chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	61434153	61434154	T	G	22	GENIC	possibly homozygous	117061484
10	61434168	61434169	C	T	26	GENIC	homozygous	117061486
10	61434565	61434566	A	G	28	GENIC	homozygous	117061488
10	61434782	61434783	C	T	14	GENIC	homozygous	117061490
10	61438293	61438294	A	C	14	GENIC	homozygous	116790547
10	61438323	61438324	A	G	14	GENIC	homozygous	117061492
10	61438618	61438619	G	A	38	GENIC	homozygous	117061494
10	61440699	61440700	T	C	27	GENIC	homozygous	116612797
10	61442897	61442898	C	T	25	GENIC	homozygous	117061496
10	61445490	61445491	G	T	21	GENIC	homozygous	116790551
10	61446223	61446224	T	A	23	GENIC	homozygous	117061498
10	61446484	61446485	G	A	16	GENIC	homozygous	116790553
10	61446491	61446492	T	C	17	GENIC	homozygous	117061500
10	61448937	61448938	T	C	18	GENIC	possibly homozygous	117061502
10	61450778	61450779	G	A	34	GENIC	homozygous	116612805