chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	98345554	98345555	C	A	33	GENIC	homozygous	52067364
9	98346896	98346897	A	G	24	GENIC	homozygous	52067367
9	98348255	98348256	G	GT	10	GENIC	heterozygous	52067385
9	98348255	98348256	G	GTT	10	GENIC	possibly homozygous	52067388
9	98348358	98348359	G	GA	14	GENIC	possibly homozygous	52067391
9	98349815	98349816	T	A	27	GENIC	homozygous	52067393
9	98349935	98349936	A	G	30	GENIC	homozygous	52067396
9	98349948	98349949	T	C	27	GENIC	homozygous	52067399
9	98350078	98350079	A	T	13	GENIC	homozygous	52443011
9	98350315	98350316	G	T	20	GENIC	homozygous	52067402
9	98352058	98352060	TT	--	20	GENIC	homozygous	52443013
9	98352070	98352071	T	G	22	GENIC	homozygous	53312712
9	98353656	98353657	C	G	22	GENIC	homozygous	52443015
9	98354407	98354408	T	C	22	GENIC	homozygous	52067420
9	98354688	98354689	C	T	32	GENIC	homozygous	52443017
9	98355064	98355065	G	C	35	GENIC	homozygous	52443019
9	98355727	98355728	T	C	20	GENIC	homozygous	52067423
9	98356050	98356051	C	T	22	GENIC	homozygous	52443021
9	98356665	98356666	T	C	20	GENIC	homozygous	52443023
9	98358118	98358124	AGAGAG	------	12	GENIC	homozygous	52443025
9	98358167	98358168	A	AG	21	GENIC	homozygous	52443027
9	98358169	98358170	A	AGG	21	GENIC	homozygous	52443029
9	98360042	98360043	C	T	21	GENIC	homozygous	52443031
9	98362546	98362548	TT	--	10	GENIC	homozygous	52443033
9	98363399	98363400	T	C	20	GENIC	homozygous	52067464
9	98363447	98363448	A	G	38	GENIC	homozygous	52067467
9	98363493	98363494	T	C	37	GENIC	homozygous	52067470
9	98363683	98363684	T	C	30	GENIC	homozygous	52443035
9	98364274	98364275	G	A	39	GENIC	homozygous	52443038
9	98364291	98364292	A	T	38	GENIC	homozygous	52443040
9	98364444	98364445	T	C	18	GENIC	homozygous	52443042
9	98364614	98364615	A	G	21	GENIC	homozygous	52067476
9	98364822	98364823	A	G	17	GENIC	homozygous	52443044