chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	69308524	69308525	T	C	14	GENIC	homozygous	51686938
10	69308898	69308899	A	G	21	GENIC	homozygous	51686940
10	69309700	69309701	T	C	14	GENIC	homozygous	51686942
10	69310057	69310058	T	C	13	GENIC	homozygous	51686944
10	69310246	69310247	G	A	22	GENIC	homozygous	51686946
10	69310276	69310277	T	C	15	GENIC	homozygous	51686948
10	69310657	69310658	C	CT	17	GENIC	heterozygous	53528910
10	69310906	69310907	G	C	12	GENIC	homozygous	51686950
10	69311049	69311050	C	CAAAAAAAGA	14	GENIC	homozygous	51686952
10	69311433	69311434	C	A	20	GENIC	homozygous	51686956
10	69311642	69311643	A	G	17	GENIC	homozygous	51686958
10	69311719	69311720	C	T	11	GENIC	homozygous	51686960
10	69311805	69311806	C	G	27	GENIC	homozygous	51686962
10	69312226	69312228	TG	--	11	GENIC	homozygous	51485028
10	69312790	69312791	C	A	19	GENIC	homozygous	51686964
10	69313228	69313229	A	C	25	GENIC	homozygous	51686966
10	69314478	69314479	A	G	17	GENIC	homozygous	51686968
10	69314479	69314480	T	TG	17	GENIC	homozygous	51686970
10	69314667	69314668	T	C	13	GENIC	homozygous	51686972
10	69315160	69315161	C	T	17	GENIC	homozygous	51686976
10	69315458	69315462	TGTT	----	7	GENIC	homozygous	51485030
10	69315805	69315806	C	T	15	GENIC	homozygous	51686978
10	69316288	69316289	G	A	12	GENIC	homozygous	51686982