chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	28966884	28966885	G	A	20	GENIC	homozygous	50705024
11	28966980	28966981	C	T	28	GENIC	homozygous	50705026
11	28967075	28967076	A	C	38	GENIC	possibly homozygous	50705028
11	28967716	28967717	C	T	24	GENIC	possibly homozygous	50705030
11	28968232	28968233	T	C	18	GENIC	homozygous	50705032
11	28969441	28969442	A	G	24	GENIC	homozygous	50705034
11	28971573	28971574	A	G	30	GENIC	homozygous	50705036
11	28972939	28972940	T	G	22	GENIC	homozygous	50705038
11	28973129	28973130	A	T	13	GENIC	homozygous	50705040
11	28973543	28973544	T	C	27	GENIC	possibly homozygous	50705042
11	28974268	28974269	C	T	37	GENIC	possibly homozygous	50705044
11	28974351	28974352	T	C	19	GENIC	possibly homozygous	50705046
11	28974527	28974528	T	TGGTTAGAC	21	GENIC	possibly homozygous	50705048
11	28974670	28974671	A	AT	4	GENIC	homozygous	50705050
11	28974690	28974693	AGT	---	9	GENIC	homozygous	50705052
11	28974719	28974720	C	T	12	GENIC	possibly homozygous	50705054