chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	135013041	135013042	G	A	49	GENIC	homozygous	114017525
5	135014215	135014216	G	T	39	GENIC	homozygous	114017528
5	135014335	135014336	A	G	41	GENIC	homozygous	114017529
5	135014399	135014400	A	G	42	GENIC	homozygous	114017530
5	135014426	135014427	C	T	37	GENIC	homozygous	114017531
5	135014777	135014778	A	G	31	GENIC	homozygous	114017532
5	135014985	135014986	G	C	29	GENIC	homozygous	114017533
5	135015282	135015283	G	A	50	GENIC	homozygous	114017534
5	135015696	135015697	T	C	37	GENIC	homozygous	114017535
5	135016052	135016053	G	A	59	GENIC	homozygous	114017536
5	135016310	135016311	T	C	38	GENIC	homozygous	114017537
5	135017089	135017090	A	G	31	GENIC	homozygous	114017538