chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	89997110	89997111	T	-	6	GENIC	homozygous	50898703
11	89997126	89997127	T	-	6	GENIC	homozygous	50898704
11	89997128	89997129	T	-	6	GENIC	homozygous	50898705
11	89999959	89999963	ACAC	----	14	GENIC	homozygous	50974579
11	90001198	90001200	AC	--	18	GENIC	homozygous	51034955
11	90001478	90001479	C	T	30	GENIC	homozygous	51034956
11	90001570	90001571	T	C	45	GENIC	homozygous	51034957
11	90003554	90003555	T	C	25	GENIC	homozygous	51034958
11	90004074	90004075	T	C	13	GENIC	homozygous	51034959
11	90004120	90004121	G	T	17	GENIC	possibly homozygous	51034960
11	90004519	90004520	C	G	35	GENIC	homozygous	51034961
11	90005630	90005631	G	C	36	GENIC	homozygous	51034962
11	90007939	90007940	T	C	50	GENIC	homozygous	51034963
11	90008068	90008069	T	A	18	GENIC	homozygous	51034964
11	90008935	90008936	G	A	34	GENIC	possibly homozygous	51034965
11	90009024	90009025	T	C	36	GENIC	homozygous	51034966
11	90009443	90009444	C	CCT	15	GENIC	heterozygous	51034967
11	90009984	90009985	T	C	31	GENIC	possibly homozygous	51034968
11	90011174	90011175	A	AT	25	GENIC	possibly homozygous	51034969
11	90009443	90009444	C	CCCT	15	GENIC	possibly homozygous	50863001
11	90009434	90009435	G	GC	15	GENIC	homozygous	50863000