chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	122382884	122382885	C	T	32	GENIC	homozygous	116690213
8	122382894	122382895	C	T	33	GENIC	homozygous	116690215
8	122382896	122382897	T	C	34	GENIC	homozygous	116690217
8	122383356	122383357	C	T	21	GENIC	homozygous	116690219
8	122383721	122383722	C	T	37	GENIC	homozygous	116690221
8	122383786	122383787	T	G	34	GENIC	homozygous	116690223
8	122383799	122383800	T	A	36	GENIC	homozygous	116690225
8	122383862	122383863	T	C	32	GENIC	homozygous	116690227
8	122383923	122383924	G	A	27	GENIC	homozygous	116690229
8	122383936	122383937	G	C	28	GENIC	homozygous	116690231
8	122383984	122383985	C	T	25	GENIC	homozygous	116690233
8	122384064	122384065	G	A	25	GENIC	homozygous	116690235
8	122384155	122384156	A	C	26	GENIC	homozygous	116690237
8	122384204	122384205	A	C	21	GENIC	homozygous	116895093
8	122384319	122384320	A	C	3	GENIC	homozygous	118130520
8	122384503	122384504	C	T	28	GENIC	homozygous	116690247
8	122384566	122384567	A	C	39	GENIC	homozygous	116690249
8	122384766	122384767	T	C	35	GENIC	homozygous	116690251
8	122384849	122384850	C	T	26	GENIC	homozygous	116690253
8	122384897	122384898	T	C	21	GENIC	homozygous	116690255
8	122384945	122384946	A	T	17	GENIC	homozygous	117912805
8	122385429	122385430	T	C	24	GENIC	homozygous	116690261
8	122385664	122385665	C	T	30	GENIC	homozygous	116690263