chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	90141831	90141832	T	-	1	GENIC	homozygous	51537752
10	90148122	90148123	C	T	7	INTERGENIC	homozygous	51537756
10	90148162	90148163	C	T	15	INTERGENIC	possibly homozygous	51537757
10	90148355	90148357	CA	--	5	INTERGENIC	homozygous	51537758
10	90148583	90148584	T	G	5	INTERGENIC	homozygous	51537761
10	90151784	90151785	C	T	17	INTERGENIC	homozygous	51537764
10	90152688	90152689	C	T	15	INTERGENIC	homozygous	51537767
10	90153639	90153640	A	AGAGG	4	INTERGENIC	heterozygous	51537768
10	90154559	90154560	A	T	1	INTERGENIC	homozygous	51537771
10	90154884	90154885	G	GA	2	INTERGENIC	homozygous	51537772
10	90155284	90155285	C	T	10	INTERGENIC	possibly homozygous	51537773
10	90156492	90156493	A	G	7	INTERGENIC	homozygous	51537776
10	90157761	90157762	T	TA	1	INTERGENIC	homozygous	51537777
10	90157833	90157834	A	G	5	INTERGENIC	homozygous	51537778
10	90158046	90158047	A	G	14	INTERGENIC	possibly homozygous	51537780
10	90161001	90161002	C	T	9	INTERGENIC	possibly homozygous	51537785
10	90161035	90161036	G	C	9	INTERGENIC	homozygous	51537786
10	90161301	90161302	A	-	6	INTERGENIC	homozygous	51537787
10	90161306	90161307	A	C	9	INTERGENIC	homozygous	52508365
10	90161610	90161611	G	T	11	INTERGENIC	homozygous	51537788
10	90163237	90163239	AA	--	6	INTERGENIC	heterozygous	51537790
10	90163477	90163478	A	G	7	INTERGENIC	possibly homozygous	51537791
10	90163904	90163911	GTGCCCT	-------	1	INTERGENIC	homozygous	51537792
10	90164263	90164264	C	T	23	INTERGENIC	possibly homozygous	51537793
10	90164578	90164579	A	AC	7	INTERGENIC	homozygous	51537794
10	90165852	90165853	T	TC	5	GENIC	heterozygous	51537795
10	90166447	90166448	A	AT	3	GENIC	heterozygous	51537797
10	90167979	90167980	C	T	8	GENIC	possibly homozygous	51537798
10	90168577	90168578	T	C	8	GENIC	homozygous	51537799