chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 59587110 59587111 C T 24 GENIC homozygous 51465833 10 59587678 59587679 C T 32 GENIC homozygous 51465834 10 59589767 59589768 T C 14 GENIC homozygous 51465835 10 59591293 59591300 GGCATTT ------- 20 GENIC homozygous 51465836 10 59593907 59593908 T C 25 GENIC homozygous 51465837 10 59597105 59597106 G GC 15 GENIC homozygous 51465838 10 59599284 59599285 G T 17 GENIC homozygous 51465839 10 59600128 59600129 G - 23 GENIC homozygous 51465841 10 59600682 59600683 G GTT 9 GENIC homozygous 51465843 10 59604635 59604636 T - 4 GENIC homozygous 51465844 10 59604858 59604859 A AGTGT 12 GENIC possibly homozygous 51465845 10 59604859 59604869 GTGTGTGTGT ---------- 12 GENIC heterozygous 51897795 10 59606505 59606506 C T 18 GENIC homozygous 51465846 10 59607721 59607726 TTTTT ----- 6 GENIC heterozygous 51465847 10 59607722 59607726 TTTT ---- 6 GENIC heterozygous 51465848