chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	36101740	36101741	T	A	51	GENIC	homozygous	139137401
12	36104013	36104013		ATGA	33	GENIC	homozygous	142313470
12	36105193	36105193		CTTCCTTT	7	GENIC	homozygous	142313471
12	36106055	36106055		C	29	GENIC	homozygous	139054091
12	36105209	36105210	T	C	7	GENIC	homozygous	139137403
12	36106543	36106544	A	C	51	GENIC	homozygous	139137405
12	36108889	36108890	T	C	49	GENIC	homozygous	139137408
12	36105841	36105842	G	A	43	GENIC	homozygous	142336685
12	36108791	36108792	G	C	38	GENIC	homozygous	142336686
12	36109042	36109043	C	T	51	GENIC	homozygous	142336687