chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 40911047 40911048 G GA 11 GENIC possibly homozygous 50323516 12 40912021 40912022 C T 34 GENIC homozygous 50323518 12 40912070 40912071 T C 28 GENIC homozygous 50205005 12 40913010 40913011 G A 25 GENIC homozygous 50323520 12 40913630 40913631 A AAC 2 GENIC heterozygous 50543799 12 40914306 40914307 T C 23 GENIC homozygous 50205006 12 40914573 40914574 G T 18 GENIC homozygous 50205007 12 40914712 40914714 TT -- 13 GENIC heterozygous 50323524 12 40914713 40914714 T - 13 GENIC heterozygous 50205008 12 40915753 40915754 T TTCTCCCAAG 17 GENIC homozygous 50205010 12 40916039 40916040 C - 13 GENIC homozygous 50323526 12 40916041 40916057 TTTGAAAAGGCAAGCG ---------------- 14 GENIC homozygous 50323528 12 40916203 40916204 C - 2 GENIC heterozygous 50323530 12 40917344 40917345 A G 14 GENIC homozygous 50205012 12 40917592 40917593 T TG 4 GENIC homozygous 50205013 12 40917780 40917781 T C 10 GENIC homozygous 50205014