chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	94302276	94302277	G	T	40	GENIC	homozygous	117605035
9	94302590	94302591	G	A	49	GENIC	homozygous	117605037
9	94302760	94302760		G	29	GENIC	homozygous	128733214
9	94303107	94303108	C	T	53	GENIC	homozygous	117605039
9	94303388	94303507	AACAAAAAGAGAGCAGGGGGGCTGGGGATTTAGCTCAGTGGTAGAACGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAGAACCAAAAAAAAAACAAA		24	GENIC	possibly homozygous	128733215
9	94306113	94306114	A		57	GENIC	homozygous	128733216
9	94306123	94306124	A		55	GENIC	homozygous	128733217
9	94306125	94306126	A	G	55	GENIC	homozygous	117605043
9	94306138	94306139	C	A	58	GENIC	homozygous	117605045
9	94306140	94306141	T	C	58	GENIC	homozygous	117605047
9	94307058	94307059	A	G	61	GENIC	homozygous	117605049
9	94303358	94303359	G	A	30	GENIC	homozygous	117601999
9	94303703	94303704	G	A	59	GENIC	homozygous	117602001
9	94306008	94306009	G	C	70	GENIC	homozygous	117602003
9	94307796	94307797	G	A	61	GENIC	homozygous	117602005
9	94304517	94304517		A	44	GENIC	homozygous	132135240