chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	98293998	98293999	G	-	15	GENIC	heterozygous	51561650
10	98294002	98294003	C	CA	6	GENIC	heterozygous	51561652
10	98298176	98298177	A	G	27	GENIC	heterozygous	51561665
10	98298199	98298200	T	G	30	GENIC	heterozygous	51561667
10	98298213	98298214	T	A	31	GENIC	heterozygous	51561668
10	98298219	98298220	G	A	33	GENIC	heterozygous	51561670
10	98300338	98300339	T	-	1	GENIC	homozygous	51753612
10	98300585	98300586	C	CT	1	GENIC	homozygous	51561676
10	98301247	98301249	TT	--	7	GENIC	heterozygous	51561680
10	98304200	98304201	A	-	19	GENIC	heterozygous	51753614
10	98307991	98307995	ACAC	----	9	GENIC	homozygous	51753616
10	98315125	98315127	AC	--	13	GENIC	heterozygous	51753620
10	98330010	98330011	A	G	21	GENIC	possibly homozygous	51561845
10	98331424	98331425	A	G	12	GENIC	heterozygous	52168507
10	98334339	98334340	A	AAC	12	GENIC	possibly homozygous	51561853
10	98337850	98337851	T	C	12	GENIC	heterozygous	51561863
10	98337851	98337852	G	C	12	GENIC	heterozygous	51561865
10	98338036	98338037	A	T	42	GENIC	heterozygous	51561867
10	98338074	98338075	A	T	38	GENIC	heterozygous	51561869
10	98338080	98338081	A	G	38	GENIC	heterozygous	51561871
10	98346746	98346747	G	-	6	GENIC	heterozygous	51561935