chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	50394141	50394142	G	A	28	GENIC	homozygous	50032151
13	50394665	50394673	ATATATAT	--------	20	GENIC	homozygous	50032153
13	50395629	50395630	G	A	33	GENIC	homozygous	50032155
13	50395793	50395794	C	G	29	GENIC	homozygous	50032157
13	50395835	50395836	A	G	36	GENIC	homozygous	50032159
13	50395948	50395952	CGGT	----	24	GENIC	homozygous	50032161
13	50395953	50395954	G	A	24	GENIC	homozygous	50601981
13	50396090	50396091	G	GAAGA	22	GENIC	possibly homozygous	50032163
13	50396107	50396109	CG	--	31	GENIC	homozygous	50032165
13	50396245	50396246	C	T	31	GENIC	homozygous	50032169
13	50396367	50396369	TT	--	18	GENIC	homozygous	50032171
13	50396391	50396392	G	GT	22	GENIC	homozygous	50032173
13	50396455	50396456	A	G	41	GENIC	homozygous	50032175
13	50396769	50396770	G	A	23	GENIC	homozygous	50032177
13	50396948	50396949	T	C	34	GENIC	homozygous	50032179
13	50396959	50396960	A	-	31	GENIC	homozygous	50032181
13	50397254	50397255	G	T	22	GENIC	homozygous	50032183
13	50397295	50397296	C	CG	11	GENIC	homozygous	50032185
13	50397618	50397619	A	G	26	GENIC	homozygous	50032187
13	50397907	50397908	G	T	18	GENIC	homozygous	50032189