chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 94355635 94355636 A G 40 GENIC homozygous 116826350 10 94358852 94358852 A 55 GENIC homozygous 128847405 10 94360477 94360478 C T 45 GENIC homozygous 116685060 10 94357906 94357907 G A 65 GENIC homozygous 116954859 10 94357996 94357997 C T 65 GENIC homozygous 116954861 10 94360597 94360598 C A 50 GENIC homozygous 116954863 10 94361306 94361307 C A 53 GENIC homozygous 116826352 10 94362086 94362087 C T 39 GENIC homozygous 116826356 10 94362196 94362197 A T 43 GENIC homozygous 116685064 10 94362617 94362618 T G 45 GENIC homozygous 116685068 10 94362686 94362687 T C 41 GENIC homozygous 116826360 10 94363354 94363355 C A 39 GENIC homozygous 116826362 10 94363481 94363482 A G 30 GENIC homozygous 116685072 10 94365561 94365562 A C 40 GENIC possibly homozygous 116826366 10 94365715 94365716 T C 36 GENIC possibly homozygous 116826368 10 94365944 94365945 G A 38 GENIC homozygous 116954865 10 94366516 94366517 T A 18 GENIC homozygous 118126091 10 94367244 94367245 C A 46 GENIC homozygous 116954867 10 94368125 94368126 G A 41 GENIC homozygous 116685082 10 94368384 94368385 G C 54 GENIC homozygous 116685084 10 94376942 94376943 T 36 GENIC homozygous 128847408