chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	61650726	61650727	A	G	17	GENIC	homozygous	111588049
3	61650927	61650928	G	A	20	GENIC	homozygous	119794553
3	61650999	61651000	A	C	26	GENIC	homozygous	119794555
3	61655625	61655626	C	T	28	GENIC	homozygous	119794557
3	61655912	61655913	T	C	17	GENIC	homozygous	111588052
3	61656205	61656206	A	G	24	GENIC	homozygous	111588053
3	61656376	61656377	C	T	19	GENIC	homozygous	111588055
3	61657453	61657453		T	18	GENIC	possibly homozygous	132953830
3	61657661	61657662	A	G	17	GENIC	homozygous	111588056
3	61658012	61658013	T	G	13	GENIC	homozygous	111588057
3	61658661	61658662	G	A	21	GENIC	homozygous	111588059
3	61660153	61660154	C	T	19	GENIC	homozygous	119794559
3	61660484	61660485	G	C	15	GENIC	homozygous	119794561
3	61661382	61661383	A	C	10	GENIC	homozygous	119794563
3	61662809	61662810	G	T	8	GENIC	homozygous	111588060
3	61655349	61655349		A	17	GENIC	homozygous	127888986
3	61662125	61662126	G	A	15	GENIC	homozygous	119854202
3	61662840	61662841	A	T	2	GENIC	homozygous	134279964
3	61662843	61662843		AGTTA	2	GENIC	homozygous	134277536
3	61666530	61666531	T	C	21	GENIC	homozygous	119854203
3	61668596	61668597	A	G	13	GENIC	homozygous	119854204