chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	110139140	110139141	A	-	23	GENIC	possibly homozygous	51601058
10	110139500	110139501	C	T	47	GENIC	homozygous	51601059
10	110140004	110140007	AAA	---	27	GENIC	homozygous	51601060
10	110140015	110140019	AAAT	----	26	GENIC	possibly homozygous	51601061
10	110140154	110140155	A	G	39	GENIC	homozygous	51601062
10	110140346	110140347	A	-	25	GENIC	homozygous	51601063
10	110140635	110140636	A	G	36	GENIC	homozygous	51601064
10	110140738	110140739	G	A	38	GENIC	homozygous	51601065
10	110140784	110140785	G	T	34	GENIC	homozygous	51601066
10	110142723	110142725	AA	--	32	INTERGENIC	possibly homozygous	51601067
10	110142859	110142860	T	C	38	INTERGENIC	homozygous	51601068
10	110145666	110145667	T	C	22	GENIC	homozygous	51601069
10	110146190	110146191	A	G	22	GENIC	homozygous	51601070
10	110147003	110147004	T	TG	8	GENIC	homozygous	51601071
10	110147010	110147011	C	-	9	GENIC	heterozygous	51601072
10	110147331	110147332	G	A	44	GENIC	homozygous	51601073
10	110147657	110147658	C	A	53	GENIC	homozygous	51601074
10	110147827	110147828	A	C	29	GENIC	homozygous	51601075
10	110142724	110142725	A	-	32	INTERGENIC	heterozygous	51774840