chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	91222132	91222133	G	A	37	GENIC	homozygous	51539296
10	91223257	91223258	G	A	33	GENIC	homozygous	52968568
10	91225077	91225078	T	TCCCTTCAGGATGTCTTTCTGCTGTGTCTTCCTG	37	GENIC	homozygous	52323341
10	91227627	91227628	T	TACAC	3	GENIC	heterozygous	52968570
10	91228782	91228784	AA	--	29	GENIC	homozygous	51539314
10	91230347	91230348	T	C	30	GENIC	homozygous	52968572
10	91233857	91233858	A	G	19	GENIC	possibly homozygous	52166073
10	91233989	91234001	AACCAACCAACC	------------	22	GENIC	homozygous	52397299
10	91234833	91234834	G	-	57	GENIC	homozygous	52166075
10	91243927	91243930	AAC	---	5	GENIC	homozygous	51539344
10	91244176	91244180	AGAG	----	8	GENIC	heterozygous	52968574
10	91244178	91244180	AG	--	8	GENIC	heterozygous	52913023
10	91245955	91245957	AA	--	4	GENIC	heterozygous	51539350
10	91245956	91245957	A	-	4	GENIC	heterozygous	52809351
10	91249631	91249632	T	C	18	GENIC	homozygous	51539353
10	91256101	91256102	A	T	65	GENIC	homozygous	52968576
10	91258287	91258288	C	CGA	11	GENIC	heterozygous	52809355
10	91261265	91261266	C	CAA	4	GENIC	heterozygous	51539368
10	91261265	91261266	C	CA	4	GENIC	heterozygous	52651056
10	91262199	91262201	AC	--	5	GENIC	heterozygous	52968579
10	91265096	91265111	AAAAAAAAAAAAAAA	---------------	18	GENIC	homozygous	52968581