chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	66008535	66008536	T	C	34	GENIC	homozygous	51907672
10	66009428	66009429	A	G	43	GENIC	homozygous	51478966
10	66010218	66010219	C	CAA	9	GENIC	heterozygous	51478970
10	66010223	66010225	AC	--	16	GENIC	heterozygous	51478971
10	66011074	66011075	A	AG	26	GENIC	homozygous	51478972
10	66014304	66014307	GGG	---	4	GENIC	heterozygous	51907674
10	66014305	66014307	GG	--	4	GENIC	heterozygous	51907676
10	66014316	66014318	GT	--	13	GENIC	heterozygous	51907678
10	66014431	66014432	A	AACACAC	7	GENIC	heterozygous	51478975
10	66014431	66014432	A	AACAC	7	GENIC	heterozygous	51987832
10	66015886	66015887	A	C	27	GENIC	homozygous	51907680
10	66017573	66017577	AAAC	----	21	GENIC	homozygous	51478978
10	66017828	66017829	G	A	30	GENIC	possibly homozygous	51907682
10	66018920	66018922	CA	--	5	GENIC	homozygous	51478979
10	66019303	66019304	C	T	25	GENIC	heterozygous	51478980
10	66019307	66019308	C	T	26	GENIC	heterozygous	51478981
10	66022206	66022208	TG	--	16	GENIC	homozygous	51907684
10	66022761	66022765	GCCT	----	4	GENIC	homozygous	51478987
10	66022801	66022802	G	T	8	GENIC	heterozygous	52063024
10	66022832	66022833	C	CCTT	2	GENIC	homozygous	51478989
10	66022959	66022960	C	CAAA	4	GENIC	homozygous	51907686
10	66024775	66024776	G	C	14	GENIC	possibly homozygous	51907690
10	66024777	66024778	G	C	11	GENIC	heterozygous	51907692
10	66024918	66024920	AA	--	6	GENIC	heterozygous	51478997
10	66024919	66024920	A	-	6	GENIC	heterozygous	51478998
10	66026787	66026788	C	T	27	GENIC	homozygous	51907694
10	66026825	66026826	C	A	24	GENIC	homozygous	51907696
10	66027701	66027702	T	C	37	GENIC	homozygous	51479001
10	66030131	66030132	C	G	27	GENIC	homozygous	51907698