chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	61634427	61634428	C	T	43	GENIC	homozygous	111588036
3	61634489	61634490	G	A	35	GENIC	homozygous	111588037
3	61634527	61634528	C	T	33	GENIC	homozygous	111588038
3	61639427	61639428	C	T	40	GENIC	homozygous	111588039
3	61640544	61640545	A		42	GENIC	homozygous	127888980
3	61641797	61641798	C	T	45	GENIC	homozygous	111588041
3	61642475	61642478	TTG		39	GENIC	homozygous	127888982
3	61642548	61642549	C	T	42	GENIC	homozygous	111588042
3	61642853	61642854	G	A	46	GENIC	homozygous	111588043
3	61645237	61645240	GTC		59	GENIC	homozygous	127888983
3	61645455	61645456	A		65	GENIC	homozygous	127888984
3	61645926	61645927	T	G	50	GENIC	homozygous	111588044
3	61646262	61646263	A	T	47	GENIC	homozygous	111588045
3	61646990	61646991	T	A	40	GENIC	homozygous	111588046
3	61649709	61649709		C	45	GENIC	homozygous	127888985
3	61649897	61649898	A	G	49	GENIC	homozygous	111588047
3	61650345	61650346	T	G	49	GENIC	homozygous	111588048
3	61650726	61650727	A	G	28	GENIC	homozygous	111588049