chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	85676247	85676248	C	G	32	GENIC	homozygous	114422566
13	85676377	85676378	G	T	33	GENIC	homozygous	114422568
13	85676500	85676501	C	T	33	GENIC	homozygous	114422570
13	85676561	85676562	C	T	47	GENIC	homozygous	114422572
13	85677037	85677038	C	T	9	GENIC	homozygous	114422574
13	85677406	85677407	C	A	53	GENIC	homozygous	114422576
13	85677840	85677841	A	T	32	GENIC	homozygous	114422578
13	85678628	85678629	G	A	45	GENIC	homozygous	114422580
13	85678705	85678706	C	T	44	GENIC	homozygous	114422582
13	85678954	85678955	T	C	37	GENIC	homozygous	114422584
13	85680508	85680509	A	T	41	GENIC	homozygous	114422586
13	85681076	85681077	G	A	37	GENIC	homozygous	114422588
13	85681329	85681330	G	C	32	GENIC	homozygous	114422590
13	85681645	85681646	G	A	36	GENIC	homozygous	114422592
13	85683956	85683957	T	C	58	GENIC	homozygous	114422594
13	85686714	85686715	C	T	46	GENIC	homozygous	114422596
13	85687789	85687790	T	G	67	GENIC	homozygous	114422598
13	85688264	85688265	G	A	25	GENIC	homozygous	114422600
13	85689328	85689329	A	G	29	GENIC	homozygous	114422602
13	85689805	85689806	C	T	50	GENIC	homozygous	114422604
13	85691695	85691696	G	A	20	GENIC	homozygous	114422606
13	85692161	85692162	G	A	43	GENIC	homozygous	114422608
13	85693485	85693486	T	C	31	GENIC	homozygous	114422610
13	85694226	85694227	G	T	28	GENIC	homozygous	114422612
13	85694396	85694397	C	T	42	GENIC	homozygous	114422614