chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	94280849	94280850	T	G	9	GENIC	homozygous	116685012
10	94280853	94280854	T	C	7	GENIC	homozygous	116685014
10	94280904	94280905	C	G	14	GENIC	possibly homozygous	116685016
10	94284680	94284681	A	G	46	GENIC	homozygous	116685020
10	94285636	94285637	A	C	34	GENIC	homozygous	116685022
10	94287037	94287038	A	G	39	GENIC	homozygous	116685024
10	94286819	94286820	G	A	24	GENIC	homozygous	118009247
10	94286946	94286947	A	G	42	GENIC	possibly homozygous	118009248
10	94287328	94287329	A	T	48	GENIC	homozygous	116685026
10	94287433	94287434	G	T	50	GENIC	homozygous	116685028
10	94289092	94289093	C	G	33	GENIC	homozygous	116685030
10	94304714	94304715	C	T	36	GENIC	homozygous	116685032
10	94306759	94306760	G	A	27	GENIC	homozygous	116685034
10	94313480	94313481	C	T	40	GENIC	homozygous	116685036
10	94314877	94314878	A	T	33	GENIC	heterozygous	118009249
10	94317777	94317778	C	T	20	GENIC	homozygous	118009250
10	94326992	94326993	C	G	46	GENIC	homozygous	116685038
10	94327891	94327892	C	T	29	GENIC	homozygous	116685040
10	94332017	94332018	T	G	41	GENIC	heterozygous	118009251
10	94332251	94332252	G	A	45	GENIC	possibly homozygous	118009252
10	94337933	94337934	G	A	32	GENIC	homozygous	116685042
10	94345719	94345720	G	A	40	GENIC	heterozygous	116954851
10	94346186	94346187	A	G	47	GENIC	homozygous	116685046
10	94346565	94346566	G	A	52	GENIC	homozygous	116685048
10	94347781	94347782	G	A	45	GENIC	homozygous	116685050