chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	110139141	110139142	A	-	13	GENIC	homozygous	52684191
10	110139153	110139154	A	G	18	GENIC	homozygous	52814776
10	110139500	110139501	C	T	43	GENIC	homozygous	51601059
10	110140004	110140007	AAA	---	15	GENIC	homozygous	51601060
10	110140154	110140155	A	G	28	GENIC	homozygous	51601062
10	110140346	110140347	A	-	13	GENIC	homozygous	51601063
10	110140426	110140427	A	AGG	2	GENIC	heterozygous	52814779
10	110140635	110140636	A	G	12	GENIC	homozygous	51601064
10	110140738	110140739	G	A	14	GENIC	homozygous	51601065
10	110140784	110140785	G	T	15	GENIC	possibly homozygous	51601066
10	110142723	110142725	AA	--	18	INTERGENIC	homozygous	51601067
10	110142859	110142860	T	C	21	INTERGENIC	possibly homozygous	51601068
10	110145666	110145667	T	C	28	GENIC	possibly homozygous	51601069
10	110146190	110146191	A	G	27	GENIC	possibly homozygous	51601070
10	110147331	110147332	G	A	26	GENIC	possibly homozygous	51601073
10	110147657	110147658	C	A	34	GENIC	possibly homozygous	51601074
10	110147827	110147828	A	C	38	GENIC	homozygous	51601075