chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	126376792	126376793	T	C	41	GENIC	homozygous	112826127
4	126376972	126376973	A	T	44	GENIC	homozygous	112826129
4	126377405	126377406	G	A	35	GENIC	homozygous	113301815
4	126382789	126382790	G	C	26	GENIC	heterozygous	113301816
4	126384009	126384010	T	C	36	GENIC	homozygous	113301817
4	126384668	126384669	T	C	53	GENIC	homozygous	113301818
4	126385446	126385447	A	C	36	GENIC	possibly homozygous	113301819
4	126385814	126385815	T	C	34	GENIC	homozygous	113301820
4	126385975	126385976	G	A	37	GENIC	homozygous	113301821
4	126386539	126386540	A	G	41	GENIC	homozygous	113301822
4	126388576	126388577	G	A	40	GENIC	homozygous	113301823
4	126389136	126389137	A	G	50	GENIC	homozygous	113301824
4	126389323	126389324	C	T	10	GENIC	heterozygous	113301825
4	126389326	126389327	C	T	9	GENIC	heterozygous	113301826
4	126390242	126390243	A	G	27	GENIC	possibly homozygous	113301827
4	126391330	126391331	G	A	65	GENIC	possibly homozygous	113301828
4	126393846	126393847	G	C	29	GENIC	possibly homozygous	113301829
4	126394116	126394117	A	G	36	GENIC	homozygous	113301830
4	126394351	126394352	G	A	24	GENIC	homozygous	113301831
4	126394470	126394471	G	C	27	GENIC	homozygous	113301832
4	126394985	126394986	G	A	42	GENIC	homozygous	113301833
4	126395165	126395166	C	T	42	GENIC	homozygous	113301834
4	126395189	126395190	G	C	39	GENIC	homozygous	113301835
4	126395271	126395272	C	A	32	GENIC	homozygous	113301836
4	126398668	126398669	G	T	55	GENIC	heterozygous	113301837
4	126399943	126399944	G	A	56	GENIC	possibly homozygous	113301838
4	126400682	126400683	T	C	17	GENIC	homozygous	113301839