chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	58107660	58107661	T	C	37	GENIC	homozygous	119162738
5	58107669	58107670	A	T	37	GENIC	homozygous	113816878
5	58107682	58107683	A	G	35	GENIC	homozygous	113816880
5	58107863	58107864	T	C	39	GENIC	homozygous	113816882
5	58108132	58108133	A	C	27	GENIC	homozygous	113816884
5	58108692	58108693	G	A	27	GENIC	homozygous	113816890
5	58109198	58109199	A	G	42	GENIC	homozygous	113816892
5	58109440	58109441	A	C	53	GENIC	homozygous	113816894
5	58110504	58110505	T	C	24	GENIC	homozygous	113816896
5	58112122	58112123	C	T	48	GENIC	homozygous	113816902
5	58112332	58112333	C	T	39	GENIC	homozygous	119162740
5	58112432	58112433	G	A	46	GENIC	homozygous	113816904
5	58112600	58112601	G	T	51	GENIC	homozygous	113816906
5	58112728	58112729	C	T	62	GENIC	homozygous	113816908
5	58113418	58113419	C	T	32	GENIC	homozygous	113816910
5	58114126	58114127	G	A	4	GENIC	homozygous	119201776
5	58114283	58114284	A	T	23	GENIC	homozygous	119162742
5	58114475	58114476	T	C	60	GENIC	homozygous	113816912