chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	85603177	85603178	T	C	39	GENIC	homozygous	114422430
13	85603804	85603805	A	T	47	GENIC	homozygous	114422432
13	85605396	85605397	A	G	43	GENIC	homozygous	114422436
13	85606248	85606249	T	C	60	GENIC	homozygous	114422438
13	85607227	85607228	C	T	32	GENIC	homozygous	114422440
13	85607856	85607857	C	A	13	GENIC	possibly homozygous	114422444
13	85609613	85609614	G	A	54	GENIC	homozygous	114422446
13	85610084	85610085	T	A	41	GENIC	homozygous	114422452
13	85610101	85610102	C	G	47	GENIC	homozygous	114422454
13	85611089	85611090	G	A	60	GENIC	homozygous	114422460
13	85613359	85613360	T	G	38	GENIC	homozygous	114422464
13	85613588	85613589	C	G	31	GENIC	homozygous	114422466
13	85614773	85614774	C	T	87	GENIC	homozygous	114422468
13	85615133	85615134	G	A	32	GENIC	homozygous	114422470
13	85615687	85615688	A	G	53	GENIC	homozygous	114422472
13	85615722	85615723	A	G	49	GENIC	homozygous	114422474
13	85618231	85618232	C	T	41	GENIC	homozygous	114422476