chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	4941508	4941509	C	T	26	GENIC	possibly homozygous	117209987
9	4942361	4942362	T	A	13	GENIC	homozygous	117209988
9	4943251	4943252	G	A	22	GENIC	homozygous	117209989
9	4943776	4943777	C	T	19	GENIC	homozygous	117209990
9	4944083	4944084	T	C	33	GENIC	homozygous	117209991
9	4944329	4944330	A	G	27	GENIC	possibly homozygous	117209992
9	4944446	4944447	G	C	23	GENIC	possibly homozygous	117209993
9	4944711	4944712	G	A	27	GENIC	homozygous	117209994
9	4945417	4945418	A	C	30	GENIC	homozygous	117209995
9	4945685	4945686	G	A	35	GENIC	homozygous	117209996
9	4945847	4945848	T	C	27	GENIC	homozygous	117209997
9	4945872	4945873	A	G	19	GENIC	homozygous	117209998
9	4946085	4946086	T	C	26	GENIC	possibly homozygous	117209999
9	4946213	4946214	A	T	27	GENIC	homozygous	117210000
9	4948725	4948726	T	A	24	GENIC	homozygous	117210003
9	4948862	4948863	G	A	26	GENIC	homozygous	117210004
9	4950453	4950454	A	G	38	GENIC	homozygous	117210005
9	4961023	4961024	T	C	21	GENIC	possibly homozygous	117210015
9	4961402	4961403	G	C	30	GENIC	possibly homozygous	117210016
9	4962952	4962953	T	C	21	GENIC	homozygous	117210017
9	4963585	4963586	A	T	18	GENIC	homozygous	117210018
9	4963827	4963828	A	C	29	GENIC	homozygous	117210019
9	4963927	4963928	C	T	19	GENIC	homozygous	117210020
9	4966000	4966001	G	C	15	GENIC	homozygous	117210021
9	4967749	4967750	T	A	19	GENIC	homozygous	117210022
9	4968839	4968840	T	C	20	GENIC	possibly homozygous	117210023
9	4969786	4969787	A	T	20	GENIC	homozygous	117210024
9	4970188	4970189	C	G	10	GENIC	homozygous	117210026
9	4973752	4973753	A	C	13	GENIC	homozygous	117210027
9	4973911	4973912	A	G	15	GENIC	homozygous	117210028
9	4975159	4975160	G	A	19	GENIC	homozygous	117210030
9	4976823	4976824	C	T	13	GENIC	possibly homozygous	117210031
9	4976917	4976918	C	G	17	GENIC	homozygous	117210032
9	4977379	4977380	C	A	21	GENIC	homozygous	117210033
9	4977532	4977533	C	T	29	GENIC	homozygous	117210034
9	4977984	4977985	A	G	26	GENIC	homozygous	117210035