chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	69208038	69208039	G	A	42	GENIC	homozygous	112694045
4	69208317	69208318	T	G	43	GENIC	homozygous	112694049
4	69208325	69208326	C	T	44	GENIC	homozygous	112694051
4	69208335	69208336	T		43	GENIC	homozygous	133128213
4	69208339	69208340	T		45	GENIC	homozygous	133128214
4	69208343	69208344	T	C	46	GENIC	homozygous	133135856
4	69208850	69208851	G	A	14	GENIC	homozygous	112694058
4	69210103	69210104	A	T	39	GENIC	homozygous	112694064
4	69210207	69210208	G	A	40	GENIC	homozygous	112694066
4	69211181	69211182	C	T	37	GENIC	homozygous	112694070
4	69211587	69211587		CATGTCTGATA	42	GENIC	homozygous	130931730
4	69208371	69208372	T	C	45	GENIC	homozygous	113348039
4	69209794	69209795	G	A	32	GENIC	homozygous	113348041
4	69209812	69209813	G	C	34	GENIC	homozygous	113348043
4	69210889	69210890	T	C	36	GENIC	homozygous	113348045
4	69211001	69211002	G	A	31	GENIC	homozygous	113348047