chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	109862295	109862296	T	C	7	GENIC	homozygous	119739750
3	109862297	109862298	C	A	7	GENIC	homozygous	119800217
3	109863499	109863500	T	C	18	GENIC	homozygous	111671539
3	109864005	109864006	A	C	19	GENIC	homozygous	111671541
3	109865884	109865885	A	C	10	GENIC	homozygous	111671543
3	109866356	109866357	A	G	18	GENIC	homozygous	111671544
3	109866952	109866953	A	T	19	GENIC	homozygous	111671546
3	109867388	109867389	G	C	31	GENIC	possibly homozygous	111671556
3	109867403	109867404	A	T	28	GENIC	homozygous	111671558
3	109867927	109867928	G	T	15	GENIC	homozygous	111671560
3	109868819	109868820	T	C	18	GENIC	homozygous	111671562
3	109869141	109869142	A	G	29	GENIC	homozygous	111671564
3	109869509	109869510	A	T	22	GENIC	homozygous	111671565
3	109870864	109870865	A	G	34	GENIC	homozygous	112428520
3	109871040	109871041	A	G	15	GENIC	homozygous	111671569
3	109871405	109871406	C	A	25	GENIC	homozygous	111671571
3	109871811	109871812	G	A	29	GENIC	homozygous	111671573
3	109871840	109871841	G	A	37	GENIC	homozygous	112428521