chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	110498421	110498422	C	A	1	GENIC	homozygous	127988640
3	110498423	110498424	G		1	GENIC	homozygous	127918108
3	110498430	110498431	C		3	GENIC	homozygous	127918109
3	110498441	110498444	CTG		5	GENIC	homozygous	127918110
3	110499789	110499790	G	A	33	GENIC	homozygous	111672865
3	110500027	110500028	A	T	22	GENIC	homozygous	111672867
3	110500044	110500045	T	A	22	GENIC	homozygous	111672869
3	110500047	110500048	G	T	22	GENIC	homozygous	111672871
3	110500056	110500057	G	T	20	GENIC	homozygous	111672873
3	110500063	110500064	C	G	19	GENIC	homozygous	111672874
3	110500071	110500071		TG	17	GENIC	homozygous	129891038
3	110500073	110500075	CT		17	GENIC	homozygous	129891039
3	110500094	110500095	A	C	12	GENIC	homozygous	111672876
3	110500108	110500109	T	C	10	GENIC	homozygous	111672878
3	110500160	110500161	G	A	3	GENIC	homozygous	119914232
3	110500164	110500165	G	A	3	GENIC	homozygous	132052030
3	110500168	110500169	G	A	1	GENIC	homozygous	132292916
3	110505507	110505508	T	C	32	GENIC	homozygous	112003679
3	110505750	110505751	C	T	19	GENIC	homozygous	111672884
3	110505866	110505867	T	C	23	GENIC	homozygous	112003681
3	110509767	110509768	G	A	18	GENIC	homozygous	112003689
3	110510216	110510217	A	T	17	GENIC	homozygous	112003691
3	110510613	110510614	G	A	25	GENIC	homozygous	111672885
3	110511887	110511888	A	G	13	GENIC	homozygous	112003695
3	110513094	110513095	C	G	20	GENIC	homozygous	111672887
3	110514954	110514955	G	C	23	GENIC	homozygous	112003699
3	110515246	110515247	G	C	31	GENIC	homozygous	112003703
3	110516650	110516651	C	T	40	GENIC	homozygous	112138921
3	110503458	110503459	C		13	GENIC	homozygous	127918112
3	110502928	110502929	C		16	GENIC	homozygous	130907811
3	110503504	110503505	T	C	23	GENIC	homozygous	112138916
3	110504763	110504764	A	T	23	GENIC	homozygous	112138917
3	110504969	110504970	G	A	13	GENIC	homozygous	112138918
3	110507116	110507117	G	T	19	GENIC	possibly homozygous	112138919
3	110516979	110516980	T	C	21	GENIC	homozygous	112003707