chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	89374886	89374887	C	T	58	GENIC	homozygous	51732888
10	89374935	89374936	T	G	59	GENIC	homozygous	51732890
10	89374985	89374986	T	C	51	GENIC	homozygous	51732892
10	89375268	89375269	A	C	28	GENIC	homozygous	51732894
10	89375274	89375275	C	T	29	GENIC	possibly homozygous	51732896
10	89375458	89375459	G	A	34	GENIC	possibly homozygous	51732898
10	89375498	89375499	G	T	42	GENIC	possibly homozygous	51732900
10	89375795	89375796	T	G	33	GENIC	homozygous	51732902
10	89376025	89376029	TTTC	----	28	GENIC	homozygous	51732904
10	89376059	89376060	C	G	39	GENIC	homozygous	51732906
10	89376209	89376210	A	AT	27	GENIC	homozygous	51732908
10	89376230	89376231	G	A	28	GENIC	possibly homozygous	51732912
10	89376457	89376458	A	C	33	GENIC	homozygous	51732914
10	89376676	89376677	G	C	44	GENIC	possibly homozygous	51732916
10	89377603	89377613	TTTTTTTTTT	----------	3	GENIC	homozygous	52206492