chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	56703963	56703964	A	-	26	GENIC	homozygous	53388103
8	56704499	56704500	G	A	19	GENIC	homozygous	53341628
8	56704854	56704855	G	GT	11	GENIC	homozygous	52650716
8	56706184	56706185	C	T	19	GENIC	homozygous	52650719
8	56706888	56706889	G	GA	8	GENIC	heterozygous	53121194
8	56708162	56708163	C	T	19	GENIC	homozygous	53341630
8	56708561	56708562	G	GA	14	GENIC	heterozygous	53121195
8	56708561	56708562	G	GAAA	14	GENIC	heterozygous	53388104
8	56708566	56708567	A	-	14	GENIC	possibly homozygous	53388105
8	56709389	56709390	C	T	12	GENIC	homozygous	53341632
8	56709425	56709426	C	CAA	7	GENIC	homozygous	52980152
8	56709923	56709924	A	-	11	GENIC	homozygous	52980153
8	56710197	56710198	C	CTT	6	GENIC	homozygous	53388106
8	56715498	56715499	G	GTTAAAAACA	18	GENIC	homozygous	53388107
8	56717009	56717010	T	-	9	GENIC	homozygous	52650771
8	56720712	56720713	A	G	21	GENIC	homozygous	52650783
8	56720762	56720763	G	A	32	GENIC	homozygous	52650788
8	56720896	56720897	T	G	27	GENIC	homozygous	53341634
8	56722231	56722232	A	G	18	GENIC	homozygous	52650799
8	56723054	56723055	C	T	28	GENIC	homozygous	53341636
8	56723574	56723575	C	CT	17	GENIC	homozygous	52650808
8	56724972	56724973	A	-	24	GENIC	homozygous	52650814
8	56733567	56733569	TA	--	10	GENIC	homozygous	53388108
8	56733962	56733963	C	T	19	GENIC	homozygous	52650842
8	56734908	56734909	T	A	17	GENIC	homozygous	53341638
8	56735246	56735247	G	GC	14	GENIC	homozygous	52650854
8	56735482	56735483	G	A	30	GENIC	homozygous	53341640