chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	54571787	54571788	A	G	22	GENIC	homozygous	142248119
10	54571902	54571903	A	G	22	GENIC	homozygous	142248120
10	54571908	54571909	A	G	24	GENIC	homozygous	142248121
10	54572277	54572278	A	G	33	GENIC	homozygous	142248122
10	54572353	54572354	A	G	28	GENIC	homozygous	142248123
10	54573984	54573985	C	T	19	GENIC	homozygous	145741339
10	54574863	54574864	T	G	24	GENIC	homozygous	142248126
10	54576242	54576243	A	G	19	GENIC	homozygous	142248129
10	54576705	54576706	T	C	21	GENIC	homozygous	142248131
10	54577067	54577068	T	C	42	GENIC	homozygous	142248132
10	54577532	54577533	G	A	33	GENIC	homozygous	145741340
10	54577594	54577594		GAAG	28	GENIC	homozygous	142203469
10	54577780	54577781	A	G	19	GENIC	homozygous	142248133
10	54579518	54579519	G	A	38	GENIC	homozygous	142248137
10	54580403	54580404	G	A	35	GENIC	homozygous	142248138
10	54579097	54579098	G	C	8	GENIC	homozygous	403286952
10	54579097	54579098	G		8	GENIC	heterozygous	403286951