chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	258074844	258074845	A	G	20	GENIC	homozygous	108624111
1	258092086	258092087	A	T	16	GENIC	homozygous	108781678
1	258095975	258095976	C	A	13	GENIC	homozygous	108624123
1	258098549	258098550	A	C	9	GENIC	homozygous	108624124
1	258100669	258100670	A	C	10	GENIC	homozygous	108781683
1	258100945	258100946	T	G	13	GENIC	homozygous	108624126
1	258104416	258104417	A	G	20	GENIC	homozygous	108624128
1	258106595	258106596	C	A	16	GENIC	possibly homozygous	108624130
1	258107256	258107257	T	G	13	GENIC	homozygous	108781695
1	258107259	258107260	T	C	12	GENIC	homozygous	108781696
1	258108568	258108569	C	T	18	GENIC	homozygous	108624131
1	258112382	258112383	T	A	11	GENIC	homozygous	108781701
1	258112689	258112690	A	T	2	GENIC	homozygous	120818950
1	258112690	258112691	A	T	2	GENIC	homozygous	120818951
1	258112691	258112692	C	T	2	GENIC	homozygous	120818952
1	258126263	258126264	T	C	8	GENIC	homozygous	108781706
1	258126464	258126465	T	G	13	GENIC	possibly homozygous	108781707
1	258126746	258126747	A	C	19	GENIC	homozygous	108624144
1	258126934	258126935	A	G	16	GENIC	homozygous	108781708
1	258134164	258134165	C	T	18	GENIC	homozygous	108781713
1	258137976	258137977	C	T	13	GENIC	homozygous	108781714