chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	81816574	81816575	T	C	39	GENIC	homozygous	111637178
3	81821237	81821238	G	C	52	GENIC	homozygous	111637179
3	81822733	81822734	C	T	28	GENIC	homozygous	111637181
3	81825915	81825916	A	G	38	GENIC	homozygous	111637182
3	81826984	81826985	C	T	29	GENIC	homozygous	111637184
3	81828252	81828253	A	G	25	GENIC	homozygous	111637185
3	81828989	81828990	G	A	19	GENIC	homozygous	111637187
3	81830132	81830133	G	A	30	GENIC	homozygous	111637189
3	81831216	81831217	G	A	44	GENIC	homozygous	111637190
3	81831220	81831221	A	C	43	GENIC	homozygous	111637192
3	81831397	81831398	T	C	28	GENIC	homozygous	111637193
3	81831501	81831502	T	C	29	GENIC	homozygous	111637195
3	81834085	81834086	C	T	44	GENIC	homozygous	111637197
3	81835245	81835246	A	C	16	GENIC	homozygous	111637198
3	81836330	81836331	C	T	45	GENIC	homozygous	111637203
3	81836696	81836697	A	G	41	GENIC	homozygous	111637204
3	81838814	81838815	C	T	26	GENIC	homozygous	111637206
3	81839342	81839343	T	C	25	GENIC	homozygous	111637208
3	81841760	81841761	C	T	22	GENIC	homozygous	111637209
3	81842781	81842782	A	G	41	GENIC	homozygous	111637211
3	81843034	81843035	T	A	51	GENIC	homozygous	111637212
3	81845613	81845614	A	T	29	GENIC	homozygous	111637214
3	81846918	81846919	T	G	15	GENIC	homozygous	111637216
3	81846980	81846981	T	C	27	GENIC	homozygous	111637217
3	81847500	81847501	G	A	41	GENIC	homozygous	111637219
3	81850107	81850108	G	A	22	GENIC	homozygous	111637220
3	81851016	81851017	C	T	27	GENIC	homozygous	111637222
3	81851996	81851997	T	A	32	GENIC	homozygous	111637224