chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 154514251 154514255 CGGC ---- 13 GENIC homozygous 709837246 3 154514276 154514277 T G 14 GENIC homozygous 565975695 3 154514414 154514415 A AGTCT 13 GENIC homozygous 709837248 3 154514475 154514476 T C 11 GENIC homozygous 565975696 3 154514477 154514478 T C 11 GENIC homozygous 565975697 3 154515475 154515476 G A 12 GENIC homozygous 565975698 3 154515681 154515682 T A 12 GENIC homozygous 565975699 3 154516008 154516009 G A 18 GENIC homozygous 565975700 3 154516009 154516010 A T 18 GENIC homozygous 565975701 3 154516260 154516261 T C 22 GENIC homozygous 565975702 3 154516884 154516885 A G 25 GENIC homozygous 565975703 3 154517077 154517078 T C 22 GENIC homozygous 568006920 3 154517156 154517157 A G 31 GENIC homozygous 565975704 3 154517593 154517594 T C 13 GENIC homozygous 565975705 3 154517632 154517633 G - 21 GENIC homozygous 709837249 3 154517898 154517899 T C 22 GENIC homozygous 565975706 3 154517982 154517986 GGCA ---- 16 GENIC homozygous 709837250 3 154518068 154518069 G A 16 GENIC possibly homozygous 565975707 3 154518158 154518159 T TA 28 GENIC homozygous 709837251 3 154518562 154518563 C T 19 GENIC homozygous 568006921 3 154518737 154518738 A G 17 GENIC homozygous 565975708 3 154518931 154518932 G GT 20 GENIC possibly homozygous 709837252 3 154519100 154519101 C T 10 GENIC homozygous 568006922 3 154519184 154519185 C CA 4 GENIC homozygous 709837253 3 154519315 154519316 C T 12 GENIC homozygous 565975709 3 154519896 154519897 C CTT 17 GENIC homozygous 709837256 3 154519985 154519986 A G 28 GENIC homozygous 565975710 3 154520058 154520059 T C 26 GENIC homozygous 565975711 3 154520781 154520782 T C 15 GENIC homozygous 565975712 3 154520987 154520988 C T 17 GENIC homozygous 565975713 3 154521914 154521915 T TAA 10 GENIC homozygous 709837258 3 154521930 154521931 A AC 12 GENIC heterozygous 709837259 3 154522134 154522135 A G 16 GENIC homozygous 565975714