chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	2793935	2793936	C	T	8	GENIC	homozygous	51150371
11	2794085	2794086	A	G	9	GENIC	homozygous	51063805
11	2794250	2794251	G	C	16	GENIC	homozygous	51063808
11	2794528	2794529	C	A	9	GENIC	homozygous	50631058
11	2794596	2794598	TG	--	8	GENIC	homozygous	51208198
11	2794610	2794630	TGTGTGTGTGTGTGTGTGTG	--------------------	8	GENIC	homozygous	51208199
11	2794873	2794874	A	T	24	GENIC	homozygous	51150372
11	2795062	2795063	C	T	26	GENIC	possibly homozygous	51063820
11	2795208	2795209	C	G	20	GENIC	homozygous	51150373
11	2795369	2795370	C	A	18	GENIC	homozygous	51063828
11	2795609	2795610	G	A	27	GENIC	possibly homozygous	51063833
11	2795729	2795730	A	C	18	GENIC	homozygous	51150374
11	2795776	2795777	G	A	15	GENIC	homozygous	51063835
11	2796145	2796146	T	-	21	GENIC	homozygous	51063845
11	2796768	2796769	T	A	26	GENIC	homozygous	51150375
11	2796775	2796780	ATATT	-----	24	GENIC	homozygous	51150376
11	2796907	2796908	G	T	18	GENIC	homozygous	51063855
11	2796909	2796910	A	T	17	GENIC	homozygous	51150377
11	2797045	2797046	C	T	12	GENIC	homozygous	51150378