chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 86029547 86029548 G A 21 GENIC homozygous 995041072 14 86029588 86029589 T C 21 GENIC homozygous 995041073 14 86030362 86030363 T G 27 GENIC possibly homozygous 995041074 14 86031325 86031326 T C 36 GENIC possibly homozygous 995041075 14 86032735 86032736 T C 33 GENIC homozygous 995041076 14 86032736 86032737 G A 32 GENIC homozygous 995041077 14 86032817 86032818 T C 26 GENIC homozygous 995041078 14 86033359 86033360 T C 17 GENIC possibly homozygous 995041079 14 86034018 86034019 C T 29 GENIC possibly homozygous 995041080 14 86034038 86034039 T C 33 GENIC possibly homozygous 995041081 14 86034609 86034610 T C 24 GENIC homozygous 995041082 14 86039956 86039957 G T 22 GENIC possibly homozygous 995041083 14 86040251 86040252 C T 25 GENIC possibly homozygous 995041084 14 86041800 86041801 A G 18 GENIC possibly homozygous 995041085 14 86041890 86041891 C T 21 GENIC possibly homozygous 995041086 14 86042554 86042555 A G 20 GENIC possibly homozygous 995041087 14 86042830 86042831 C T 26 GENIC possibly homozygous 995041088 14 86042864 86042865 A G 30 GENIC possibly homozygous 995041089 14 86043726 86043727 G T 19 GENIC homozygous 995041090 14 86043848 86043849 T C 29 GENIC possibly homozygous 995041091 14 86044089 86044090 G A 19 GENIC possibly homozygous 995041092 14 86044324 86044325 C G 24 GENIC possibly homozygous 995041093