chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	153802484	153802485	T	C	57	GENIC	homozygous	110063043
2	153826008	153826009	A	G	33	GENIC	homozygous	110063120
2	153826596	153826596		C	9	GENIC	homozygous	127692563
2	153832698	153832699	C	G	40	GENIC	homozygous	120150909
2	153826389	153826390	A	G	4	GENIC	homozygous	127807944
2	153832694	153832695	C	T	37	GENIC	homozygous	110063142
2	153832696	153832697	C	A	39	GENIC	homozygous	120150908
2	153832767	153832768	C	G	37	GENIC	homozygous	110063143
2	153832771	153832772	C	G	39	GENIC	homozygous	110598431
2	153832773	153832774	C	G	38	GENIC	homozygous	110976488
2	153832775	153832776	A	G	38	GENIC	homozygous	110976490
2	153849402	153849403	G		58	GENIC	homozygous	127692571
2	153849536	153849537	A		64	GENIC	homozygous	127692572
2	153856366	153856366		A	32	GENIC	homozygous	127692577
2	153862239	153862239		T	51	GENIC	homozygous	127692581
2	153862241	153862242	G		53	GENIC	homozygous	127692582
2	153862252	153862253	A	C	51	GENIC	homozygous	121499146
2	153862253	153862254	C	T	51	GENIC	homozygous	110063239
2	153864182	153864182		C	13	GENIC	homozygous	127692584
2	153864446	153864447	T	G	19	GENIC	homozygous	110063245
2	153877338	153877338		CAGG	56	GENIC	homozygous	127692587
2	153836906	153836907	C	G	58	GENIC	possibly homozygous	111331261
2	153839480	153839480		CTTT	18	GENIC	heterozygous	132945321