chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	9151959	9151960	G	A	23	GENIC	homozygous	45679249
20	9152909	9152910	T	C	10	GENIC	homozygous	45679250
20	9152975	9152976	A	C	11	GENIC	homozygous	45421921
20	9153037	9153038	C	T	27	GENIC	homozygous	45421923
20	9153092	9153093	C	G	22	GENIC	homozygous	45421925
20	9153145	9153146	C	G	27	GENIC	homozygous	45421926
20	9153154	9153155	G	GA	29	GENIC	homozygous	45421928
20	9153158	9153159	T	C	29	GENIC	homozygous	45421930
20	9153213	9153214	T	-	31	GENIC	homozygous	45737587
20	9153214	9153215	T	G	34	GENIC	homozygous	45819160
20	9153667	9153669	GG	--	10	GENIC	homozygous	45679251
20	9154219	9154221	AC	--	12	GENIC	homozygous	45974314
20	9155046	9155047	A	C	30	GENIC	homozygous	45679253
20	9156882	9156883	A	AC	11	GENIC	homozygous	45421973
20	9157913	9157914	T	A	32	GENIC	homozygous	45679266
20	9158190	9158191	C	CAA	21	GENIC	homozygous	45622471
20	9158947	9158948	G	C	33	GENIC	possibly homozygous	45421987
20	9158958	9158959	G	GTTT	18	GENIC	homozygous	45900283
20	9159504	9159505	C	CT	7	GENIC	homozygous	45841636
20	9160389	9160390	G	A	19	GENIC	homozygous	45974315
20	9160705	9160706	T	A	16	GENIC	homozygous	45422013
20	9162352	9162354	AC	--	11	GENIC	homozygous	45422021
20	9163307	9163308	C	T	9	GENIC	homozygous	45679269
20	9163962	9163964	AC	--	17	GENIC	homozygous	45422041
20	9165751	9165752	A	C	27	GENIC	homozygous	45422050
20	9168223	9168224	G	GTGCTTGCTAGGCAAGCGCTCTACCACTGAGCTAAATC	1	GENIC	homozygous	45891259
20	9166205	9166206	G	-	8	GENIC	homozygous	45863521