chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	46071362	46071363	C	G	12	GENIC	homozygous	119290603
17	46073059	46073060	T	A	46	GENIC	homozygous	111055163
17	46073096	46073097	C	T	52	GENIC	homozygous	111055165
17	46073105	46073106	C	T	50	GENIC	homozygous	111055167
17	46073140	46073141	G	A	52	GENIC	homozygous	111055169
17	46073317	46073318	G	A	32	GENIC	homozygous	111055171
17	46073451	46073452	C	A	37	GENIC	heterozygous	119290604
17	46073453	46073454	A	G	38	GENIC	heterozygous	119290605
17	46074425	46074426	T	C	18	GENIC	homozygous	111055175
17	46076816	46076817	G	T	54	GENIC	homozygous	111055177
17	46077058	46077059	A	G	20	GENIC	homozygous	111055179
17	46078558	46078559	C	T	28	GENIC	homozygous	111055181
17	46079460	46079461	T	G	18	GENIC	possibly homozygous	119290606
17	46079476	46079477	C	G	23	GENIC	heterozygous	119290607
17	46080293	46080294	A	G	33	GENIC	homozygous	111055183
17	46080422	46080423	G	A	20	GENIC	homozygous	111055185
17	46081264	46081265	A	T	47	GENIC	homozygous	111055187