIC homozygous 791477010 16 20376160 20376161 T C 34 GENIC homozygous 791477011 16 20376386 20376387 A G 40 GENIC homozygous 791477012 16 20377069 20377070 G A 26 GENIC homozygous 791477013 16 20377227 20377228 T C 33 GENIC homozygous 791477014 16 20378173 20378174 G A 19 GENIC homozygous 791477015 16 20379511 20379512 C T 38 GENIC homozygous 791477016