chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	181766668	181766669	C	T	10	GENIC	homozygous	60989200
1	181766773	181766775	AA	--	15	GENIC	homozygous	60989202
1	181766902	181766903	T	C	21	GENIC	homozygous	60989204
1	181767034	181767035	G	A	26	GENIC	homozygous	60989206
1	181767200	181767201	A	G	39	GENIC	homozygous	60989208
1	181767700	181767701	T	TGCG	12	GENIC	homozygous	60989210
1	181768782	181768783	C	T	26	GENIC	homozygous	60989212
1	181775766	181775767	T	TATCCATCTATCCATCC	18	GENIC	heterozygous	62180263
1	181775888	181775889	G	A	29	GENIC	homozygous	61564914
1	181778462	181778463	A	-	10	GENIC	homozygous	60989225
1	181779472	181779473	T	TC	26	GENIC	homozygous	60989227
1	181779861	181779862	G	A	33	GENIC	homozygous	60989229
1	181780175	181780176	A	G	29	GENIC	homozygous	60989231
1	181780692	181780696	AAAA	----	6	GENIC	heterozygous	62180265
1	181780939	181780940	A	C	33	GENIC	homozygous	60989235
1	181780940	181780941	T	A	33	GENIC	homozygous	60989237
1	181781294	181781295	G	A	31	GENIC	homozygous	60989239
1	181781667	181781668	T	C	20	GENIC	homozygous	60989241
1	181784053	181784056	TTC	---	19	GENIC	homozygous	61564917
1	181787445	181787446	G	A	10	GENIC	homozygous	60989247
1	181788532	181788533	A	G	18	GENIC	homozygous	60989249
1	181789505	181789506	T	-	6	GENIC	heterozygous	62180267