chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	181766668	181766669	C	T	12	GENIC	homozygous	60989200
1	181766773	181766775	AA	--	17	GENIC	homozygous	60989202
1	181766902	181766903	T	C	9	GENIC	possibly homozygous	60989204
1	181767034	181767035	G	A	12	GENIC	homozygous	60989206
1	181767200	181767201	A	G	13	GENIC	homozygous	60989208
1	181767700	181767701	T	TGCG	4	GENIC	homozygous	60989210
1	181768782	181768783	C	T	18	GENIC	possibly homozygous	60989212
1	181775888	181775889	G	A	27	GENIC	possibly homozygous	61564914
1	181778462	181778463	A	-	1	GENIC	homozygous	60989225
1	181779472	181779473	T	TC	8	GENIC	possibly homozygous	60989227
1	181779861	181779862	G	A	15	GENIC	homozygous	60989229
1	181780175	181780176	A	G	31	GENIC	homozygous	60989231
1	181780939	181780940	A	C	5	GENIC	homozygous	60989235
1	181780940	181780941	T	A	5	GENIC	homozygous	60989237
1	181781294	181781295	G	A	12	GENIC	homozygous	60989239
1	181781667	181781668	T	C	23	GENIC	possibly homozygous	60989241
1	181784053	181784056	TTC	---	2	GENIC	homozygous	61564917
1	181784444	181784445	A	-	6	GENIC	heterozygous	62092875
1	181787445	181787446	G	A	8	GENIC	heterozygous	60989247
1	181788532	181788533	A	G	19	GENIC	possibly homozygous	60989249