chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 51284626 51284627 A G 16 GENIC homozygous 994849080 13 51285025 51285026 G A 34 GENIC homozygous 994849081 13 51286613 51286614 T G 29 GENIC homozygous 994849082 13 51286651 51286652 C T 30 GENIC possibly homozygous 994849083 13 51287278 51287279 G A 21 GENIC possibly homozygous 994849084 13 51288438 51288439 T C 23 GENIC possibly homozygous 994849085 13 51289565 51289566 A G 27 GENIC homozygous 994849086 13 51289681 51289682 T C 28 GENIC homozygous 994849087 13 51289682 51289683 T C 27 GENIC homozygous 994849088 13 51290558 51290559 T C 28 GENIC homozygous 994849089 13 51290598 51290599 G A 27 GENIC possibly homozygous 994849090 13 51295938 51295939 G A 21 GENIC possibly homozygous 994849091 13 51296320 51296321 C T 29 GENIC possibly homozygous 994849092 13 51296984 51296985 G A 19 GENIC homozygous 994849093 13 51298693 51298694 G C 40 INTERGENIC possibly homozygous 994849094 13 51298694 51298695 G A 42 INTERGENIC possibly homozygous 994849095 13 51302947 51302948 C T 30 INTERGENIC homozygous 994849096 13 51303117 51303118 G T 33 INTERGENIC possibly homozygous 994849097 13 51303692 51303693 T C 21 INTERGENIC homozygous 994849098 13 51303720 51303721 A G 28 INTERGENIC homozygous 994849099 13 51304115 51304116 G A 23 INTERGENIC possibly homozygous 994849100 13 51306541 51306542 C T 21 INTERGENIC possibly homozygous 994849101 13 51307627 51307628 G A 14 INTERGENIC homozygous 994849102 13 51307971 51307972 A G 20 INTERGENIC possibly homozygous 994849103 13 51311395 51311396 A G 16 INTERGENIC homozygous 994849104 13 51313172 51313173 C A 24 INTERGENIC possibly homozygous 994849105