chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	206028680	206028681	T	C	53	GENIC	homozygous	74681966
1	206028824	206028825	T	G	52	GENIC	homozygous	74681968
1	206029441	206029442	G	A	56	GENIC	homozygous	74681970
1	206029752	206029753	A	G	37	GENIC	homozygous	74681972
1	206030964	206030965	A	C	47	GENIC	homozygous	74681974
1	206030965	206030966	A	C	46	GENIC	homozygous	74681976
1	206031092	206031093	A	C	59	GENIC	homozygous	74681978
1	206032348	206032349	G	A	47	GENIC	homozygous	75478258
1	206032545	206032546	A	G	39	GENIC	possibly homozygous	74681982
1	206032628	206032629	A	C	39	GENIC	heterozygous	74681984
1	206033339	206033340	C	T	56	GENIC	homozygous	74681986
1	206033503	206033504	G	A	48	GENIC	homozygous	74681988
1	206034134	206034135	C	A	41	GENIC	possibly homozygous	74681990
1	206034405	206034406	G	T	63	GENIC	heterozygous	74681992
1	206035075	206035076	C	T	46	GENIC	homozygous	74681994
1	206035548	206035549	A	G	38	GENIC	homozygous	74681996
1	206035682	206035683	A	G	51	GENIC	homozygous	74681998
1	206036331	206036332	A	G	51	GENIC	homozygous	74682000
1	206036667	206036668	T	C	12	GENIC	homozygous	74682002
1	206037110	206037111	T	A	55	GENIC	homozygous	74682004
1	206037169	206037170	C	G	56	GENIC	homozygous	74682006
1	206037642	206037643	G	A	41	GENIC	possibly homozygous	74682008
1	206037746	206037747	G	A	60	GENIC	possibly homozygous	74682010
1	206038074	206038075	A	G	47	GENIC	homozygous	74682012
1	206038214	206038215	T	C	57	GENIC	homozygous	74682014
1	206038270	206038271	G	A	52	GENIC	homozygous	74682016
1	206038322	206038323	A	T	56	GENIC	homozygous	74682018
1	206038951	206038952	T	A	56	GENIC	heterozygous	74682020
1	206038963	206038964	A	G	44	GENIC	homozygous	74682022
1	206039298	206039299	T	C	67	GENIC	homozygous	74682024