chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	30756018	30756019	A	AGGTTT	40	GENIC	homozygous	50715679
11	30756563	30756564	G	-	14	GENIC	possibly homozygous	50715681
11	30756875	30756876	A	AC	15	GENIC	possibly homozygous	50715683
11	30757130	30757132	TT	--	8	GENIC	heterozygous	50715686
11	30757131	30757132	T	-	8	GENIC	heterozygous	50877161
11	30757224	30757225	C	T	14	GENIC	homozygous	50916918
11	30757374	30757375	T	G	22	GENIC	homozygous	50916919
11	30757965	30757966	T	-	11	GENIC	possibly homozygous	50715688
11	30758170	30758171	C	T	32	GENIC	homozygous	50916920
11	30758600	30758601	G	C	30	GENIC	homozygous	50916921
11	30759034	30759035	C	T	15	GENIC	homozygous	50916922
11	30760656	30760657	A	G	26	GENIC	homozygous	50715689
11	30760802	30760803	A	C	19	GENIC	homozygous	50715690
11	30761912	30761913	T	TG	15	GENIC	homozygous	50715691
11	30762108	30762109	T	A	22	GENIC	homozygous	50916923
11	30762741	30762742	A	G	35	GENIC	homozygous	50715692
11	30763073	30763074	G	T	18	GENIC	homozygous	50715693
11	30763705	30763706	C	-	18	GENIC	homozygous	50916924
11	30763869	30763870	C	T	20	GENIC	homozygous	50916925
11	30763913	30763914	A	-	21	GENIC	possibly homozygous	50916926
11	30764052	30764053	C	T	35	GENIC	homozygous	50916927
11	30765173	30765174	A	C	38	GENIC	homozygous	50715695
11	30765215	30765216	T	C	41	GENIC	homozygous	50916928
11	30766502	30766505	AAT	---	11	GENIC	homozygous	50916929
11	30766819	30766820	C	T	25	GENIC	homozygous	50715697
11	30767328	30767329	A	T	16	GENIC	homozygous	50916931