chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	200306428	200306429	A	G	31	GENIC	homozygous	59926459
2	200306462	200306463	G	A	36	GENIC	homozygous	59926460
2	200307424	200307425	G	A	31	GENIC	homozygous	59926462
2	200307602	200307603	A	G	14	GENIC	homozygous	59926463
2	200307795	200307796	T	TA	29	GENIC	homozygous	59337440
2	200307921	200307922	T	C	29	GENIC	homozygous	59926464
2	200308045	200308046	C	T	28	GENIC	homozygous	59926465
2	200309622	200309623	T	C	41	GENIC	homozygous	59926466
2	200310785	200310786	A	G	12	GENIC	homozygous	59926467
2	200311482	200311483	C	CTAA	37	GENIC	homozygous	59926468
2	200311529	200311530	A	T	29	GENIC	homozygous	59926469
2	200311878	200311879	A	-	28	GENIC	homozygous	59926470
2	200314978	200314979	A	-	29	GENIC	homozygous	59926471
2	200315006	200315007	A	C	33	GENIC	homozygous	59337445
2	200315528	200315529	T	C	25	GENIC	homozygous	59337446
2	200316096	200316097	T	A	37	GENIC	homozygous	59926473
2	200316433	200316434	T	A	22	GENIC	homozygous	59926474
2	200316488	200316489	G	A	22	GENIC	homozygous	59926475
2	200316508	200316509	A	AT	20	GENIC	homozygous	59926476
2	200318455	200318456	T	TC	4	GENIC	heterozygous	59337447
2	200319078	200319079	A	C	18	GENIC	homozygous	59337450
2	200319856	200319857	T	C	32	GENIC	homozygous	59337451
2	200320201	200320202	C	G	28	GENIC	homozygous	59926478
2	200320205	200320206	G	A	29	GENIC	homozygous	59926479