chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	65416009	65416010	C	A	26	GENIC	homozygous	51477692
10	65416051	65416052	G	A	24	GENIC	homozygous	51906324
10	65416156	65416157	G	A	17	GENIC	homozygous	51906326
10	65416178	65416179	C	A	12	GENIC	homozygous	51477694
10	65416186	65416187	A	G	11	GENIC	homozygous	51477695
10	65416210	65416211	T	C	9	GENIC	homozygous	51477696
10	65416370	65416371	G	A	8	GENIC	homozygous	51906328
10	65416487	65416488	G	T	1	GENIC	homozygous	51477700
10	65416489	65416490	T	C	2	GENIC	homozygous	51477701
10	65416608	65416609	G	A	6	GENIC	homozygous	51477703
10	65416649	65416650	G	GTTA	1	GENIC	homozygous	51906333
10	65416651	65416652	G	GAGGGC	1	GENIC	homozygous	51906335
10	65416816	65416817	A	C	1	GENIC	homozygous	51906337
10	65416839	65416843	TTTG	----	10	GENIC	homozygous	51906339
10	65416869	65416870	G	T	9	GENIC	homozygous	51906341
10	65416963	65416964	G	A	4	GENIC	homozygous	51477708
10	65416969	65416970	A	T	1	GENIC	homozygous	51477709
10	65416289	65416291	TG	--	10	GENIC	possibly homozygous	52320241
10	65416290	65416291	G	GCCA	10	GENIC	possibly homozygous	52320243
10	65417632	65417633	G	GT	2	GENIC	heterozygous	51477714
10	65417763	65417764	C	G	10	GENIC	possibly homozygous	51477717
10	65417764	65417765	T	C	10	GENIC	possibly homozygous	51477718
10	65417919	65417920	A	G	8	GENIC	homozygous	51477721
10	65418476	65418477	G	T	15	GENIC	homozygous	51906345
10	65418608	65418609	A	G	7	GENIC	homozygous	51477728
10	65418754	65418755	C	A	12	GENIC	homozygous	51906347
10	65418763	65418764	A	C	10	GENIC	homozygous	51477730
10	65418816	65418817	G	A	5	GENIC	heterozygous	51906349
10	65418823	65418824	A	G	5	GENIC	homozygous	51477731