chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 51284626 51284627 A G 26 GENIC homozygous 890476969 13 51285025 51285026 G A 21 GENIC homozygous 890476970 13 51286613 51286614 T G 8 GENIC homozygous 890476971 13 51286651 51286652 C T 19 GENIC homozygous 890476972 13 51287278 51287279 G A 7 GENIC homozygous 890476973 13 51288438 51288439 T C 15 GENIC homozygous 890476974 13 51289565 51289566 A G 21 GENIC homozygous 890476975 13 51289681 51289682 T C 4 GENIC homozygous 890476976 13 51289682 51289683 T C 4 GENIC homozygous 890476977 13 51290558 51290559 T C 17 GENIC homozygous 890476978 13 51295938 51295939 G A 9 GENIC homozygous 890476979 13 51296320 51296321 C T 5 GENIC homozygous 890476980 13 51296984 51296985 G A 16 GENIC homozygous 890476981 13 51298693 51298694 G C 4 GENIC homozygous 890476982 13 51298694 51298695 G A 4 GENIC homozygous 890476983 13 51302947 51302948 C T 7 GENIC homozygous 890476984 13 51303117 51303118 G T 11 GENIC homozygous 890476985 13 51303692 51303693 T C 6 GENIC homozygous 890476986 13 51303720 51303721 A G 12 GENIC homozygous 890476987 13 51304115 51304116 G A 4 GENIC homozygous 890476988 13 51306541 51306542 C T 16 GENIC homozygous 890476989 13 51307627 51307628 G A 18 GENIC homozygous 890476990 13 51308127 51308128 A C 9 GENIC homozygous 890476991 13 51311395 51311396 A G 17 GENIC homozygous 890476992 13 51311698 51311699 C T 12 GENIC homozygous 890476993 13 51313172 51313173 C A 20 GENIC homozygous 890476994 13 51313660 51313661 A G 15 GENIC heterozygous 890476995