chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	32666616	32666617	G	A	15	GENIC	homozygous	52566406
8	32667177	32667178	G	A	21	GENIC	homozygous	52566410
8	32667222	32667223	T	C	19	GENIC	homozygous	52566413
8	32667363	32667364	C	G	20	GENIC	homozygous	52566416
8	32667456	32667457	T	C	19	GENIC	homozygous	52566422
8	32667527	32667528	T	-	13	GENIC	homozygous	52566425
8	32668262	32668263	T	TA	17	GENIC	homozygous	52566428
8	32668314	32668315	G	GT	18	GENIC	homozygous	52566434
8	32668757	32668758	A	AG	28	GENIC	homozygous	52952791
8	32669348	32669349	G	C	28	GENIC	homozygous	52952793
8	32669504	32669505	C	T	35	GENIC	homozygous	53098180
8	32669796	32669797	C	A	19	GENIC	heterozygous	53098181
8	32669797	32669813	CAACCAAACAAACAAA	----------------	23	GENIC	homozygous	52566443
8	32670118	32670121	AAA	---	19	GENIC	heterozygous	52952795
8	32670119	32670121	AA	--	19	GENIC	possibly homozygous	52952797
8	32670453	32670454	A	-	10	GENIC	homozygous	53098182
8	32671171	32671172	C	-	17	GENIC	heterozygous	52566449
8	32671756	32671757	T	A	24	GENIC	homozygous	52952801
8	32671878	32671879	G	A	20	GENIC	homozygous	53098183
8	32672214	32672215	C	G	23	GENIC	homozygous	53098184
8	32672312	32672313	C	T	22	GENIC	heterozygous	53098185
8	32672362	32672363	G	A	18	GENIC	homozygous	52566452
8	32672422	32672423	C	T	13	GENIC	homozygous	53098186
8	32676065	32676066	C	T	21	GENIC	homozygous	52952805
8	32676172	32676173	A	G	14	GENIC	homozygous	52952807
8	32676190	32676191	C	CAA	10	GENIC	heterozygous	52952809
8	32676190	32676191	C	CA	10	GENIC	heterozygous	52952811
8	32676312	32676313	T	C	22	GENIC	homozygous	52952813
8	32676732	32676733	T	C	28	GENIC	homozygous	52566458
8	32676821	32676822	G	A	20	GENIC	homozygous	52952817
8	32676896	32676897	G	-	21	GENIC	homozygous	52566464
8	32677114	32677117	TTT	---	9	GENIC	homozygous	52566467
8	32677373	32677374	A	T	14	GENIC	homozygous	52952819
8	32677668	32677669	G	GCTACTTTCT	6	GENIC	homozygous	52566473