chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	120580863	120580864	G	T	49	GENIC	homozygous	116081784
7	120581591	120581592	G	C	35	GENIC	homozygous	116081785
7	120582131	120582132	C	T	43	GENIC	homozygous	116081786
7	120582647	120582648	C	T	25	GENIC	possibly homozygous	116081788
7	120582545	120582546	C		27	GENIC	homozygous	132657303
7	120584610	120584611	G	A	43	GENIC	homozygous	116081790
7	120585126	120585127	C	T	41	GENIC	homozygous	115856776
7	120587006	120587007	A	G	38	GENIC	homozygous	116081791
7	120587462	120587463	A	G	36	GENIC	homozygous	115856778
7	120587816	120587817	C	T	37	GENIC	homozygous	116081792
7	120588701	120588702	C	T	55	GENIC	homozygous	116081793
7	120589153	120589154	C		33	GENIC	homozygous	132657304
7	120589906	120589907	G	A	52	GENIC	homozygous	116081794
7	120590954	120590954		G	37	GENIC	homozygous	132657305
7	120591364	120591365	G	A	60	GENIC	homozygous	116081795
7	120591759	120591760	A	G	43	GENIC	homozygous	116081796
7	120591980	120591981	C	G	42	GENIC	homozygous	116081797
7	120591982	120591983	A	T	41	GENIC	homozygous	116081798