chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	32973755	32973756	T	G	66	GENIC	homozygous	111031304
17	32974704	32974705	T	A	33	GENIC	possibly homozygous	111402385
17	32975027	32975028	C	G	59	GENIC	homozygous	111031306
17	32976432	32976433	C	T	57	GENIC	possibly homozygous	111031308
17	32976889	32976890	G	A	64	GENIC	homozygous	111031310
17	32977212	32977213	C	T	41	GENIC	homozygous	111031313
17	32977960	32977961	A	G	69	GENIC	homozygous	111031315
17	32979555	32979556	T	C	50	GENIC	homozygous	111031317
17	32979678	32979679	G	A	65	GENIC	homozygous	111031319
17	32980350	32980351	G	A	68	GENIC	possibly homozygous	111031321
17	32981109	32981110	T	C	51	GENIC	possibly homozygous	111031323
17	32984088	32984089	C	A	64	GENIC	homozygous	111031325
17	32985975	32985976	C	T	68	GENIC	homozygous	111031327
17	32986828	32986829	C	A	32	GENIC	possibly homozygous	119280630
17	32986835	32986836	G	C	32	GENIC	heterozygous	119280632
17	32987193	32987194	T	A	46	GENIC	homozygous	111031329
17	32987473	32987474	G	A	43	GENIC	homozygous	111031333
17	32987681	32987682	T	A	87	GENIC	homozygous	111031335
17	32987948	32987949	C	T	78	GENIC	homozygous	111031337
17	32987956	32987957	A	G	78	GENIC	possibly homozygous	111031339
17	32988123	32988124	G	A	50	GENIC	homozygous	111031341
17	32988498	32988499	G	C	34	GENIC	homozygous	111192340
17	32989601	32989602	C	T	64	GENIC	homozygous	111031343
17	32989981	32989982	G	A	69	GENIC	homozygous	111031345
17	32989984	32989985	C	T	70	GENIC	homozygous	111031347