chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	107372857	107372858	T	C	55	GENIC	homozygous	72074338
3	107374964	107374965	T	C	61	GENIC	homozygous	72074344
3	107381199	107381200	C	T	38	GENIC	homozygous	72074352
3	107381348	107381349	T	G	14	GENIC	homozygous	72074354
3	107382270	107382271	T	C	40	GENIC	homozygous	72074362
3	107382345	107382346	G	T	38	GENIC	possibly homozygous	72074364
3	107382432	107382433	T	G	35	GENIC	homozygous	72074368
3	107382489	107382490	G	T	43	GENIC	homozygous	72074370
3	107382532	107382533	T	C	66	GENIC	homozygous	72074374
3	107384002	107384003	G	A	102	INTERGENIC	heterozygous	72074384
3	107384188	107384189	T	C	59	INTERGENIC	homozygous	72074386
3	107388930	107388931	C	T	2	INTERGENIC	homozygous	72445061
3	107393170	107393171	G	A	45	INTERGENIC	homozygous	73628485
3	107387254	107387255	G	A	75	INTERGENIC	heterozygous	74860240
3	107390957	107390958	G	A	29	INTERGENIC	possibly homozygous	74860243
3	107401793	107401794	G	A	49	INTERGENIC	possibly homozygous	73750964
3	107402129	107402130	A	G	55	GENIC	homozygous	72074442
3	107410764	107410765	T	A	85	GENIC	heterozygous	72074460
3	107410782	107410783	T	C	89	GENIC	heterozygous	72445084
3	107411162	107411163	G	A	53	GENIC	homozygous	74860246
3	107411181	107411182	G	A	48	GENIC	homozygous	72074462
3	107415483	107415484	A	G	54	GENIC	homozygous	72074478
3	107415979	107415980	T	C	73	GENIC	heterozygous	72074480
3	107416120	107416121	C	A	46	GENIC	possibly homozygous	72074484