chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	135663813	135663813		C	45	GENIC	homozygous	131650188
5	135664103	135664104	G	T	47	GENIC	possibly homozygous	118845740
5	135669568	135669569	A	G	49	GENIC	homozygous	114018310
5	135669628	135669629	T	C	49	GENIC	homozygous	114144694
5	135664105	135664106	G	T	47	GENIC	homozygous	118858469
5	135668822	135668823	G	A	49	GENIC	homozygous	114144691
5	135669118	135669119	T	C	50	GENIC	homozygous	114144692
5	135669593	135669594	G	A	43	GENIC	homozygous	114144693
5	135664804	135664805	C	T	49	GENIC	homozygous	114442540
5	135666369	135666370	C	T	49	GENIC	homozygous	114442544
5	135668452	135668453	T	C	46	GENIC	homozygous	114442546
5	135669823	135669824	T	C	50	GENIC	homozygous	114144695
5	135669857	135669858	A	C	51	GENIC	homozygous	114144696
5	135672173	135672174	T	C	53	GENIC	homozygous	114144699
5	135672497	135672498	C	T	33	GENIC	homozygous	114144700
5	135672864	135672865	T	C	53	GENIC	homozygous	114018312
5	135673053	135673054	G	A	54	GENIC	homozygous	114144702
5	135673187	135673188	A	G	46	GENIC	homozygous	114144703
5	135673910	135673911	A	G	66	GENIC	homozygous	114144704
5	135673963	135673964	C	T	57	GENIC	homozygous	114442548
5	135674186	135674187	G	A	53	GENIC	homozygous	114442550
5	135674254	135674255	A	G	60	GENIC	homozygous	114144705
5	135674298	135674299	C	T	58	GENIC	homozygous	114144706
5	135674436	135674437	T	C	41	GENIC	homozygous	114144707
5	135674786	135674787	T	C	39	GENIC	homozygous	114144708
5	135674974	135674975	T	C	55	GENIC	homozygous	114144709
5	135675084	135675085	C	T	41	GENIC	homozygous	114144710
5	135667484	135667484		CTC	41	GENIC	homozygous	128242493
5	135669740	135669740		AACT	46	GENIC	homozygous	130962658
5	135670189	135670190	A		41	GENIC	homozygous	130962660