chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	61382386	61382386		CGACTCGCGACT	62	GENIC	homozygous	128189934
5	61382398	61382399	T	A	66	GENIC	homozygous	113828333
5	61383526	61383527	C	T	60	GENIC	homozygous	113828335
5	61383854	61383855	C	T	45	GENIC	homozygous	113828337
5	61383855	61383856	A	G	45	GENIC	homozygous	113828339
5	61383879	61383879		G	52	GENIC	homozygous	128189935
5	61383922	61383923	C	T	51	GENIC	homozygous	113828341
5	61384389	61384389		G	44	GENIC	homozygous	128189936
5	61384566	61384567	T	G	51	GENIC	homozygous	113828343
5	61384583	61384584	G	A	54	GENIC	homozygous	113828345
5	61385007	61385008	T	C	59	GENIC	homozygous	113828347
5	61385388	61385389	G	A	38	GENIC	homozygous	113828349
5	61385583	61385584	A	G	52	GENIC	homozygous	113828351
5	61385862	61385863	G	A	61	GENIC	homozygous	113828353
5	61386720	61386721	A	G	55	GENIC	homozygous	113828365
5	61385925	61385926	A	G	50	GENIC	homozygous	113828355
5	61385952	61385953	T	C	51	GENIC	homozygous	113828357
5	61386180	61386181	T	C	62	GENIC	homozygous	113828359
5	61386457	61386458	A	G	58	GENIC	homozygous	113828361
5	61386459	61386460	T	C	60	GENIC	homozygous	113828363
5	61386860	61386861	G	A	48	GENIC	homozygous	113828367
5	61387057	61387058	T	C	53	GENIC	homozygous	113828369
5	61387167	61387168	T	C	31	GENIC	homozygous	113828371