chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	104352169	104352170	G	A	31	GENIC	homozygous	60124969
2	104352886	104352887	A	ATGTGTGTGTGTG	4	GENIC	homozygous	60492463
2	104353046	104353047	A	G	31	GENIC	homozygous	60124970
2	104353875	104353876	C	CTCTGTGTG	12	GENIC	heterozygous	60492464
2	104353875	104353876	C	CTCTGTGTGTG	12	GENIC	heterozygous	60492465
2	104355552	104355553	C	A	28	GENIC	homozygous	60124972
2	104356056	104356057	T	C	27	GENIC	homozygous	60124973
2	104357052	104357053	C	T	24	GENIC	homozygous	60124974
2	104361015	104361016	C	T	46	GENIC	homozygous	60124975
2	104361307	104361308	C	T	29	GENIC	homozygous	60124976
2	104361925	104361926	T	C	41	GENIC	homozygous	60124977
2	104362668	104362669	T	G	44	GENIC	homozygous	60124978
2	104363498	104363499	T	C	24	GENIC	homozygous	58996167
2	104363715	104363716	T	C	21	GENIC	homozygous	60124979
2	104364173	104364174	C	G	23	GENIC	homozygous	58996168
2	104364654	104364655	C	G	38	GENIC	homozygous	58996169
2	104365606	104365607	G	GTGGTGAA	29	GENIC	homozygous	60448702