chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	104352881	104352882	G	A	17	GENIC	homozygous	58996163
2	104352886	104352887	A	ATGTGTG	8	GENIC	homozygous	58996164
2	104353875	104353876	C	CTG	10	GENIC	possibly homozygous	58996165
2	104358816	104358817	C	T	27	GENIC	homozygous	58996166
2	104363498	104363499	T	C	27	GENIC	homozygous	58996167
2	104364173	104364174	C	G	22	GENIC	homozygous	58996168
2	104364654	104364655	C	G	28	GENIC	homozygous	58996169
2	104365054	104365055	T	A	33	GENIC	homozygous	58996170
2	104365664	104365665	A	G	21	GENIC	homozygous	58996171
2	104366607	104366608	G	A	28	GENIC	homozygous	58996172