chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	34217999	34218000	A	G	23	GENIC	homozygous	55290850
5	34218028	34218029	A	T	25	GENIC	homozygous	55990653
5	34218208	34218209	T	A	38	GENIC	homozygous	55290851
5	34218230	34218231	G	C	38	GENIC	homozygous	55990654
5	34218723	34218724	T	C	42	GENIC	homozygous	55290852
5	34218876	34218877	G	-	8	GENIC	homozygous	55990655
5	34218886	34218887	A	G	14	GENIC	homozygous	55290854
5	34218922	34218924	AT	--	16	GENIC	homozygous	55290855
5	34219252	34219253	A	AT	40	GENIC	homozygous	55290856
5	34219262	34219263	C	CT	39	GENIC	homozygous	55290857
5	34220052	34220053	C	T	47	GENIC	possibly homozygous	55290860
5	34220682	34220683	G	A	42	GENIC	homozygous	55990656
5	34220967	34220968	G	T	53	GENIC	homozygous	55290861
5	34222996	34222997	G	GT	40	GENIC	possibly homozygous	55869572
5	34224137	34224138	C	T	27	GENIC	homozygous	55990657
5	34226461	34226462	G	GT	38	GENIC	homozygous	55990658
5	34227395	34227396	T	C	23	GENIC	homozygous	55290870
5	34229196	34229197	C	CA	6	GENIC	heterozygous	55290873
5	34229887	34229888	A	AAT	42	GENIC	possibly homozygous	55290875
5	34230838	34230839	G	A	35	GENIC	homozygous	55290877
5	34231747	34231748	A	-	11	GENIC	possibly homozygous	55290880
5	34231747	34231748	A	AAGG	11	GENIC	heterozygous	55290881
5	34231752	34231753	G	A	11	GENIC	possibly homozygous	55290882
5	34231934	34231935	C	T	32	GENIC	homozygous	55290883
5	34234163	34234164	G	A	32	GENIC	homozygous	55990659
5	34236724	34236725	T	C	66	GENIC	homozygous	55290888
5	34237943	34237944	T	-	23	GENIC	heterozygous	55990660