chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	108396131	108396132	A	C	22	GENIC	homozygous	116715794
10	108397121	108397122	A	G	45	GENIC	homozygous	116715796
10	108397668	108397669	C	T	34	GENIC	homozygous	116715798
10	108398796	108398797	A	T	30	GENIC	homozygous	116715800
10	108399027	108399028	G	A	50	GENIC	homozygous	116715802
10	108399555	108399556	G	C	22	GENIC	homozygous	116715804
10	108399783	108399784	C	T	51	GENIC	homozygous	116715806
10	108400024	108400025	C	T	24	GENIC	homozygous	116715808
10	108400208	108400209	A	G	30	GENIC	homozygous	116715810
10	108400410	108400411	C	G	40	GENIC	homozygous	117313442
10	108401178	108401179	T	C	35	GENIC	homozygous	116715812
10	108401310	108401311	C	T	24	GENIC	heterozygous	118071035
10	108401602	108401603	T	C	31	GENIC	homozygous	116715814
10	108401854	108401855	A	T	52	GENIC	homozygous	116715816
10	108401948	108401949	T	C	25	GENIC	homozygous	116715818
10	108402722	108402723	G	A	39	GENIC	homozygous	116715820
10	108403313	108403314	A	C	37	GENIC	homozygous	116715822
10	108404211	108404212	A	G	17	GENIC	possibly homozygous	117297533
10	108404485	108404486	C	A	23	GENIC	heterozygous	118012864
10	108407888	108407889	T	C	30	GENIC	homozygous	116715826
10	108407915	108407916	G	T	32	GENIC	homozygous	116715828
10	108409903	108409904	C	A	34	GENIC	homozygous	116715830
10	108410467	108410468	A	G	30	GENIC	homozygous	116715832
10	108411514	108411515	C	T	35	GENIC	homozygous	116715834
10	108412793	108412794	G	A	42	GENIC	homozygous	116715836