chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	11002430	11002431	T	G	33	GENIC	homozygous	144413776
10	11003518	11003519	A	G	17	GENIC	homozygous	144413777
10	11004942	11004943	T	C	23	GENIC	homozygous	144413778
10	11006865	11006866	C	T	18	GENIC	homozygous	144413779
10	11003780	11003781	C	G	16	GENIC	homozygous	142213466
10	11008147	11008148	T		7	GENIC	heterozygous	403276153
10	11008147	11008148	T	G	7	GENIC	possibly homozygous	403276154
10	11008164	11008165	T	G	9	GENIC	homozygous	403276155
10	11009193	11009194	C	T	21	GENIC	homozygous	144413780
10	11009267	11009268	G	A	27	GENIC	homozygous	144413781
10	11009352	11009353	T	C	19	GENIC	homozygous	142213471
10	11009708	11009709	G		5	GENIC	homozygous	403276156
10	11009708	11009709	G	T	5	GENIC	heterozygous	403276157
10	11010624	11010625	A	G	17	GENIC	homozygous	142213473
10	11018388	11018389	T	C	33	GENIC	homozygous	142213478
10	11014272	11014272		CTC	32	GENIC	homozygous	142195983
10	11015772	11015772		G	22	GENIC	homozygous	142195984