chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	110140024	110140025	C	T	18	GENIC	homozygous	51958641
10	110140154	110140155	A	G	21	GENIC	homozygous	51601062
10	110140346	110140347	A	-	21	GENIC	homozygous	51601063
10	110140427	110140428	G	-	3	GENIC	homozygous	51958644
10	110140631	110140632	G	C	4	GENIC	homozygous	51958647
10	110140635	110140636	A	G	4	GENIC	homozygous	51601064
10	110141328	110141342	GTCGTCAGTGCTGC	--------------	7	GENIC	homozygous	52331909
10	110142102	110142103	A	C	22	INTERGENIC	homozygous	51958653
10	110142724	110142725	A	-	16	INTERGENIC	possibly homozygous	51774840
10	110142859	110142860	T	C	42	INTERGENIC	homozygous	51601068
10	110145666	110145667	T	C	26	GENIC	homozygous	51601069
10	110147057	110147058	C	CTTTT	5	GENIC	homozygous	51958658
10	110147376	110147377	T	A	28	GENIC	homozygous	51958661
10	110147657	110147658	C	A	32	GENIC	homozygous	51601074
10	110147827	110147828	A	C	25	GENIC	homozygous	51601075
10	110147935	110147936	G	A	26	GENIC	homozygous	51958664