chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	59538655	59538656	A	G	14	GENIC	possibly homozygous	51465711
10	59541297	59541298	A	C	25	GENIC	possibly homozygous	51465712
10	59541767	59541768	T	C	30	GENIC	possibly homozygous	51465713
10	59542904	59542905	C	T	5	GENIC	homozygous	51465714
10	59546613	59546614	T	C	16	GENIC	homozygous	51465720
10	59547006	59547014	TCCTCACA	--------	2	GENIC	homozygous	51465722
10	59548863	59548864	A	AAG	8	GENIC	homozygous	51465724
10	59549576	59549577	T	C	20	GENIC	homozygous	51465725
10	59550593	59550594	A	G	11	GENIC	heterozygous	51465726
10	59551182	59551184	GA	--	5	GENIC	heterozygous	51465727
10	59562678	59562679	G	C	26	GENIC	homozygous	51465733
10	59562731	59562732	G	A	23	GENIC	homozygous	51465734