chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	4690311	4690311		A	32	GENIC	homozygous	138233585
8	4690529	4690536	ATAAGTA		30	GENIC	homozygous	138233586
8	4690800	4690801	C	T	52	GENIC	homozygous	138278957
8	4691386	4691387	C	T	50	GENIC	homozygous	138278958
8	4691780	4691781	G	A	43	GENIC	homozygous	138278959
8	4692484	4692485	G	T	45	GENIC	homozygous	138278960
8	4693061	4693061		G	13	GENIC	homozygous	138233587
8	4693303	4693304	C	T	34	GENIC	homozygous	138278964
8	4693779	4693780	G	A	42	GENIC	homozygous	138278965
8	4693848	4693848		T	37	GENIC	homozygous	138233588
8	4694123	4694124	G	A	42	GENIC	homozygous	138278966
8	4694220	4694220		A	44	GENIC	homozygous	138233589
8	4694968	4694969	G	A	34	GENIC	homozygous	138278967
8	4694998	4694999	T		33	GENIC	homozygous	138233590
8	4695225	4695226	T	C	37	GENIC	homozygous	138278968
8	4695807	4695808	A	G	44	GENIC	homozygous	138278969
8	4695822	4695823	G	C	46	GENIC	homozygous	138278970
8	4696724	4696725	G	A	41	GENIC	homozygous	138278971
8	4696733	4696734	T	C	42	GENIC	homozygous	138278972
8	4696919	4696920	C	T	38	GENIC	homozygous	138278973
8	4697416	4697417	C	T	46	GENIC	homozygous	138278974
8	4693059	4693060	A	G	13	GENIC	homozygous	403228939
8	4693059	4693060	A		13	GENIC	heterozygous	403228940