chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	2794085	2794086	A	G	31	GENIC	homozygous	51063805
11	2794250	2794251	G	C	30	GENIC	homozygous	51063808
11	2794261	2794262	T	A	33	GENIC	homozygous	51063810
11	2794305	2794306	G	T	29	GENIC	homozygous	51063813
11	2794445	2794446	C	A	21	GENIC	homozygous	50631056
11	2794495	2794496	C	A	11	GENIC	homozygous	50631057
11	2794528	2794529	C	A	13	GENIC	homozygous	50631058
11	2794610	2794614	TGTG	----	10	GENIC	homozygous	51063815
11	2794985	2794986	C	T	15	GENIC	homozygous	51063818
11	2795062	2795063	C	T	23	GENIC	homozygous	51063820
11	2795132	2795133	T	A	23	GENIC	possibly homozygous	51063823
11	2795177	2795178	C	T	20	GENIC	possibly homozygous	51063826
11	2795369	2795370	C	A	22	GENIC	homozygous	51063828
11	2795398	2795399	G	A	22	GENIC	homozygous	51063831
11	2795609	2795610	G	A	22	GENIC	homozygous	51063833
11	2795776	2795777	G	A	32	GENIC	homozygous	51063835
11	2795854	2795855	C	T	42	GENIC	homozygous	51063838
11	2795873	2795874	A	C	45	GENIC	homozygous	51063840
11	2795943	2795944	G	T	40	GENIC	homozygous	51063843
11	2796145	2796146	T	-	25	GENIC	homozygous	51063845
11	2796174	2796175	T	C	29	GENIC	homozygous	51063847
11	2796361	2796362	G	T	18	GENIC	homozygous	51063850
11	2796784	2796786	TA	--	15	GENIC	homozygous	51063852
11	2796907	2796908	G	T	22	GENIC	homozygous	51063855
11	2796909	2796910	A	C	22	GENIC	homozygous	51063858
11	2797294	2797295	A	G	18	GENIC	homozygous	51063860