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	8	GENIC	homozygous	116685014
10	94280904	94280905	C	G	10	GENIC	homozygous	116685016
10	94280909	94280910	T	C	11	GENIC	homozygous	116685018
10	94284680	94284681	A	G	42	GENIC	homozygous	116685020
10	94285636	94285637	A	C	32	GENIC	homozygous	116685022
10	94287037	94287038	A	G	37	GENIC	homozygous	116685024
10	94287328	94287329	A	T	44	GENIC	homozygous	116685026
10	94287433	94287434	G	T	47	GENIC	homozygous	116685028
10	94289092	94289093	C	G	29	GENIC	homozygous	116685030
10	94304714	94304715	C	T	35	GENIC	homozygous	116685032
10	94306759	94306760	G	A	24	GENIC	homozygous	116685034
10	94313480	94313481	C	T	38	GENIC	homozygous	116685036
10	94326992	94326993	C	G	40	GENIC	homozygous	116685038
10	94327891	94327892	C	T	28	GENIC	homozygous	116685040
10	94337933	94337934	G	A	31	GENIC	homozygous	116685042
10	94342439	94342440	T	A	10	GENIC	possibly homozygous	116685044
10	94346186	94346187	A	G	37	GENIC	homozygous	116685046
10	94346565	94346566	G	A	43	GENIC	homozygous	116685048
10	94347781	94347782	G	A	40	GENIC	homozygous	116685050