chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	59538655	59538656	A	G	22	GENIC	homozygous	51465711
10	59539489	59539493	GAGA	----	14	GENIC	homozygous	51663631
10	59541767	59541768	T	C	19	GENIC	homozygous	51465713
10	59542249	59542250	G	A	10	GENIC	homozygous	51897745
10	59545022	59545023	T	TGC	15	GENIC	homozygous	51663643
10	59545075	59545077	GT	--	12	GENIC	homozygous	51663645
10	59545796	59545797	C	T	10	GENIC	homozygous	51897749
10	59546613	59546614	T	C	18	GENIC	homozygous	51465720
10	59547003	59547005	CA	--	17	GENIC	homozygous	51465721
10	59547006	59547014	TCCTCACA	--------	18	GENIC	homozygous	51465722
10	59547664	59547665	G	A	22	GENIC	homozygous	51897751
10	59548415	59548416	G	A	12	GENIC	homozygous	51897753
10	59549576	59549577	T	C	14	GENIC	homozygous	51465725
10	59550476	59550485	ATTTATATG	---------	11	GENIC	homozygous	52379128
10	59550485	59550486	A	ACC	11	GENIC	homozygous	52379130
10	59553103	59553107	CACA	----	8	GENIC	homozygous	51465729
10	59558780	59558781	T	C	21	GENIC	homozygous	51897757
10	59562678	59562679	G	C	23	GENIC	homozygous	51465733
10	59562731	59562732	G	A	17	GENIC	homozygous	51465734
10	59563208	59563209	G	A	18	GENIC	homozygous	51663653