chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 154514251 154514255 CGGC ---- 13 GENIC homozygous 711922879 3 154514276 154514277 T G 17 GENIC homozygous 569347743 3 154514414 154514415 A AGTCT 13 GENIC homozygous 711922881 3 154514475 154514476 T C 18 GENIC homozygous 569347744 3 154514477 154514478 T C 19 GENIC homozygous 569347745 3 154515475 154515476 G A 22 GENIC homozygous 569347746 3 154515681 154515682 T A 8 GENIC homozygous 569347747 3 154516008 154516009 G A 19 GENIC homozygous 569347748 3 154516009 154516010 A T 19 GENIC homozygous 569347749 3 154516260 154516261 T C 13 GENIC homozygous 569347750 3 154516884 154516885 A G 28 GENIC homozygous 569347751 3 154517077 154517078 T C 27 GENIC homozygous 571347786 3 154517156 154517157 A G 23 GENIC homozygous 569347752 3 154517593 154517594 T C 23 GENIC homozygous 569347753 3 154517632 154517633 G - 18 GENIC homozygous 711922882 3 154517898 154517899 T C 11 GENIC homozygous 569347754 3 154517982 154517986 GGCA ---- 18 GENIC homozygous 711922883 3 154518068 154518069 G A 17 GENIC homozygous 569347755 3 154518158 154518159 T TA 22 GENIC homozygous 711922884 3 154518562 154518563 C T 14 GENIC homozygous 571347787 3 154518737 154518738 A G 19 GENIC homozygous 569347756 3 154518931 154518932 G GT 11 GENIC heterozygous 711922885 3 154519100 154519101 C T 7 GENIC homozygous 571347788 3 154519184 154519185 C CA 4 GENIC homozygous 711922886 3 154519315 154519316 C T 12 GENIC homozygous 569347757 3 154519896 154519897 C CTT 17 GENIC possibly homozygous 711922889 3 154519985 154519986 A G 19 GENIC homozygous 569347758 3 154520058 154520059 T C 18 GENIC homozygous 569347759 3 154520781 154520782 T C 22 GENIC homozygous 569347760 3 154520987 154520988 C T 16 GENIC homozygous 569347761 3 154521914 154521915 T TAA 12 GENIC possibly homozygous 711922891 3 154521930 154521931 A AC 10 GENIC heterozygous 711922892 3 154522134 154522135 A G 18 GENIC homozygous 569347762