chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	116440435	116440436	A	G	25	GENIC	homozygous	116669365
8	116446650	116446651	A	G	43	GENIC	homozygous	116669367
8	116446979	116446980	G	A	29	GENIC	homozygous	116669369
8	116447427	116447428	T	C	26	GENIC	homozygous	116669371
8	116447513	116447514	T	C	34	GENIC	homozygous	116669373
8	116447898	116447899	T	C	32	GENIC	homozygous	116669375
8	116448516	116448517	C	T	31	GENIC	homozygous	116669377
8	116451919	116451920	A	C	28	GENIC	homozygous	116669379
8	116453888	116453889	G	A	33	GENIC	homozygous	116669381
8	116455245	116455246	G	A	39	GENIC	homozygous	116669383
8	116455668	116455669	G	A	34	GENIC	homozygous	116669385
8	116457201	116457202	A	G	33	GENIC	homozygous	116669387
8	116457906	116457907	C	T	17	GENIC	possibly homozygous	116669389
8	116461784	116461785	A	G	38	GENIC	homozygous	116669391
8	116462705	116462706	C	G	28	GENIC	homozygous	116669393
8	116463628	116463629	C	G	67	GENIC	heterozygous	116669395
8	116463905	116463906	C	G	72	GENIC	heterozygous	117188869
8	116463953	116463954	C	G	75	GENIC	heterozygous	116669397
8	116464151	116464152	T	C	29	GENIC	homozygous	116669399
8	116465370	116465371	T	C	39	GENIC	homozygous	116669401
8	116465391	116465392	G	A	39	GENIC	homozygous	116669403
8	116469257	116469258	G	A	33	GENIC	homozygous	116669405
8	116469327	116469328	C	G	36	GENIC	possibly homozygous	116669407
8	116469366	116469367	G	C	26	GENIC	homozygous	116669409