chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	54571627	54571628	A		52	GENIC	homozygous	142203467
10	54571787	54571788	A	G	46	GENIC	homozygous	142248119
10	54571902	54571903	A	G	50	GENIC	homozygous	142248120
10	54571908	54571909	A	G	49	GENIC	homozygous	142248121
10	54572277	54572278	A	G	63	GENIC	homozygous	142248122
10	54572353	54572354	A	G	51	GENIC	homozygous	142248123
10	54573945	54573946	G	A	48	GENIC	homozygous	142248124
10	54574810	54574811	G	T	26	GENIC	homozygous	142248125
10	54574863	54574864	T	G	27	GENIC	homozygous	142248126
10	54575699	54575701	TA		51	GENIC	homozygous	142203468
10	54575955	54575956	G	A	46	GENIC	homozygous	142248127
10	54576026	54576027	G	A	63	GENIC	homozygous	142248128
10	54576705	54576706	T	C	50	GENIC	homozygous	142248131
10	54576242	54576243	A	G	63	GENIC	homozygous	142248129
10	54576687	54576688	A	G	49	GENIC	homozygous	142248130
10	54577067	54577068	T	C	67	GENIC	homozygous	142248132
10	54577594	54577594		GAAG	42	GENIC	homozygous	142203469
10	54577780	54577781	A	G	52	GENIC	homozygous	142248133
10	54579099	54579100	G	C	27	GENIC	heterozygous	403286954
10	54579097	54579098	G		26	GENIC	heterozygous	403286951
10	54579097	54579098	G	C	26	GENIC	homozygous	403286952
10	54579099	54579100	G		27	GENIC	heterozygous	403286953
10	54579248	54579249	G	A	54	GENIC	homozygous	142248135
10	54579434	54579435	C	T	38	GENIC	homozygous	142248136
10	54579518	54579519	G	A	38	GENIC	homozygous	142248137
10	54580403	54580404	G	A	48	GENIC	homozygous	142248138