chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	10574921	10574922	T	A	34	GENIC	possibly homozygous	115415065
12	10574940	10574941	G	T	34	GENIC	possibly homozygous	118243892
12	10577766	10577767	G	T	29	GENIC	homozygous	115253888
12	10575142	10575143	T	G	24	GENIC	homozygous	115253880
12	10576473	10576474	T	A	21	GENIC	homozygous	115253882
12	10577263	10577264	G	T	22	GENIC	homozygous	115253886
12	10578165	10578166	A	G	55	GENIC	homozygous	115253890
12	10580544	10580545	T	C	27	GENIC	homozygous	115253892
12	10580682	10580683	T	C	34	GENIC	homozygous	115253894
12	10582526	10582527	T	C	51	GENIC	homozygous	115253896
12	10582772	10582773	C	T	56	GENIC	homozygous	115253898
12	10582983	10582984	A	G	19	GENIC	heterozygous	115253900