chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	90793859	90793860	G	A	16	GENIC	homozygous	116904975
10	90793886	90793887	G	A	13	GENIC	homozygous	116904977
10	90793922	90793923	C	T	10	GENIC	homozygous	116904979
10	90793939	90793940	G	A	11	GENIC	homozygous	116676988
10	90794673	90794674	G	A	27	GENIC	homozygous	117228009
10	90794688	90794689	T	A	29	GENIC	homozygous	117228011
10	90794689	90794690	A	G	29	GENIC	homozygous	117228013
10	90794690	90794691	T	G	29	GENIC	homozygous	117228015
10	90794694	90794695	G	A	29	GENIC	homozygous	117228017
10	90794998	90794999	A	C	6	GENIC	homozygous	117197777
10	90795648	90795649	T	A	16	GENIC	homozygous	116904981
10	90795671	90795672	G	C	14	GENIC	homozygous	116676990
10	90795672	90795673	C	A	14	GENIC	homozygous	116676992
10	90795791	90795792	G	C	11	GENIC	homozygous	116676996
10	90795967	90795968	T	A	20	GENIC	homozygous	116677000
10	90795991	90795992	C	G	24	GENIC	homozygous	116677002
10	90796024	90796025	A	G	11	GENIC	homozygous	116677004
10	90796045	90796046	C	A	18	GENIC	homozygous	116677006
10	90796173	90796174	G	A	36	GENIC	homozygous	116677008
10	90796176	90796177	A	T	33	GENIC	homozygous	116677010