chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	39168157	39168158	C	T	27	GENIC	homozygous	52589862
8	39168162	39168163	C	T	26	GENIC	homozygous	52589863
8	39169036	39169037	C	T	59	GENIC	homozygous	52589864
8	39169225	39169226	G	A	57	GENIC	homozygous	52589865
8	39169594	39169595	A	G	27	GENIC	possibly homozygous	52589866
8	39169735	39169736	T	G	38	GENIC	homozygous	52589867
8	39169740	39169741	G	T	39	GENIC	homozygous	52589868
8	39170855	39170856	A	G	42	GENIC	homozygous	52589869
8	39170912	39170913	C	T	38	GENIC	homozygous	52589870
8	39172044	39172045	T	-	25	GENIC	homozygous	52589871
8	39172103	39172104	G	C	27	GENIC	possibly homozygous	52589872
8	39172440	39172441	G	GAA	23	GENIC	homozygous	52589873
8	39172902	39172903	A	-	22	GENIC	homozygous	52589874
8	39172993	39172994	T	-	37	GENIC	homozygous	52589875