chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	107371510	107371511	C	T	23	GENIC	homozygous	72445054
3	107371713	107371714	C	T	22	GENIC	possibly homozygous	72074328
3	107372857	107372858	T	C	22	GENIC	homozygous	72074338
3	107374964	107374965	T	C	14	GENIC	homozygous	72074344
3	107381199	107381200	C	T	9	GENIC	homozygous	72074352
3	107382270	107382271	T	C	19	GENIC	homozygous	72074362
3	107382345	107382346	G	T	10	GENIC	possibly homozygous	72074364
3	107382432	107382433	T	G	10	GENIC	homozygous	72074368
3	107382489	107382490	G	T	19	GENIC	homozygous	72074370
3	107382532	107382533	T	C	17	GENIC	homozygous	72074374
3	107384188	107384189	T	C	27	INTERGENIC	possibly homozygous	72074386
3	107387321	107387322	G	A	5	INTERGENIC	heterozygous	72445058
3	107391156	107391157	G	A	7	INTERGENIC	possibly homozygous	72445064
3	107391709	107391710	C	T	6	INTERGENIC	heterozygous	72074404
3	107391741	107391742	G	C	5	INTERGENIC	heterozygous	72074410
3	107381259	107381260	T	G	8	GENIC	homozygous	73162557
3	107382340	107382341	T	G	11	GENIC	heterozygous	73162558
3	107391683	107391684	G	T	8	INTERGENIC	heterozygous	73162559
3	107393138	107393139	A	T	8	INTERGENIC	heterozygous	73162560
3	107398010	107398011	C	A	21	INTERGENIC	homozygous	72445067
3	107402129	107402130	A	G	17	GENIC	homozygous	72074442
3	107405853	107405854	A	C	32	GENIC	homozygous	72445082
3	107411181	107411182	G	A	4	GENIC	homozygous	72074462
3	107412950	107412951	T	A	4	GENIC	homozygous	72445086
3	107415216	107415217	C	G	24	GENIC	homozygous	72445089
3	107415483	107415484	A	G	18	GENIC	homozygous	72074478
3	107416304	107416305	A	T	6	GENIC	heterozygous	72445092
3	107416315	107416316	A	G	5	GENIC	homozygous	72445095
3	107416347	107416348	A	G	6	GENIC	heterozygous	73162561
3	107416349	107416350	G	A	7	GENIC	heterozygous	73162562
3	107416920	107416921	G	A	6	GENIC	heterozygous	72445103