chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	23655970	23655971	G	A	22	GENIC	homozygous	115560659
12	23657039	23657040	T	A	37	GENIC	homozygous	115285370
12	23657087	23657088	C	G	36	GENIC	homozygous	115285372
12	23657139	23657140	C	T	39	GENIC	homozygous	115285374
12	23657259	23657260	C	T	26	GENIC	homozygous	115285376
12	23657289	23657290	C	T	23	GENIC	homozygous	115285378
12	23657298	23657299	T	C	22	GENIC	homozygous	115285380
12	23658000	23658001	G	A	26	GENIC	homozygous	115560661
12	23658481	23658482	C	T	32	GENIC	homozygous	115560663
12	23658685	23658686	C	T	37	GENIC	homozygous	115560665
12	23659474	23659475	G	A	40	GENIC	possibly homozygous	115560667
12	23659801	23659802	A	C	43	GENIC	possibly homozygous	115560669
12	23659044	23659045	T	C	27	GENIC	possibly homozygous	115598174