chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	51120982	51120983	C	T	44	GENIC	homozygous	111565761
3	51121104	51121105	C	T	50	GENIC	homozygous	111565762
3	51121345	51121346	A	G	27	GENIC	homozygous	111565763
3	51122595	51122596	T	A	34	GENIC	homozygous	111565764
3	51122608	51122609	A	G	29	GENIC	homozygous	111565765
3	51122703	51122704	G	T	20	GENIC	homozygous	111565766
3	51122924	51122925	A	G	32	GENIC	homozygous	111565767
3	51123665	51123666	C	T	38	GENIC	homozygous	111565768
3	51125037	51125038	A	G	28	GENIC	homozygous	111565770
3	51125637	51125638	A	G	37	GENIC	homozygous	111565771
3	51125965	51125966	C	T	43	GENIC	homozygous	111565772
3	51126349	51126350	A	G	40	GENIC	homozygous	111565773
3	51127101	51127102	T	C	36	GENIC	homozygous	111565774
3	51127784	51127785	A	G	29	GENIC	homozygous	111565775
3	51128622	51128623	G	A	28	GENIC	homozygous	111565776