chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 85325491 85325492 T C 6 GENIC homozygous 546077030 13 85325492 85325493 A C 4 GENIC homozygous 546077031 13 85327735 85327736 C T 18 GENIC possibly homozygous 547880907 13 85329317 85329333 CGCGCGCGCGCGCGCG ---------------- 4 GENIC homozygous 698486097 13 85329578 85329579 A ACC 13 GENIC homozygous 698486099 13 85329855 85329856 T C 17 GENIC homozygous 546077032 13 85330003 85330004 T C 23 GENIC homozygous 547880908 13 85330099 85330100 C T 19 GENIC homozygous 547880909 13 85330476 85330477 C T 14 GENIC homozygous 547880910 13 85330481 85330482 T A 12 GENIC homozygous 547880911 13 85330837 85330838 G A 23 GENIC possibly homozygous 546077033 13 85331148 85331149 T C 14 GENIC homozygous 546077034 13 85331827 85331828 T C 10 GENIC homozygous 546077035 13 85332124 85332125 A G 9 GENIC homozygous 546077036 13 85332202 85332203 C T 21 GENIC homozygous 546077037 13 85332287 85332288 T - 6 GENIC homozygous 698486102 13 85332298 85332299 G A 5 GENIC homozygous 546077038 13 85332358 85332359 A G 15 GENIC possibly homozygous 546077039 13 85332366 85332367 A G 14 GENIC possibly homozygous 546077040 13 85332413 85332414 T - 5 GENIC homozygous 698486103 13 85332415 85332417 CT -- 7 GENIC homozygous 698486104 13 85332489 85332490 C - 12 GENIC homozygous 698486105 13 85332490 85332491 G A 10 GENIC homozygous 547880912 13 85332503 85332504 G C 14 GENIC homozygous 546077041 13 85332613 85332614 C T 11 GENIC homozygous 546077042 13 85332781 85332782 A G 12 GENIC heterozygous 546077043 13 85332960 85332961 C T 14 GENIC homozygous 546077044 13 85333283 85333284 C T 20 GENIC possibly homozygous 546077045