chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	122004188	122004189	C	G	42	GENIC	homozygous	116689764
8	122039897	122039898	A	T	53	GENIC	homozygous	116689766
8	122053371	122053372	A	C	24	GENIC	homozygous	116988349
8	122055397	122055398	G	A	20	GENIC	homozygous	116689768
8	122056046	122056047	G	A	45	GENIC	homozygous	116689770
8	122056102	122056103	T	C	45	GENIC	homozygous	116689772
8	122056147	122056148	T		42	GENIC	homozygous	128640219
8	122057046	122057047	A	G	26	GENIC	heterozygous	116689776
8	122057046	122057046		G	27	GENIC	heterozygous	128640220
8	122062631	122062631		CTTTTTTCC	42	GENIC	homozygous	128640222
8	122066522	122066594	TTCCTGGGATTGAGAGTTCTTTTTTTTTTTTTAAGATTTATTCATTTATTATATATAAGTACACTGCAGCTG		16	GENIC	homozygous	128640223
8	122068148	122068149	T		39	GENIC	homozygous	128640225
8	122126673	122126674	C	T	38	GENIC	homozygous	116689778
8	122132577	122132578	G	T	50	GENIC	heterozygous	131061633
8	122132587	122132588	G	T	48	GENIC	heterozygous	131061634
8	122132589	122132590	A	G	49	GENIC	heterozygous	131061635
8	122095745	122095746	C	G	10	GENIC	heterozygous	117149838
8	122174255	122174256	G	C	46	GENIC	homozygous	116689784
8	122180542	122180543	C	T	46	GENIC	homozygous	116689786