chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	94983711	94983712	C	T	29	GENIC	homozygous	52055164
9	94984358	94984359	A	G	26	GENIC	homozygous	52055166
9	94984528	94984529	C	T	19	GENIC	possibly homozygous	52280960
9	94984892	94984893	T	A	38	GENIC	possibly homozygous	52055168
9	94985100	94985101	A	G	32	GENIC	homozygous	52055170
9	94985280	94985281	G	T	19	GENIC	homozygous	52055172
9	94985301	94985302	A	G	16	GENIC	homozygous	52055174
9	94985330	94985331	G	A	17	GENIC	homozygous	52055176
9	94985372	94985373	G	C	17	GENIC	homozygous	52055178
9	94985386	94985387	C	T	17	GENIC	homozygous	52055180
9	94986038	94986039	T	C	15	GENIC	homozygous	52055182
9	94986653	94986656	TAA	---	35	GENIC	possibly homozygous	52055188
9	94986941	94986942	C	A	19	GENIC	homozygous	52280961
9	94987889	94987890	G	GCA	19	GENIC	possibly homozygous	52280962
9	94987950	94987951	A	T	44	GENIC	homozygous	52280963
9	94989529	94989530	A	T	9	GENIC	homozygous	52055198
9	94989577	94989578	A	AT	5	GENIC	homozygous	52280964