chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	61634427	61634428	C	T	57	GENIC	homozygous	111588036
3	61634489	61634490	G	A	50	GENIC	homozygous	111588037
3	61634527	61634528	C	T	43	GENIC	homozygous	111588038
3	61639427	61639428	C	T	46	GENIC	homozygous	111588039
3	61641797	61641798	C	T	51	GENIC	homozygous	111588041
3	61642548	61642549	C	T	51	GENIC	homozygous	111588042
3	61642853	61642854	G	A	53	GENIC	homozygous	111588043
3	61645926	61645927	T	G	58	GENIC	homozygous	111588044
3	61646262	61646263	A	T	69	GENIC	homozygous	111588045
3	61646990	61646991	T	A	41	GENIC	homozygous	111588046
3	61649897	61649898	A	G	41	GENIC	homozygous	111588047
3	61650345	61650346	T	G	59	GENIC	homozygous	111588048
3	61650726	61650727	A	G	20	GENIC	homozygous	111588049
3	61640544	61640545	A		42	GENIC	homozygous	127888980
3	61641350	61641351	G		18	GENIC	homozygous	127888981
3	61642475	61642478	TTG		30	GENIC	homozygous	127888982
3	61645237	61645240	GTC		49	GENIC	homozygous	127888983
3	61645455	61645456	A		60	GENIC	homozygous	127888984
3	61649709	61649709		C	48	GENIC	homozygous	127888985