chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	50391286	50391287	T	C	18	GENIC	homozygous	115352147
12	50391862	50391863	C	T	32	GENIC	possibly homozygous	115352149
12	50392040	50392041	A	G	20	GENIC	homozygous	115352151
12	50393835	50393836	C	T	27	GENIC	homozygous	115352153
12	50394462	50394463	T	G	28	GENIC	homozygous	115352155
12	50394701	50394702	T	C	17	GENIC	homozygous	115352157
12	50395330	50395331	A	G	14	GENIC	homozygous	115352159
12	50396070	50396071	G	A	30	GENIC	homozygous	115352161
12	50397341	50397342	A	G	16	GENIC	homozygous	115352163
12	50397771	50397772	G	T	22	GENIC	homozygous	115352165
12	50397837	50397838	G	A	22	GENIC	homozygous	115352167
12	50398365	50398366	A	G	33	GENIC	homozygous	115352169
12	50398534	50398535	T	A	22	GENIC	homozygous	115352171
12	50398698	50398699	C	T	25	GENIC	homozygous	115403546
12	50398830	50398831	G	A	33	GENIC	homozygous	115403548
12	50399025	50399026	C	T	30	GENIC	homozygous	115352173
12	50399183	50399184	A	G	33	GENIC	homozygous	115352175
12	50399372	50399373	C	T	48	GENIC	homozygous	115352177
12	50399685	50399686	G	A	33	GENIC	homozygous	115352181
12	50400570	50400571	A	T	29	GENIC	homozygous	115352183
12	50400602	50400603	A	G	20	GENIC	homozygous	115352185
12	50401260	50401261	G	A	21	GENIC	homozygous	115352187
12	50401276	50401277	C	T	19	GENIC	homozygous	115352189
12	50401732	50401733	C	T	27	GENIC	homozygous	115352191
12	50401950	50401951	A	G	32	GENIC	homozygous	115352193
12	50402025	50402026	G	A	26	GENIC	homozygous	115352195
12	50403645	50403646	T	C	40	GENIC	homozygous	115352197
12	50404278	50404279	G	A	28	GENIC	homozygous	115352199
12	50404316	50404317	C	T	28	GENIC	homozygous	115352201
12	50404413	50404414	T	C	19	GENIC	homozygous	115352203