chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	82593241	82593242	C	T	27	GENIC	possibly homozygous	114411433
13	82593742	82593743	T	A	20	GENIC	homozygous	114411435
13	82594804	82594805	T	C	17	GENIC	homozygous	114411437
13	82595117	82595118	T	C	15	GENIC	possibly homozygous	114411439
13	82595557	82595558	A	G	17	GENIC	homozygous	114411441
13	82595631	82595632	C	T	16	GENIC	homozygous	114411443
13	82595951	82595952	C	T	21	GENIC	homozygous	114411445
13	82596831	82596832	T	G	14	GENIC	homozygous	114411447
13	82597499	82597500	C	T	15	GENIC	homozygous	114411449
13	82597646	82597647	T	C	25	GENIC	homozygous	114411451
13	82597674	82597675	T	C	19	GENIC	homozygous	114411453
13	82597699	82597700	C	T	21	GENIC	homozygous	114411455
13	82598162	82598163	T	A	22	GENIC	homozygous	114411457
13	82598558	82598559	T	A	33	GENIC	homozygous	114411459
13	82598901	82598902	C	A	21	GENIC	homozygous	114411461
13	82598983	82598984	T	C	12	GENIC	homozygous	114411463
13	82599175	82599176	A	G	22	GENIC	homozygous	114411465
13	82599672	82599673	C	T	17	GENIC	homozygous	114411467
13	82600001	82600002	T	G	11	GENIC	homozygous	114411469
13	82600444	82600445	A	G	28	GENIC	homozygous	114411471
13	82601747	82601748	T	C	19	GENIC	homozygous	114411473
13	82602712	82602713	C	T	19	GENIC	homozygous	114411475
13	82603037	82603038	T	C	20	GENIC	homozygous	114411481
13	82603056	82603057	G	A	16	GENIC	homozygous	114411483
13	82596586	82596587	G	A	28	GENIC	possibly homozygous	114567192
13	82603361	82603362	C	G	11	GENIC	homozygous	114411485
13	82603476	82603477	T	C	19	GENIC	homozygous	114411487
13	82604011	82604012	G	A	19	GENIC	homozygous	114411489
13	82603360	82603361	C	G	11	GENIC	homozygous	114830476
13	82603350	82603351	T	C	12	GENIC	heterozygous	118582758
13	82603370	82603371	C	T	20	GENIC	homozygous	114987174
13	82605678	82605679	C	T	14	GENIC	homozygous	114411491
13	82607126	82607127	T	C	33	GENIC	homozygous	114411493