chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	2462064	2462065	T	C	37	GENIC	homozygous	115357439
12	2462335	2462336	C	A	46	GENIC	homozygous	115234455
12	2463546	2463547	T	C	33	GENIC	homozygous	115234457
12	2464647	2464648	G	C	48	GENIC	homozygous	115234461
12	2465830	2465831	T	G	44	GENIC	homozygous	115234467
12	2466579	2466580	T	G	40	GENIC	homozygous	115234469
12	2466902	2466903	T	G	39	GENIC	homozygous	115234471
12	2468457	2468458	G	C	53	GENIC	homozygous	115234473
12	2469141	2469142	A	G	35	GENIC	possibly homozygous	115357440
12	2470823	2470824	G	A	46	GENIC	homozygous	115234479
12	2473496	2473497	T	C	33	GENIC	homozygous	115234483
12	2473582	2473583	G	A	49	GENIC	homozygous	115357441
12	2473646	2473647	G	A	56	GENIC	homozygous	115234485
12	2475668	2475669	G	T	33	GENIC	possibly homozygous	115357442
12	2476132	2476133	C	T	37	GENIC	homozygous	115357443
12	2476879	2476880	T	G	30	GENIC	homozygous	115357444
12	2477569	2477570	T	C	37	GENIC	homozygous	115234493
12	2479072	2479073	A	G	45	GENIC	homozygous	115234495
12	2479226	2479227	G	A	35	GENIC	homozygous	115234497
12	2481895	2481896	G	A	39	GENIC	possibly homozygous	115357445
12	2482331	2482332	T	C	43	GENIC	homozygous	115234507
12	2488931	2488932	A	C	26	GENIC	homozygous	115234525
12	2473830	2473831	T	C	34	GENIC	possibly homozygous	118235204