chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 111676152 111676153 T C 32 GENIC homozygous 785983807 8 111676535 111676536 T C 24 GENIC homozygous 785983808 8 111676727 111676728 A C 25 GENIC homozygous 785983809 8 111677564 111677565 T C 31 GENIC homozygous 785983810 8 111677792 111677793 A G 28 GENIC homozygous 785983811 8 111678092 111678093 C T 22 GENIC homozygous 785983812 8 111678149 111678150 A G 30 GENIC homozygous 785983813 8 111678156 111678157 G C 28 GENIC homozygous 785983814 8 111679047 111679048 C G 32 GENIC homozygous 785983815 8 111680019 111680020 T C 29 GENIC homozygous 785983816 8 111680058 111680059 T C 31 GENIC homozygous 785983817 8 111682019 111682020 A G 30 GENIC homozygous 785983818 8 111682267 111682268 G A 21 GENIC homozygous 785983819 8 111682438 111682439 A G 23 GENIC homozygous 785983820 8 111683450 111683451 T C 23 GENIC homozygous 785983821 8 111684688 111684689 A G 29 GENIC homozygous 785983822 8 111684944 111684945 G A 20 GENIC homozygous 785983823 8 111685486 111685487 C T 27 GENIC homozygous 785983824 8 111685985 111685986 A G 21 GENIC homozygous 785983825