chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	53012570	53012571	A	AG	2	GENIC	homozygous	50193447
13	53015273	53015274	C	-	32	GENIC	homozygous	49758401
13	53015459	53015460	G	GT	32	GENIC	homozygous	49758402
13	53015788	53015789	G	C	39	GENIC	homozygous	49949159
13	53015937	53015940	CCA	---	5	GENIC	heterozygous	50041293
13	53015938	53015940	CA	--	5	GENIC	heterozygous	49949160
13	53015982	53015983	G	A	19	GENIC	homozygous	49949161
13	53017716	53017717	A	G	48	GENIC	homozygous	49949162
13	53018521	53018522	C	T	27	GENIC	homozygous	49949163
13	53018795	53018796	A	AAGAT	26	GENIC	homozygous	49949164
13	53020186	53020187	T	C	35	GENIC	heterozygous	49949165
13	53020186	53020187	T	TC	27	GENIC	heterozygous	49949166
13	53022376	53022377	T	A	51	GENIC	homozygous	49949167
13	53023441	53023442	G	A	41	GENIC	homozygous	49949168
13	53024206	53024207	C	T	35	GENIC	possibly homozygous	49949169
13	53024927	53024928	T	C	51	GENIC	homozygous	49949170
13	53025564	53025565	T	C	41	GENIC	homozygous	49949171
13	53025954	53025955	T	C	32	GENIC	heterozygous	49758403
13	53025995	53025996	T	C	32	GENIC	homozygous	49758404
13	53026020	53026021	T	C	45	GENIC	homozygous	49949172
13	53026443	53026444	A	C	45	GENIC	homozygous	49949173
13	53026711	53026712	C	CCTTAT	27	GENIC	homozygous	49949174
13	53026956	53026957	A	G	43	GENIC	homozygous	49949175
13	53027521	53027522	C	T	34	GENIC	homozygous	49949176
13	53028367	53028368	G	A	31	GENIC	homozygous	49949177
13	53029473	53029474	A	G	39	GENIC	homozygous	49949179
13	53029651	53029652	A	G	33	GENIC	homozygous	49949180
13	53030119	53030120	C	G	28	GENIC	homozygous	49949181
13	53030916	53030917	A	G	16	GENIC	possibly homozygous	50041328
13	53033485	53033486	A	G	52	GENIC	homozygous	49949188
13	53033636	53033637	T	C	36	GENIC	homozygous	49949189
13	53027382	53027383	C	T	32	GENIC	homozygous	50230725
13	53031053	53031054	A	G	38	GENIC	homozygous	50230727