chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	90140314	90140315	G	A	13	GENIC	heterozygous	52574944
10	90141789	90141790	T	C	31	GENIC	homozygous	51735970
10	90141831	90141832	T	-	2	GENIC	homozygous	51537752
10	90142716	90142717	C	CA	1	GENIC	homozygous	52396027
10	90143606	90143607	A	G	21	GENIC	possibly homozygous	51735976
10	90145193	90145194	G	T	14	GENIC	possibly homozygous	52574947
10	90145707	90145708	C	-	6	INTERGENIC	homozygous	51537755
10	90145773	90145774	A	T	15	INTERGENIC	possibly homozygous	52574950
10	90148162	90148163	C	T	31	INTERGENIC	possibly homozygous	51537757
10	90148355	90148357	CA	--	14	INTERGENIC	possibly homozygous	51537758
10	90155284	90155285	C	T	24	INTERGENIC	possibly homozygous	51537773
10	90155821	90155822	A	AG	2	INTERGENIC	heterozygous	52396049
10	90156930	90156931	C	T	3	INTERGENIC	homozygous	52396051
10	90157833	90157834	A	G	15	INTERGENIC	possibly homozygous	51537778
10	90161305	90161306	C	CA	5	INTERGENIC	heterozygous	52396069
10	90163477	90163478	A	G	16	INTERGENIC	possibly homozygous	51537791
10	90164263	90164264	C	T	28	INTERGENIC	homozygous	51537793
10	90164578	90164579	A	AC	18	INTERGENIC	possibly homozygous	51537794
10	90166954	90166955	C	T	16	GENIC	homozygous	52574952
10	90168577	90168578	T	C	21	GENIC	homozygous	51537799