chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	122197416	122197417	C	A	10	GENIC	homozygous	117954352
8	122198099	122198100	A	G	13	GENIC	homozygous	117954353
8	122201249	122201250	A	C	28	GENIC	homozygous	117954354
8	122204585	122204586	A	G	38	GENIC	homozygous	117954355
8	122213511	122213512	T	A	21	GENIC	homozygous	117954356
8	122214872	122214873	A	C	26	GENIC	homozygous	117954357
8	122221166	122221167	G	T	13	GENIC	homozygous	116689788
8	122221857	122221858	A	G	26	GENIC	homozygous	117954358
8	122222228	122222229	T	G	37	GENIC	homozygous	117954359
8	122223527	122223528	A	G	17	GENIC	homozygous	117954360
8	122226268	122226269	C	T	33	GENIC	homozygous	117954361
8	122226633	122226634	C	T	31	GENIC	homozygous	117954362
8	122227699	122227700	G	A	24	GENIC	homozygous	117954363
8	122227762	122227763	T	C	32	GENIC	homozygous	117954364
8	122227793	122227794	A	G	26	GENIC	homozygous	117954365
8	122232970	122232971	C	A	41	GENIC	homozygous	117954366
8	122233428	122233429	T	G	27	GENIC	homozygous	117954367
8	122233647	122233648	C	T	35	GENIC	homozygous	117954368
8	122237349	122237350	T	G	27	GENIC	homozygous	117954369
8	122238286	122238287	C	T	29	GENIC	homozygous	116689791
8	122240945	122240946	C	T	30	GENIC	homozygous	117954370