chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	26859464	26859465	T	G	27	GENIC	homozygous	111769726
16	26860020	26860021	T	C	33	GENIC	homozygous	112259343
16	26861756	26861757	G	A	42	GENIC	homozygous	111769728
16	26863886	26863887	A	C	57	GENIC	homozygous	111769730
16	26866586	26866587	G	A	37	GENIC	homozygous	111769732
16	26868756	26868757	T	C	56	GENIC	homozygous	111769734
16	26869896	26869897	C	T	50	GENIC	homozygous	111769736
16	26869948	26869949	C	G	46	GENIC	homozygous	111769738
16	26869983	26869984	C	A	42	GENIC	homozygous	111769740
16	26870044	26870045	G	A	22	GENIC	homozygous	111769742
16	26870374	26870375	C	T	32	GENIC	homozygous	111769744
16	26871080	26871081	C	T	46	GENIC	homozygous	111769746
16	26871818	26871819	C	A	23	GENIC	homozygous	111769748
16	26872590	26872591	T	G	37	GENIC	homozygous	111769750
16	26873169	26873170	T	C	28	GENIC	possibly homozygous	111769752
16	26862906	26862907	C	T	37	GENIC	homozygous	112152885
16	26874236	26874237	A	G	58	GENIC	homozygous	111769754
16	26874261	26874262	T	C	65	GENIC	homozygous	111769756
16	26874355	26874356	T	C	44	GENIC	homozygous	111769758
16	26874661	26874662	T	C	56	GENIC	homozygous	111769760
16	26875802	26875803	G	A	23	GENIC	homozygous	111769762
16	26866976	26866977	G	C	13	GENIC	homozygous	119104708