chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	17278060	17278061	T	C	44	GENIC	homozygous	139096708
12	17278086	17278089	AAT		42	GENIC	homozygous	139044004
12	17278208	17278209	C	T	47	GENIC	homozygous	139096709
12	17278218	17278219	T		47	GENIC	homozygous	139044005
12	17278367	17278368	G	C	50	GENIC	homozygous	139096710
12	17278583	17278584	C	G	51	GENIC	homozygous	139096711
12	17278805	17278806	T	G	45	GENIC	homozygous	139096712
12	17279079	17279082	AAG		18	GENIC	homozygous	139044006
12	17279556	17279557	T	C	43	GENIC	homozygous	139096713
12	17280654	17280655	C	A	62	GENIC	possibly homozygous	139096714
12	17281232	17281233	T	C	41	GENIC	homozygous	139096715
12	17281346	17281347	A	G	38	GENIC	homozygous	139096716
12	17281950	17281951	C	T	33	GENIC	homozygous	139096717
12	17281979	17281980	A	G	32	GENIC	homozygous	139096718
12	17282370	17282371	T	C	41	GENIC	homozygous	139096719
12	17282388	17282389	C	G	41	GENIC	homozygous	139096720
12	17282529	17282530	G	A	40	GENIC	homozygous	139096721
12	17282849	17282850	A	G	42	GENIC	homozygous	139096722
12	17283049	17283050	A	G	47	GENIC	homozygous	139096723
12	17283165	17283166	A	G	42	GENIC	homozygous	139096724
12	17283321	17283322	A	T	39	GENIC	homozygous	139096725
12	17283651	17283652	T	A	49	GENIC	homozygous	139096726
12	17283671	17283672	C	T	45	GENIC	homozygous	139096727
12	17283746	17283747	C	A	37	GENIC	homozygous	139096728
12	17283986	17283987	C	T	41	GENIC	homozygous	139096729
12	17284265	17284266	A	G	47	GENIC	homozygous	139096730