chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	65823611	65823612	T	C	22	GENIC	homozygous	51907207
10	65824182	65824183	G	A	23	GENIC	homozygous	51478384
10	65825587	65825588	T	C	14	GENIC	homozygous	51478387
10	65826041	65826042	G	C	20	GENIC	homozygous	51478389
10	65826464	65826465	G	GTGA	29	GENIC	homozygous	51478391
10	65826710	65826711	A	AT	14	GENIC	heterozygous	51478392
10	65826710	65826711	A	ATT	14	GENIC	heterozygous	51478393
10	65827625	65827626	T	C	18	GENIC	homozygous	51478394
10	65827927	65827929	AA	--	23	GENIC	homozygous	51478395
10	65828202	65828204	TT	--	14	GENIC	possibly homozygous	51907211
10	65828976	65828977	T	C	27	GENIC	homozygous	51478398
10	65829034	65829041	ATTGTGG	-------	22	GENIC	homozygous	51907213
10	65829124	65829125	T	C	28	GENIC	homozygous	51907215
10	65829745	65829746	G	A	17	GENIC	homozygous	51478400
10	65829803	65829804	G	GCCTAGCAAGCGCAAGGC	21	GENIC	homozygous	51478401
10	65830492	65830493	G	C	37	GENIC	homozygous	51478402
10	65831157	65831158	T	C	17	GENIC	homozygous	51478403
10	65831257	65831258	C	T	25	GENIC	homozygous	51907217
10	65831708	65831709	T	C	34	GENIC	homozygous	51478404
10	65832036	65832037	T	G	27	GENIC	homozygous	51478405
10	65832071	65832072	G	-	16	GENIC	homozygous	51478406