chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	72749950	72749951	A	G	14	GENIC	homozygous	116052794
11	72750067	72750068	T	A	17	GENIC	homozygous	115987547
11	72750487	72750488	T	G	22	GENIC	homozygous	116105831
11	72750687	72750688	G	C	21	GENIC	homozygous	116105832
11	72751615	72751616	C	G	20	GENIC	homozygous	115899866
11	72755007	72755008	G	A	18	GENIC	homozygous	115899870
11	72825015	72825016	C	T	18	GENIC	homozygous	116110601
11	72825085	72825086	G	A	10	GENIC	homozygous	116110602
11	73019534	73019535	A	G	15	GENIC	homozygous	115987553
11	73024542	73024543	G	C	18	GENIC	homozygous	115987559
11	73024644	73024645	C	T	21	GENIC	homozygous	116105833
11	73024752	73024753	T	C	27	GENIC	homozygous	116105834
11	73025130	73025131	C	T	14	GENIC	homozygous	116105835
11	73026010	73026011	G	A	14	GENIC	homozygous	116105836
11	73026898	73026899	G	A	18	GENIC	homozygous	116105837
11	73027390	73027391	C	T	25	GENIC	homozygous	116105838
11	73027899	73027900	T	C	17	GENIC	homozygous	116105839
11	73028455	73028456	T	C	31	GENIC	homozygous	115987565
11	73028706	73028707	G	A	33	GENIC	homozygous	116105840
11	73030017	73030018	A	C	16	GENIC	homozygous	115899878
11	73030018	73030019	C	A	16	GENIC	homozygous	115899880
11	73031282	73031283	T	G	20	GENIC	homozygous	115987567
11	73033868	73033869	T	C	18	GENIC	homozygous	115987569