chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	28967075	28967076	A	C	34	GENIC	homozygous	50705028
11	28968232	28968233	T	C	46	GENIC	homozygous	50705032
11	28969011	28969012	C	T	65	GENIC	possibly homozygous	50996758
11	28969441	28969442	A	G	41	GENIC	homozygous	50705034
11	28971182	28971183	C	A	38	GENIC	homozygous	50996759
11	28971573	28971574	A	G	35	GENIC	homozygous	50705036
11	28972868	28972869	G	T	32	GENIC	homozygous	50996760
11	28972939	28972940	T	G	35	GENIC	homozygous	50705038
11	28972956	28972957	A	T	37	GENIC	homozygous	50996761
11	28973129	28973130	A	T	30	GENIC	homozygous	50705040
11	28973543	28973544	T	C	46	GENIC	homozygous	50705042
11	28974268	28974269	C	T	36	GENIC	homozygous	50705044
11	28974670	28974671	A	AT	18	GENIC	homozygous	50705050
11	28974690	28974693	AGT	---	15	GENIC	homozygous	50705052
11	28974719	28974720	C	T	18	GENIC	homozygous	50705054