chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	73236494	73236495	C	G	21	GENIC	homozygous	51494046
10	73240896	73240897	A	G	9	GENIC	homozygous	51494051
10	73242770	73242771	A	G	16	GENIC	homozygous	51494054
10	73244290	73244291	G	C	10	GENIC	homozygous	51494055
10	73244945	73244946	C	G	12	GENIC	homozygous	53529329
10	73246782	73246783	T	C	14	GENIC	homozygous	53529331
10	73239217	73239218	C	T	7	GENIC	homozygous	53529327
10	73242411	73242413	TT	--	15	GENIC	homozygous	53529328
10	73246775	73246776	C	G	12	GENIC	homozygous	53529330
10	73249352	73249353	A	C	19	GENIC	homozygous	51494059
10	73250120	73250121	G	T	21	GENIC	homozygous	53529332
10	73250121	73250122	C	T	21	GENIC	homozygous	53529333
10	73250122	73250123	A	T	21	GENIC	homozygous	53529334
10	73250195	73250196	G	T	14	GENIC	homozygous	51494061
10	73250496	73250497	C	A	13	GENIC	homozygous	53529335
10	73252027	73252028	A	-	8	GENIC	homozygous	53529336
10	73252302	73252303	G	A	8	GENIC	homozygous	53529337
10	73254013	73254014	T	C	17	GENIC	homozygous	51494069
10	73254192	73254193	T	C	23	GENIC	homozygous	51494070
10	73254746	73254747	T	C	13	GENIC	homozygous	51494072
10	73256863	73256864	T	C	14	GENIC	homozygous	51494077
10	73258370	73258371	G	T	19	GENIC	homozygous	51494079
10	73258831	73258832	C	-	17	GENIC	homozygous	51494081
10	73263791	73263792	C	G	8	GENIC	homozygous	53529338
10	73263795	73263796	C	G	8	GENIC	homozygous	51494083