chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	108396131	108396132	A	C	7	GENIC	homozygous	116715794
10	108397121	108397122	A	G	16	GENIC	homozygous	116715796
10	108397668	108397669	C	T	20	GENIC	possibly homozygous	116715798
10	108398796	108398797	A	T	13	GENIC	homozygous	116715800
10	108399027	108399028	G	A	21	GENIC	homozygous	116715802
10	108399555	108399556	G	C	20	GENIC	homozygous	116715804
10	108399783	108399784	C	T	25	GENIC	homozygous	116715806
10	108400024	108400025	C	T	15	GENIC	homozygous	116715808
10	108400208	108400209	A	G	17	GENIC	homozygous	116715810
10	108401178	108401179	T	C	20	GENIC	homozygous	116715812
10	108401602	108401603	T	C	10	GENIC	homozygous	116715814
10	108401854	108401855	A	T	16	GENIC	homozygous	116715816
10	108401948	108401949	T	C	9	GENIC	homozygous	116715818
10	108402722	108402723	G	A	8	GENIC	homozygous	116715820
10	108403313	108403314	A	C	5	GENIC	homozygous	116715822
10	108404004	108404005	T	C	2	GENIC	homozygous	117261444
10	108404009	108404010	T	C	4	GENIC	heterozygous	117261446
10	108407888	108407889	T	C	25	GENIC	homozygous	116715826
10	108407915	108407916	G	T	19	GENIC	homozygous	116715828
10	108409903	108409904	C	A	12	GENIC	homozygous	116715830
10	108410467	108410468	A	G	17	GENIC	homozygous	116715832
10	108411514	108411515	C	T	11	GENIC	homozygous	116715834
10	108412793	108412794	G	A	8	GENIC	homozygous	116715836