chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	36101740	36101741	T	A	37	GENIC	homozygous	139137401
12	36104013	36104013		ATGA	29	GENIC	homozygous	142313470
12	36105193	36105193		CTTCCTTT	15	GENIC	homozygous	142313471
12	36105209	36105210	T	C	12	GENIC	homozygous	139137403
12	36106543	36106544	A	C	41	GENIC	homozygous	139137405
12	36108889	36108890	T	C	41	GENIC	homozygous	139137408
12	36104947	36104948	T	C	6	GENIC	heterozygous	147462378
12	36104960	36104961	G	T	6	GENIC	heterozygous	147462379
12	36105841	36105842	G	A	25	GENIC	possibly homozygous	142336685
12	36108791	36108792	G	C	40	GENIC	homozygous	142336686
12	36109042	36109043	C	T	40	GENIC	homozygous	142336687
12	36106055	36106055		C	29	GENIC	homozygous	139054091