chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 109234226 109234227 A G 11 GENIC homozygous 51598886 10 109234708 109234709 C T 26 GENIC possibly homozygous 51955911 10 109235466 109235467 C T 22 GENIC homozygous 51955914 10 109236132 109236133 T C 21 GENIC possibly homozygous 51598891 10 109237508 109237509 C T 5 GENIC homozygous 51955917 10 109237956 109237957 C T 17 GENIC heterozygous 51955923 10 109239663 109239664 C T 13 GENIC possibly homozygous 51955926 10 109243542 109243543 C T 14 GENIC possibly homozygous 51955929 10 109245772 109245773 G GC 7 GENIC heterozygous 51598933 10 109245783 109245784 T C 10 GENIC heterozygous 51598934 10 109247074 109247075 A G 7 GENIC heterozygous 51598937 10 109247683 109247684 A G 14 GENIC possibly homozygous 51598942 10 109248741 109248742 G A 25 GENIC homozygous 51955935 10 109249412 109249413 G C 7 GENIC heterozygous 51955938 10 109248301 109248418 CCCTCGTTTCTCTTTTTTGGTTCTTTTTTTTTTTTTTTTTTTTTTCGGAGCTGGAGACCGAACCCAGGGTCTTGCGCTTCCTATGTAAGCGCTCTACCACTGAGCTAAATCCCCAGC --------------------------------------------------------------------------------------------------------------------- 21 GENIC heterozygous 52331770