chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	9238583	9238584	A	G	43	GENIC	homozygous	111443029
3	9238698	9238699	C	T	38	GENIC	homozygous	111443030
3	9241067	9241068	A	G	40	GENIC	heterozygous	111443031
3	9241282	9241283	G	A	30	GENIC	heterozygous	111443032
3	9242247	9242248	G	A	22	GENIC	homozygous	111443033
3	9242289	9242290	A	G	21	GENIC	homozygous	111443034
3	9243556	9243557	G	A	34	GENIC	possibly homozygous	111443035
3	9243870	9243871	G	A	39	GENIC	possibly homozygous	111443036
3	9246004	9246005	C	T	28	GENIC	homozygous	111443037
3	9246672	9246673	A	G	34	GENIC	homozygous	111443038
3	9247511	9247512	T	C	23	GENIC	homozygous	111443039
3	9248391	9248392	C	A	15	GENIC	heterozygous	111443040
3	9248403	9248404	C	A	13	GENIC	heterozygous	111443042
3	9248739	9248740	T	G	34	GENIC	heterozygous	111443043
3	9248999	9249000	T	G	21	GENIC	heterozygous	111443044
3	9255095	9255096	T	C	33	GENIC	homozygous	111443046
3	9256906	9256907	C	T	45	GENIC	possibly homozygous	111443047
3	9256927	9256928	C	T	45	GENIC	homozygous	111443048
3	9256929	9256930	A	G	45	GENIC	possibly homozygous	111443049
3	9257324	9257325	C	A	28	GENIC	homozygous	111443050
3	9257339	9257340	C	A	33	GENIC	homozygous	111873368
3	9257584	9257585	T	G	34	GENIC	homozygous	111443051
3	9258046	9258047	C	G	42	GENIC	possibly homozygous	111443052
3	9258211	9258212	T	C	39	GENIC	homozygous	111443053
3	9258248	9258249	A	C	42	GENIC	homozygous	111443054
3	9258562	9258563	G	T	30	GENIC	homozygous	111443055
3	9258625	9258626	G	A	25	GENIC	homozygous	111443056
3	9258638	9258639	A	G	32	GENIC	homozygous	111443057
3	9258680	9258681	T	C	37	GENIC	homozygous	111443058
3	9259100	9259101	G	A	21	GENIC	homozygous	111443059
3	9259938	9259939	A	G	35	GENIC	homozygous	111443060
3	9260204	9260205	A	G	31	GENIC	homozygous	111443061
3	9260253	9260254	C	T	32	GENIC	homozygous	111443062
3	9260301	9260302	A	G	32	GENIC	homozygous	111443063
3	9260699	9260700	A	G	28	GENIC	homozygous	111443064
3	9261479	9261480	C	G	18	GENIC	homozygous	111443065