chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	136148354	136148355	A	G	64	GENIC	homozygous	137630814
5	136149155	136149156	G	C	69	GENIC	homozygous	137630815
5	136150378	136150382	CCCA		46	GENIC	homozygous	137344051
5	136150576	136150577	A	C	58	GENIC	homozygous	137630816
5	136151257	136151258	C	T	73	GENIC	homozygous	137630817
5	136152232	136152233	A	G	60	GENIC	homozygous	137630818
5	136152914	136152915	A	T	48	GENIC	homozygous	137630819
5	136153151	136153152	C	T	48	GENIC	homozygous	137630820
5	136154094	136154095	G	A	51	GENIC	homozygous	137630821
5	136154561	136154562	T	G	48	GENIC	homozygous	137630822
5	136155504	136155504		A	57	GENIC	possibly homozygous	137344052
5	136156331	136156332	A	G	61	GENIC	homozygous	137630823
5	136156407	136156408	T	C	58	GENIC	homozygous	137630824
5	136160333	136160334	C	T	43	GENIC	homozygous	137630825
5	136160420	136160421	T	C	46	GENIC	homozygous	137630826
5	136160514	136160515	T	G	53	GENIC	homozygous	137630827
5	136160930	136160931	C	T	40	GENIC	homozygous	137630828
5	136161535	136161536	C	G	48	GENIC	homozygous	137630829
5	136164915	136164916	G	A	53	GENIC	homozygous	137630830
5	136165066	136165067	G	A	40	GENIC	homozygous	137630831
5	136166214	136166215	T	G	53	GENIC	homozygous	137630832
5	136166239	136166240	A	G	49	GENIC	homozygous	137630833
5	136166418	136166419	T	C	55	GENIC	homozygous	137630834
5	136166940	136166941	A	G	49	GENIC	homozygous	137630835
5	136167466	136167467	G	A	44	GENIC	homozygous	137630836
5	136158249	136158250	T	C	41	GENIC	possibly homozygous	154326991
5	136158249	136158250	T		41	GENIC	heterozygous	403159418