chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	55475476	55475477	A	C	58	GENIC	homozygous	143887875
3	55476628	55476629	G	A	59	GENIC	homozygous	136709530
3	55477051	55477052	A	G	51	GENIC	homozygous	136709531
3	55477320	55477321	C	T	63	GENIC	homozygous	136709532
3	55477925	55477926	G	A	70	GENIC	homozygous	145410609
3	55479051	55479052	A		39	GENIC	homozygous	136563606
3	55479077	55479078	C	T	45	GENIC	homozygous	145410610
3	55480292	55480293	G	A	47	GENIC	homozygous	136709534
3	55480962	55480963	C	A	53	GENIC	homozygous	136709535
3	55483574	55483575	C	T	62	GENIC	homozygous	136709537
3	55483864	55483864		TGTT	52	GENIC	homozygous	136563609
3	55484488	55484489	C	T	55	GENIC	homozygous	143887877
3	55485238	55485239	G	A	69	GENIC	homozygous	136709538
3	55481415	55481416	A		49	GENIC	possibly homozygous	403064532
3	55486518	55486519	C	T	62	GENIC	homozygous	143887879
3	55487128	55487129	G	A	56	GENIC	homozygous	136709540
3	55488043	55488044	G	A	37	GENIC	homozygous	143887880
3	55488810	55488811	T	C	43	GENIC	homozygous	143887881
3	55481415	55481416	A	G	49	GENIC	heterozygous	403064533
3	55484320	55484321	T	C	21	GENIC	possibly homozygous	403064534
3	55489455	55489456	A	T	33	GENIC	homozygous	136709541
3	55490188	55490189	G	A	53	GENIC	homozygous	154095530
3	55490448	55490449	A	G	52	GENIC	homozygous	136709542
3	55491995	55491996	A	G	59	GENIC	homozygous	143887882
3	55492079	55492080	G	C	59	GENIC	homozygous	143887883
3	55492562	55492563	A	T	50	GENIC	homozygous	136709544
3	55492581	55492582	T	G	53	GENIC	homozygous	143887884
3	55492684	55492685	G	A	51	GENIC	homozygous	145410611
3	55494659	55494668	CTTACAGTG		42	GENIC	homozygous	143856404
3	55497440	55497442	CT		62	GENIC	homozygous	143856405
3	55498700	55498701	C	A	49	GENIC	homozygous	143887886
3	55502192	55502192		CTGACAAGAGGCAGCTGTAA	56	GENIC	homozygous	136563612
3	55490188	55490189	G		53	GENIC	heterozygous	403711843
3	55500615	55500616	T	C	43	GENIC	homozygous	136709548
3	55502276	55502277	C	T	68	GENIC	homozygous	143887887