chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 154514251 154514255 CGGC ---- 19 GENIC homozygous 725526779 3 154514276 154514277 T G 20 GENIC homozygous 592443183 3 154514414 154514415 A AGTCT 15 GENIC homozygous 725526781 3 154514475 154514476 T C 26 GENIC homozygous 592443184 3 154514477 154514478 T C 26 GENIC homozygous 592443185 3 154515475 154515476 G A 18 GENIC homozygous 592443186 3 154515681 154515682 T A 18 GENIC homozygous 592443187 3 154516008 154516009 G A 27 GENIC homozygous 592443188 3 154516009 154516010 A T 28 GENIC homozygous 592443189 3 154516260 154516261 T C 32 GENIC homozygous 592443190 3 154516884 154516885 A G 36 GENIC homozygous 592443191 3 154517077 154517078 T C 36 GENIC homozygous 594397566 3 154517156 154517157 A G 31 GENIC homozygous 592443192 3 154517593 154517594 T C 20 GENIC homozygous 592443193 3 154517632 154517633 G - 27 GENIC homozygous 725526782 3 154517898 154517899 T C 25 GENIC homozygous 592443194 3 154517982 154517986 GGCA ---- 23 GENIC homozygous 725526783 3 154518068 154518069 G A 30 GENIC homozygous 592443195 3 154518158 154518159 T TA 31 GENIC homozygous 725526784 3 154518562 154518563 C T 33 GENIC homozygous 594397567 3 154518737 154518738 A G 15 GENIC homozygous 592443196 3 154518931 154518932 G GT 20 GENIC possibly homozygous 725526785 3 154519100 154519101 C T 27 GENIC homozygous 594397568 3 154519176 154519177 C - 8 GENIC heterozygous 725526786 3 154519184 154519185 C CA 8 GENIC possibly homozygous 725526787 3 154519315 154519316 C T 25 GENIC homozygous 592443197 3 154519896 154519897 C CTT 19 GENIC homozygous 725526790 3 154519985 154519986 A G 40 GENIC homozygous 592443198 3 154520058 154520059 T C 33 GENIC homozygous 592443199 3 154520781 154520782 T C 17 GENIC homozygous 592443200 3 154520987 154520988 C T 23 GENIC homozygous 592443201 3 154521914 154521915 T TAA 12 GENIC homozygous 725526792 3 154521930 154521931 A AC 11 GENIC heterozygous 725526793 3 154522134 154522135 A G 32 GENIC homozygous 592443202