chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	109862475	109862476	C	T	20	GENIC	homozygous	111671524
3	109862502	109862503	C	T	22	GENIC	homozygous	111671526
3	109862519	109862520	A	C	22	GENIC	homozygous	111671528
3	109862528	109862529	G	T	20	GENIC	homozygous	111671530
3	109862578	109862579	G	T	18	GENIC	homozygous	111671532
3	109862587	109862588	G	A	17	GENIC	homozygous	119894575
3	109862874	109862875	T	C	31	GENIC	homozygous	111671534
3	109863499	109863500	T	C	28	GENIC	homozygous	111671539
3	109864005	109864006	A	C	16	GENIC	homozygous	111671541
3	109866120	109866121	G	A	37	GENIC	homozygous	119684708
3	109866121	109866122	A	G	37	GENIC	homozygous	119684709
3	109866165	109866166	C	A	31	GENIC	homozygous	119684710
3	109866166	109866167	A	C	30	GENIC	homozygous	112428519
3	109866356	109866357	A	G	23	GENIC	homozygous	111671544
3	109866952	109866953	A	T	19	GENIC	homozygous	111671546
3	109867388	109867389	G	C	33	GENIC	homozygous	111671556
3	109867403	109867404	A	T	37	GENIC	homozygous	111671558
3	109867927	109867928	G	T	34	GENIC	homozygous	111671560
3	109868819	109868820	T	C	45	GENIC	homozygous	111671562
3	109869141	109869142	A	G	24	GENIC	homozygous	111671564
3	109869509	109869510	A	T	29	GENIC	homozygous	111671565
3	109871040	109871041	A	G	29	GENIC	homozygous	111671569
3	109871405	109871406	C	A	36	GENIC	homozygous	111671571
3	109871807	109871808	C	T	37	GENIC	homozygous	112138639
3	109871811	109871812	G	A	38	GENIC	homozygous	111671573
3	109872310	109872311	G	A	12	GENIC	homozygous	111671575