chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	84418668	84418669	G	T	18	GENIC	homozygous	118464585
13	84418672	84418673	G	C	17	GENIC	homozygous	118464586
13	84418674	84418674		GCT	17	GENIC	homozygous	129081279
13	84418676	84418679	GGG		18	GENIC	homozygous	129081280
13	84418681	84418682	G	A	18	GENIC	homozygous	118464587
13	84418704	84418705	A	G	17	GENIC	homozygous	123776721
13	84418834	84418835	G	T	25	GENIC	homozygous	114417987
13	84418835	84418836	G	T	25	GENIC	homozygous	114417989
13	84428170	84428171	A		11	GENIC	homozygous	129081288
13	84428186	84428186		G	11	GENIC	homozygous	129081289
13	84428190	84428191	A		12	GENIC	homozygous	129081290
13	84428195	84428196	G		12	GENIC	homozygous	129081291
13	84428205	84428206	A	G	11	GENIC	homozygous	114417999
13	84428336	84428339	CAT		16	GENIC	heterozygous	129081293
13	84437564	84437564		A	27	GENIC	heterozygous	129081295
13	84437594	84437595	G	A	29	GENIC	heterozygous	118502444
13	84437609	84437610	T	A	28	GENIC	heterozygous	118502445
13	84437613	84437614	T	G	28	GENIC	heterozygous	123776738
13	84437616	84437617	A	G	28	GENIC	heterozygous	123776739
13	84437636	84437637	A	G	27	GENIC	heterozygous	118502446
13	84437659	84437660	C	T	23	GENIC	heterozygous	123833876