chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	58906036	58906037	G	C	61	GENIC	homozygous	141026739
8	58906614	58906615	A	G	57	GENIC	possibly homozygous	141026740
8	58908495	58908495		A	60	GENIC	homozygous	146844069
8	58908550	58908551	G	T	57	GENIC	homozygous	146869248
8	58908995	58908996	A	G	52	GENIC	homozygous	141026744
8	58909029	58909030	T	C	54	GENIC	homozygous	141026745
8	58909391	58909392	C	T	51	GENIC	homozygous	146869250
8	58910015	58910016	G	C	50	GENIC	homozygous	141026749
8	58910901	58910901		AGTCGGATCAGAG	56	GENIC	homozygous	141015625
8	58911012	58911013	G	A	60	GENIC	homozygous	141026750
8	58911282	58911288	TGCTCT		52	GENIC	homozygous	141015626
8	58911776	58911777	C	G	37	GENIC	homozygous	141026751
8	58912692	58912693	C	A	57	GENIC	homozygous	146869251
8	58912701	58912702	A	G	56	GENIC	homozygous	141026753
8	58912988	58912990	GG		52	GENIC	homozygous	141015627
8	58913263	58913266	ACT		44	GENIC	homozygous	141015628
8	58913268	58913271	AAG		46	GENIC	homozygous	141015629
8	58913902	58913903	C	T	18	GENIC	homozygous	146869252
8	58914176	58914177	A	G	47	GENIC	homozygous	141026755