chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	32666616	32666617	G	A	56	GENIC	homozygous	52566406
8	32667177	32667178	G	A	58	GENIC	possibly homozygous	52566410
8	32667203	32667205	TT	--	5	GENIC	homozygous	52952789
8	32667222	32667223	T	C	58	GENIC	homozygous	52566413
8	32667363	32667364	C	G	71	GENIC	homozygous	52566416
8	32667456	32667457	T	C	48	GENIC	homozygous	52566422
8	32667527	32667528	T	-	45	GENIC	homozygous	52566425
8	32668262	32668263	T	TA	46	GENIC	homozygous	52566428
8	32668314	32668315	G	T	39	GENIC	heterozygous	52566431
8	32668314	32668315	G	GT	28	GENIC	possibly homozygous	52566434
8	32668325	32668326	C	T	43	GENIC	heterozygous	52566437
8	32668757	32668758	A	AG	78	GENIC	homozygous	52952791
8	32669348	32669349	G	C	64	GENIC	homozygous	52952793
8	32669797	32669813	CAACCAAACAAACAAA	----------------	37	GENIC	homozygous	52566443
8	32670118	32670121	AAA	---	35	GENIC	heterozygous	52952795
8	32670119	32670121	AA	--	35	GENIC	possibly homozygous	52952797
8	32671157	32671158	T	-	2	GENIC	homozygous	52952799
8	32671171	32671172	C	-	30	GENIC	heterozygous	52566449
8	32671756	32671757	T	A	65	GENIC	homozygous	52952801
8	32672362	32672363	G	A	23	GENIC	homozygous	52566452
8	32674269	32674270	C	T	72	GENIC	homozygous	52952803
8	32676065	32676066	C	T	63	GENIC	homozygous	52952805
8	32676172	32676173	A	G	35	GENIC	possibly homozygous	52952807
8	32676190	32676191	C	CAA	11	GENIC	heterozygous	52952809
8	32676190	32676191	C	CA	11	GENIC	heterozygous	52952811
8	32676312	32676313	T	C	44	GENIC	homozygous	52952813
8	32676460	32676461	C	T	44	GENIC	homozygous	52952815
8	32676732	32676733	T	C	59	GENIC	homozygous	52566458
8	32676821	32676822	G	A	61	GENIC	homozygous	52952817
8	32676885	32676886	G	GTTT	8	GENIC	heterozygous	52566461
8	32676896	32676897	G	-	32	GENIC	homozygous	52566464
8	32677114	32677117	TTT	---	60	GENIC	homozygous	52566467
8	32677373	32677374	A	T	62	GENIC	homozygous	52952819
8	32677668	32677669	G	GCTACTTTCT	27	GENIC	homozygous	52566473