chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 59587110 59587111 C T 6 GENIC homozygous 51465833 10 59587678 59587679 C T 10 GENIC homozygous 51465834 10 59591663 59591664 C CTGTGTGTGTG 4 GENIC heterozygous 52460892 10 59593907 59593908 T C 13 GENIC homozygous 51465837 10 59594684 59594688 ACAC ---- 2 GENIC homozygous 52460894 10 59597105 59597106 G GC 4 GENIC homozygous 51465838 10 59599284 59599285 G T 13 GENIC homozygous 51465839 10 59600128 59600129 G - 20 GENIC homozygous 51465841 10 59600682 59600683 G GTTT 10 GENIC heterozygous 51465842 10 59600682 59600683 G GTT 10 GENIC heterozygous 51465843 10 59602077 59602079 CA -- 4 GENIC heterozygous 52460895 10 59604635 59604636 T - 4 GENIC heterozygous 51465844 10 59604858 59604859 A AGTGT 3 GENIC homozygous 51465845 10 59606505 59606506 C T 8 GENIC homozygous 51465846 10 59607722 59607726 TTTT ---- 7 GENIC heterozygous 51465848 10 59607723 59607726 TTT --- 7 GENIC heterozygous 52460897