chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	81565384	81565385	T	C	44	GENIC	possibly homozygous	109878134
2	81565435	81565436	A	C	57	GENIC	homozygous	109878136
2	81565452	81565453	A	T	52	GENIC	homozygous	109878138
2	81565455	81565456	G	A	54	GENIC	homozygous	109878140
2	81565527	81565528	G	T	50	GENIC	possibly homozygous	109878142
2	81565557	81565558	T	A	48	GENIC	homozygous	109878144
2	81565852	81565853	A	T	57	GENIC	homozygous	109878146
2	81565925	81565926	C	T	58	GENIC	possibly homozygous	109878148
2	81566050	81566051	A	G	33	GENIC	possibly homozygous	109878150
2	81566051	81566052	C	T	32	GENIC	possibly homozygous	109878152
2	81566060	81566061	G	T	33	GENIC	homozygous	109878154
2	81566211	81566212	T	C	19	GENIC	homozygous	109878156
2	81566212	81566213	G	A	19	GENIC	homozygous	109878158
2	81566234	81566235	G	C	22	GENIC	homozygous	109878160
2	81566277	81566278	G	A	26	GENIC	homozygous	109878162
2	81566294	81566295	A	T	23	GENIC	homozygous	109878164
2	81566322	81566323	C	T	27	GENIC	homozygous	109878166
2	81566377	81566378	C	A	33	GENIC	homozygous	109878168
2	81566457	81566458	A	G	18	GENIC	possibly homozygous	109878170
2	81566650	81566651	T	C	34	GENIC	homozygous	109878172
2	81566655	81566656	C	T	34	GENIC	homozygous	109878174
2	81566660	81566661	T	C	35	GENIC	homozygous	109878176
2	81566783	81566784	T	C	43	GENIC	homozygous	109878178
2	81566912	81566913	G	A	43	GENIC	possibly homozygous	109878179
2	81567103	81567104	G	C	32	GENIC	homozygous	109878181
2	81567334	81567335	A	G	33	GENIC	homozygous	109878183