chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	118370430	118370431	A	G	28	GENIC	homozygous	52832128
8	118371767	118371768	C	CAA	13	GENIC	heterozygous	52832129
8	118371767	118371768	C	CAAA	13	GENIC	heterozygous	52832130
8	118371892	118371893	G	A	19	GENIC	homozygous	52832131
8	118372392	118372393	G	A	38	GENIC	homozygous	52832132
8	118373559	118373560	G	A	30	GENIC	homozygous	52832133
8	118373984	118373985	A	G	31	GENIC	homozygous	52832134
8	118374062	118374063	G	C	20	GENIC	heterozygous	52832135
8	118374155	118374156	G	A	23	GENIC	homozygous	52832136
8	118374344	118374345	A	G	35	GENIC	homozygous	52832137
8	118374392	118374393	A	G	46	GENIC	homozygous	52832138
8	118374568	118374569	G	A	32	GENIC	homozygous	52832139
8	118375015	118375018	TGG	---	20	GENIC	homozygous	52832140
8	118375118	118375119	C	-	26	GENIC	homozygous	52832141
8	118375141	118375142	T	C	21	GENIC	homozygous	52832142
8	118375786	118375787	C	CTCCTCCCA	18	GENIC	possibly homozygous	52832143
8	118375799	118375800	T	C	27	GENIC	heterozygous	53183510
8	118375809	118375810	T	C	25	GENIC	possibly homozygous	52832144