chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	59562312	59562313	C	G	50	GENIC	homozygous	116831628
8	59567851	59567852	C	T	26	GENIC	possibly homozygous	116831630
8	59567855	59567856	C	T	29	GENIC	possibly homozygous	116831632
8	59568099	59568100	A	T	56	GENIC	homozygous	116512514
8	59568238	59568239	A	C	46	GENIC	homozygous	116512516
8	59574861	59574862	A	C	49	GENIC	homozygous	116512576
8	59579241	59579242	G	A	71	GENIC	heterozygous	116831634
8	59583064	59583065	T	C	40	GENIC	possibly homozygous	116512618
8	59583616	59583617	A	G	55	GENIC	homozygous	116512624
8	59585402	59585403	T	A	63	GENIC	homozygous	116831636
8	59585937	59585938	A	G	81	GENIC	homozygous	116512632
8	59586725	59586726	G	A	53	GENIC	possibly homozygous	116512634
8	59587344	59587345	C	T	71	GENIC	possibly homozygous	116512636
8	59587789	59587790	T	C	84	GENIC	homozygous	116512638
8	59588356	59588357	T	A	47	GENIC	homozygous	116512640
8	59589119	59589120	A	G	52	GENIC	homozygous	116512642
8	59589448	59589449	C	A	50	GENIC	possibly homozygous	116512644
8	59589635	59589636	G	A	82	GENIC	possibly homozygous	116512648
8	59589733	59589734	C	T	76	GENIC	homozygous	116512650
8	59589796	59589797	A	G	58	GENIC	possibly homozygous	116512652