chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	102136370	102136371	C	T	25	GENIC	homozygous	116712598
10	102136379	102136380	C	G	24	GENIC	homozygous	116712600
10	102136618	102136618		G	22	GENIC	homozygous	128854473
10	102136651	102136652	G	A	19	GENIC	homozygous	116712602
10	102136666	102136667	T	C	17	GENIC	homozygous	116712604
10	102138186	102138187	C	G	11	GENIC	possibly homozygous	116712606
10	102138273	102138274	C	T	10	GENIC	possibly homozygous	116712608
10	102138431	102138432	C	A	28	GENIC	homozygous	116712610
10	102138625	102138626	C	G	16	GENIC	homozygous	116712612
10	102138627	102138628	G	A	16	GENIC	homozygous	116712614
10	102138634	102138635	G	C	14	GENIC	homozygous	116712616
10	102138638	102138639	G	A	14	GENIC	homozygous	116712618
10	102138849	102138850	G	A	26	GENIC	homozygous	116712620
10	102138955	102138959	CGCG		22	GENIC	homozygous	128854474
10	102138973	102138974	C	T	22	GENIC	homozygous	116712622
10	102139395	102139396	A		14	GENIC	homozygous	128854475
10	102139399	102139400	G	A	14	GENIC	homozygous	116712624
10	102140833	102140834	T	C	19	GENIC	homozygous	116712626
10	102140843	102140844	A	C	19	GENIC	homozygous	116712628
10	102140976	102140988	ACACACACACAT		14	GENIC	homozygous	128854476
10	102141381	102141382	C	T	16	GENIC	homozygous	118011885
10	102141392	102141393	G	A	15	GENIC	homozygous	118011886
10	102140973	102140974	T	G	14	GENIC	homozygous	117232363