chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	85602110	85602111	T	C	19	GENIC	homozygous	118464993
13	85602294	85602295	G	A	32	GENIC	homozygous	118464994
13	85602297	85602298	C	A	32	GENIC	homozygous	114422428
13	85602710	85602711	T	C	18	GENIC	heterozygous	114645908
13	85603177	85603178	T	C	57	GENIC	homozygous	114422430
13	85603804	85603805	A	T	56	GENIC	homozygous	114422432
13	85604639	85604640	T	C	35	GENIC	homozygous	114422434
13	85605396	85605397	A	G	73	GENIC	homozygous	114422436
13	85606248	85606249	T	C	48	GENIC	homozygous	114422438
13	85607227	85607228	C	T	44	GENIC	homozygous	114422440
13	85607771	85607772	G	C	31	GENIC	homozygous	114422442
13	85607856	85607857	C	A	39	GENIC	possibly homozygous	114422444
13	85609613	85609614	G	A	50	GENIC	homozygous	114422446
13	85610084	85610085	T	A	34	GENIC	homozygous	114422452
13	85610101	85610102	C	G	36	GENIC	homozygous	114422454
13	85610126	85610127	C	T	40	GENIC	homozygous	114422456
13	85610135	85610136	C	A	44	GENIC	possibly homozygous	114422458
13	85611089	85611090	G	A	50	GENIC	homozygous	114422460
13	85612221	85612222	T	C	38	GENIC	possibly homozygous	114422462
13	85613359	85613360	T	G	50	GENIC	homozygous	114422464
13	85613588	85613589	C	G	49	GENIC	homozygous	114422466
13	85614773	85614774	C	T	57	GENIC	homozygous	114422468
13	85614844	85614845	G	T	49	GENIC	possibly homozygous	118464995
13	85615133	85615134	G	A	37	GENIC	homozygous	114422470
13	85615536	85615537	C	G	20	GENIC	possibly homozygous	114830687
13	85615687	85615688	A	G	51	GENIC	homozygous	114422472
13	85615722	85615723	A	G	50	GENIC	homozygous	114422474
13	85618231	85618232	C	T	63	GENIC	homozygous	114422476
13	85621742	85621743	C	A	26	GENIC	homozygous	118464996