chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	11466141	11466142	G	T	12	GENIC	homozygous	138725154
10	11466427	11466428	G	C	19	GENIC	homozygous	138725155
10	11466749	11466750	G	C	16	GENIC	homozygous	138725156
10	11467690	11467691	G	A	16	GENIC	homozygous	138725157
10	11467706	11467707	C	A	14	GENIC	homozygous	138725158
10	11470755	11470756	G	A	21	GENIC	homozygous	138725159
10	11473182	11473183	C	T	24	GENIC	homozygous	138725160
10	11473679	11473680	G	C	23	GENIC	homozygous	138725161
10	11475678	11475679	C	T	22	GENIC	homozygous	138725162
10	11477574	11477575	G	T	11	GENIC	homozygous	138725163
10	11478183	11478183		A	16	GENIC	homozygous	138668847
10	11482552	11482554	TG		13	GENIC	homozygous	138668848
10	11485648	11485649	A	G	13	GENIC	homozygous	138725164
10	11487063	11487064	T	C	19	GENIC	homozygous	138725165
10	11487076	11487077	T	G	19	GENIC	homozygous	138725166
10	11488551	11488552	T	C	16	GENIC	homozygous	138725167
10	11489959	11489960	G	A	19	GENIC	homozygous	138725168
10	11490759	11490760	T	G	15	GENIC	homozygous	138725169
10	11493966	11493967	A	G	18	GENIC	homozygous	138725170
10	11497504	11497505	A	G	18	GENIC	homozygous	138725171
10	11498278	11498279	A	C	21	GENIC	homozygous	138725172
10	11498701	11498702	T	C	17	GENIC	homozygous	138725173