chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	46154590	46154591	A	G	32	GENIC	homozygous	51444202
10	46154908	46154909	A	T	21	GENIC	homozygous	51874917
10	46155760	46155761	C	T	26	GENIC	homozygous	51874919
10	46157313	46157314	T	C	18	GENIC	homozygous	51874922
10	46157742	46157743	T	C	28	GENIC	homozygous	51874925
10	46157999	46158000	C	T	36	GENIC	homozygous	51874928
10	46158275	46158276	G	A	24	GENIC	homozygous	51444207
10	46158502	46158503	T	C	32	GENIC	homozygous	51444208
10	46158511	46158512	T	G	31	GENIC	homozygous	51444209
10	46159503	46159504	C	G	32	GENIC	homozygous	51636700
10	46159445	46159446	A	G	25	GENIC	homozygous	51874931
10	46161264	46161265	A	AC	17	GENIC	homozygous	51636702
10	46163224	46163227	AAG	---	31	INTERGENIC	homozygous	51444210
10	46164492	46164493	C	T	20	INTERGENIC	homozygous	51444211
10	46164526	46164527	A	-	13	INTERGENIC	possibly homozygous	51444212
10	46166767	46166768	T	C	19	INTERGENIC	homozygous	51444215
10	46166782	46166783	C	G	18	INTERGENIC	homozygous	51874934
10	46167048	46167049	A	AG	19	INTERGENIC	homozygous	51444216
10	46167208	46167209	G	GGGGA	20	INTERGENIC	homozygous	51444217
10	46167296	46167297	T	C	34	INTERGENIC	homozygous	51444218
10	46168328	46168329	A	AGG	6	INTERGENIC	homozygous	51874936
10	46170085	46170086	G	A	27	INTERGENIC	homozygous	51874939