chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	45831731	45831732	A	T	55	GENIC	possibly homozygous	147460130
10	45832564	45832565	A	G	56	GENIC	homozygous	142239627
10	45834929	45834930	C	T	49	GENIC	homozygous	145739771
10	45835081	45835082	G	A	75	GENIC	homozygous	142239640
10	45839642	45839643	A	T	67	GENIC	homozygous	142239649
10	45841901	45841902	C	A	72	GENIC	homozygous	147460131
10	45845536	45845537	C	T	62	GENIC	homozygous	146956098
10	45845893	45845894	T	C	58	GENIC	homozygous	146956099
10	45847757	45847758	T	G	53	GENIC	homozygous	147460132
10	45847891	45847892	G	T	72	GENIC	homozygous	147460133
10	45848067	45848068	T	C	44	GENIC	homozygous	142239654
10	45848220	45848221	A	C	34	GENIC	homozygous	147460134
10	45848467	45848493	CTGTTACACAGAGAAACCCTATCTTA		52	GENIC	homozygous	142201638
10	45848498	45848499	G	A	52	GENIC	homozygous	142239657
10	45848972	45848972		TTTCAAAAGGACCA	51	GENIC	homozygous	142201639
10	45850593	45850594	G	A	57	GENIC	homozygous	142239660
10	45852780	45852781	G	C	29	GENIC	homozygous	142239661
10	45854958	45854959	G	A	44	GENIC	homozygous	146956103
10	45844574	45844575	T		59	GENIC	possibly homozygous	147457630