chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	54572612	54572613	C	T	16	GENIC	homozygous	56154970
5	54572672	54572673	C	T	20	GENIC	homozygous	56217421
5	54572785	54572786	C	CG	22	GENIC	homozygous	56154974
5	54573111	54573112	C	T	19	GENIC	homozygous	56217423
5	54572855	54572860	GTGTG	-----	9	GENIC	homozygous	56416399
5	54572859	54572860	G	GACA	8	GENIC	homozygous	56416401
5	54574349	54574352	CCC	---	34	GENIC	homozygous	56416403
5	54574358	54574359	C	CAA	35	GENIC	homozygous	56416405
5	54576488	54576489	G	A	25	GENIC	homozygous	56154988
5	54576818	54576819	G	A	29	GENIC	homozygous	56217424
5	54577111	54577112	T	C	19	GENIC	homozygous	56154992
5	54577327	54577328	T	-	10	GENIC	homozygous	56154994
5	54577328	54577329	T	A	10	GENIC	homozygous	56347408
5	54577578	54577579	G	A	9	GENIC	homozygous	55380728
5	54578319	54578320	A	C	20	GENIC	homozygous	55380729
5	54578619	54578627	AACATAGT	--------	15	GENIC	homozygous	55380730
5	54579198	54579199	A	G	18	GENIC	homozygous	56154996
5	54579838	54579839	A	-	10	GENIC	homozygous	56154998
5	54579865	54579866	T	A	16	GENIC	homozygous	55380731
5	54580124	54580125	A	T	16	GENIC	homozygous	56155001
5	54580227	54580228	G	GT	33	GENIC	homozygous	56217425
5	54580395	54580396	C	T	15	GENIC	homozygous	56155005
5	54580453	54580454	C	T	22	GENIC	homozygous	56155009
5	54580512	54580516	TGTG	----	19	GENIC	homozygous	56155011
5	54580609	54580610	A	T	20	GENIC	homozygous	56155013
5	54581640	54581642	TA	--	20	GENIC	homozygous	55380733
5	54581845	54581846	G	GT	21	GENIC	possibly homozygous	56155017
5	54584922	54584923	C	T	31	GENIC	homozygous	56217426
5	54576637	54576638	G	GA	11	GENIC	homozygous	55877725
5	54583212	54583213	A	T	19	GENIC	homozygous	56010679
5	54583398	54583399	T	-	19	GENIC	homozygous	56010681