chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	134468818	134468819	C	T	46	GENIC	homozygous	114143968
5	134469169	134469170	A	G	46	GENIC	homozygous	114016894
5	134470622	134470623	G	A	44	GENIC	homozygous	114143969
5	134471241	134471242	G	A	39	GENIC	homozygous	114143970
5	134473057	134473058	G	C	20	GENIC	homozygous	114143982
5	134473137	134473138	T	G	28	GENIC	homozygous	114016900
5	134473998	134473999	A	G	45	GENIC	homozygous	114143983
5	134474383	134474384	G	A	49	GENIC	homozygous	114143984
5	134476413	134476414	A	G	39	GENIC	homozygous	114016903
5	134476884	134476885	C	T	33	GENIC	homozygous	114016904
5	134477258	134477259	G	A	45	GENIC	possibly homozygous	114143985
5	134477293	134477294	G	A	47	GENIC	homozygous	114143986
5	134477506	134477507	A	G	40	GENIC	homozygous	114016905
5	134477737	134477738	A	G	35	GENIC	homozygous	114143987
5	134471019	134471019		GGATGAGTCCTGTAGACTTT	35	GENIC	homozygous	128241780