chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	39121937	39121938	T	A	27	GENIC	homozygous	111305431
17	39127408	39127409	A	G	39	GENIC	homozygous	111042276
17	39128272	39128273	T	C	50	GENIC	homozygous	111042288
17	39129182	39129183	C	G	35	GENIC	homozygous	111305432
17	39129508	39129509	C	A	45	GENIC	homozygous	111042296
17	39130156	39130157	C	T	34	GENIC	homozygous	111305434
17	39130220	39130221	C	T	33	GENIC	homozygous	111201202
17	39130654	39130655	T	C	57	GENIC	homozygous	111201203
17	39130789	39130790	T	G	49	GENIC	homozygous	111305435
17	39130988	39130989	C	T	38	GENIC	homozygous	111042304
17	39131098	39131099	A	G	34	GENIC	homozygous	111305436
17	39131727	39131728	A	G	42	GENIC	homozygous	111305437
17	39131739	39131740	T	C	44	GENIC	homozygous	111305438
17	39131765	39131766	T	C	46	GENIC	homozygous	111305439
17	39131821	39131822	C	T	48	GENIC	homozygous	111305440
17	39131947	39131948	T	C	48	GENIC	homozygous	111042308
17	39131958	39131959	A	G	47	GENIC	homozygous	111042310