chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	50391567	50391568	A	G	4	GENIC	homozygous	115403532
12	50392424	50392425	C	G	18	GENIC	homozygous	115403534
12	50393594	50393595	A	G	10	GENIC	homozygous	115403542
12	50394462	50394463	T	G	15	GENIC	homozygous	115352155
12	50394701	50394702	T	C	15	GENIC	homozygous	115352157
12	50395330	50395331	A	G	23	GENIC	homozygous	115352159
12	50396094	50396095	A	G	18	GENIC	homozygous	115403544
12	50397341	50397342	A	G	14	GENIC	homozygous	115352163
12	50397837	50397838	G	A	22	GENIC	homozygous	115352167
12	50398365	50398366	A	G	24	GENIC	homozygous	115352169
12	50398698	50398699	C	T	17	GENIC	homozygous	115403546
12	50398830	50398831	G	A	19	GENIC	homozygous	115403548
12	50399025	50399026	C	T	10	GENIC	homozygous	115352173
12	50399183	50399184	A	G	12	GENIC	homozygous	115352175
12	50399436	50399437	C	T	11	GENIC	homozygous	115352179
12	50399685	50399686	G	A	15	GENIC	homozygous	115352181
12	50400539	50400540	C	T	10	GENIC	homozygous	115403550
12	50400570	50400571	A	T	6	GENIC	homozygous	115352183
12	50400602	50400603	A	G	10	GENIC	homozygous	115352185
12	50401260	50401261	G	A	15	GENIC	homozygous	115352187
12	50401276	50401277	C	T	13	GENIC	homozygous	115352189
12	50401950	50401951	A	G	12	GENIC	homozygous	115352193
12	50402025	50402026	G	A	14	GENIC	homozygous	115352195
12	50403169	50403170	G	A	11	GENIC	homozygous	115403552
12	50403645	50403646	T	C	14	GENIC	homozygous	115352197
12	50404278	50404279	G	A	12	GENIC	homozygous	115352199
12	50404316	50404317	C	T	12	GENIC	homozygous	115352201
12	50404413	50404414	T	C	11	GENIC	homozygous	115352203