chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	91030656	91030657	C	G	8	GENIC	homozygous	50864861
11	91030905	91030906	T	C	8	GENIC	homozygous	50864862
11	91030942	91030943	T	C	8	GENIC	homozygous	50975178
11	91032422	91032423	A	-	8	GENIC	possibly homozygous	50864864
11	91033756	91033758	AC	--	16	GENIC	heterozygous	51230240
11	91034571	91034572	C	T	26	GENIC	homozygous	50864866
11	91034797	91034798	A	ACCC	27	GENIC	homozygous	50864867
11	91034798	91034799	A	AATGAC	27	GENIC	homozygous	50864869
11	91035256	91035257	T	C	20	GENIC	homozygous	50864870
11	91035386	91035387	G	T	20	GENIC	homozygous	50864871
11	91035734	91035735	T	TTCTC	15	GENIC	homozygous	50864872
11	91035938	91035939	A	G	16	GENIC	homozygous	50864873
11	91036082	91036083	C	T	17	GENIC	homozygous	50864874
11	91032698	91032699	C	T	17	GENIC	homozygous	51135742