chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 154514251 154514255 CGGC ---- 2 GENIC homozygous 745410798 3 154514276 154514277 T G 13 GENIC homozygous 630672622 3 154514414 154514415 A AGTCT 4 GENIC homozygous 745410800 3 154514475 154514476 T C 5 GENIC homozygous 630672623 3 154514477 154514478 T C 5 GENIC homozygous 630672624 3 154515475 154515476 G A 18 GENIC possibly homozygous 630672625 3 154515681 154515682 T A 16 GENIC heterozygous 630672626 3 154516008 154516009 G A 6 GENIC heterozygous 630672627 3 154516009 154516010 A T 5 GENIC heterozygous 630672628 3 154516260 154516261 T C 9 GENIC homozygous 630672629 3 154516884 154516885 A G 15 GENIC possibly homozygous 630672630 3 154517077 154517078 T C 16 GENIC possibly homozygous 630672631 3 154517156 154517157 A G 19 GENIC possibly homozygous 630672632 3 154517593 154517594 T C 15 GENIC heterozygous 630672633 3 154517632 154517633 G - 6 GENIC homozygous 745410801 3 154517898 154517899 T C 18 GENIC homozygous 630672634 3 154517982 154517986 GGCA ---- 10 GENIC heterozygous 745410802 3 154518068 154518069 G A 12 GENIC homozygous 630672635 3 154518158 154518159 T TA 19 GENIC homozygous 745410803 3 154518562 154518563 C T 30 GENIC homozygous 630672636 3 154518737 154518738 A G 17 GENIC possibly homozygous 630672637 3 154519100 154519101 C T 17 GENIC homozygous 630672638 3 154519184 154519185 C CA 5 GENIC homozygous 745410804 3 154519315 154519316 C T 20 GENIC possibly homozygous 630672639 3 154519985 154519986 A G 9 GENIC possibly homozygous 630672640 3 154520058 154520059 T C 20 GENIC homozygous 630672641 3 154520781 154520782 T C 18 GENIC homozygous 630672642 3 154520987 154520988 C T 17 GENIC possibly homozygous 630672643 3 154521914 154521915 T TAA 2 GENIC heterozygous 745410807 3 154522134 154522135 A G 23 GENIC possibly homozygous 630672644