chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	23005871	23005872	A	G	13	GENIC	homozygous	61273480
1	23006481	23006482	A	G	27	GENIC	possibly homozygous	61273481
1	23006639	23006640	A	C	8	GENIC	heterozygous	62526746
1	23006640	23006641	G	T	8	GENIC	heterozygous	62526747
1	23009479	23009481	TT	--	3	GENIC	heterozygous	61273485
1	23009914	23009915	T	C	28	GENIC	possibly homozygous	62611921
1	23009915	23009916	G	A	27	GENIC	possibly homozygous	62611922
1	23009948	23009949	C	T	15	GENIC	homozygous	62611923
1	23009951	23009952	G	A	16	GENIC	homozygous	62526749
1	23010103	23010104	G	A	18	GENIC	heterozygous	61273487
1	23010179	23010182	TTT	---	2	GENIC	heterozygous	62611924
1	23010467	23010468	G	T	17	GENIC	homozygous	61395140
1	23010817	23010818	A	G	17	GENIC	homozygous	62526750
1	23011069	23011070	A	G	18	GENIC	homozygous	61273489
1	23011166	23011167	G	A	13	GENIC	homozygous	62611925
1	23011223	23011224	T	G	18	GENIC	possibly homozygous	61273490
1	23011254	23011255	G	C	7	GENIC	heterozygous	61273491
1	23011303	23011304	A	G	6	GENIC	heterozygous	61273492
1	23011762	23011763	T	C	9	GENIC	homozygous	61273495
1	23011781	23011782	C	G	3	GENIC	homozygous	61273496
1	23011785	23011786	G	A	2	GENIC	homozygous	61273497
1	23012020	23012021	T	C	13	GENIC	homozygous	61273498
1	23012978	23012979	T	C	1	GENIC	homozygous	61395151
1	23013067	23013068	T	-	3	GENIC	heterozygous	61273503
1	23013498	23013499	T	C	16	GENIC	homozygous	61273504
1	23013756	23013757	G	A	8	GENIC	heterozygous	62611926
1	23014048	23014050	TG	--	3	GENIC	heterozygous	62480431
1	23014157	23014158	A	G	12	GENIC	homozygous	61273508
1	23014199	23014200	A	G	11	GENIC	homozygous	61273509
1	23014681	23014682	T	C	13	GENIC	homozygous	61273511
1	23015216	23015218	AT	--	22	GENIC	homozygous	61273512
1	23015237	23015238	A	G	20	GENIC	possibly homozygous	61273513
1	23016197	23016198	G	GTATA	1	GENIC	homozygous	62611927
1	23016359	23016360	G	A	14	GENIC	homozygous	61981265