chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	110498369	110498370	A	C	2	GENIC	homozygous	119702348
3	110499789	110499790	G	A	24	GENIC	homozygous	111672865
3	110500108	110500109	T	C	6	GENIC	homozygous	111672878
3	110503504	110503505	T	C	21	GENIC	homozygous	112138916
3	110504763	110504764	A	T	27	GENIC	homozygous	112138917
3	110504969	110504970	G	A	35	GENIC	possibly homozygous	112138918
3	110505507	110505508	T	C	29	GENIC	homozygous	112003679
3	110505750	110505751	C	T	20	GENIC	homozygous	111672884
3	110505866	110505867	T	C	15	GENIC	homozygous	112003681
3	110507116	110507117	G	T	24	GENIC	homozygous	112138919
3	110511887	110511888	A	G	21	GENIC	homozygous	112003695
3	110509767	110509768	G	A	19	GENIC	homozygous	112003689
3	110510216	110510217	A	T	17	GENIC	homozygous	112003691
3	110510613	110510614	G	A	23	GENIC	homozygous	111672885
3	110513094	110513095	C	G	22	GENIC	homozygous	111672887
3	110514906	110514907	G	A	31	GENIC	homozygous	112138920
3	110514954	110514955	G	C	38	GENIC	homozygous	112003699
3	110515246	110515247	G	C	24	GENIC	homozygous	112003703
3	110516650	110516651	C	T	29	GENIC	homozygous	112138921
3	110516979	110516980	T	C	21	GENIC	homozygous	112003707