chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	52707866	52707867	C	T	26	GENIC	homozygous	50230440
13	52708496	52708498	AA	--	18	GENIC	homozygous	49948652
13	52708547	52708548	T	C	23	GENIC	homozygous	50040672
13	52708865	52708866	C	T	28	GENIC	homozygous	50040674
13	52709642	52709643	A	G	27	GENIC	homozygous	49948659
13	52709921	52709922	A	G	24	GENIC	homozygous	49948660
13	52710180	52710181	G	A	27	GENIC	homozygous	50361177
13	52710686	52710687	G	A	28	GENIC	homozygous	49948661
13	52710721	52710723	CA	--	3	GENIC	heterozygous	50563180
13	52710871	52710872	G	A	32	GENIC	homozygous	49948662
13	52711025	52711026	G	C	22	GENIC	homozygous	49948663
13	52711230	52711231	G	A	26	GENIC	homozygous	49948664
13	52711250	52711251	C	T	24	GENIC	homozygous	49948665
13	52711341	52711342	C	T	22	GENIC	homozygous	49948666
13	52711355	52711356	T	C	24	GENIC	homozygous	49948667
13	52711380	52711381	T	C	26	GENIC	homozygous	49948669
13	52711633	52711634	C	A	22	GENIC	homozygous	49948670
13	52711791	52711792	G	A	26	GENIC	homozygous	49948671
13	52711802	52711803	A	G	27	GENIC	homozygous	49948672
13	52711821	52711822	A	G	20	GENIC	homozygous	49948673
13	52711857	52711858	G	A	16	GENIC	homozygous	49948674
13	52712149	52712150	T	C	24	GENIC	homozygous	49948676
13	52712269	52712270	C	T	23	GENIC	homozygous	49948677
13	52712362	52712363	T	C	17	GENIC	homozygous	49948678
13	52712429	52712430	G	A	35	GENIC	homozygous	49948680