chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	23657087	23657088	C	G	7	GENIC	homozygous	115285372
12	23657139	23657140	C	T	12	GENIC	homozygous	115285374
12	23657259	23657260	C	T	14	GENIC	homozygous	115285376
12	23657289	23657290	C	T	16	GENIC	homozygous	115285378
12	23657298	23657299	T	C	16	GENIC	homozygous	115285380
12	23657448	23657449	T	C	3	GENIC	homozygous	115285382
12	23657565	23657566	T	C	19	GENIC	homozygous	115285384
12	23657567	23657568	A	G	18	GENIC	homozygous	115285386
12	23657603	23657604	A	C	12	GENIC	homozygous	115285388
12	23657605	23657606	G	T	13	GENIC	homozygous	115285390
12	23658079	23658080	G	A	22	GENIC	homozygous	115368505
12	23658194	23658195	T	C	9	GENIC	homozygous	115285406
12	23658260	23658261	C	T	17	GENIC	homozygous	115285408
12	23658313	23658314	G	A	6	GENIC	homozygous	115285410
12	23658388	23658389	G	A	14	GENIC	homozygous	115285412
12	23658572	23658573	T	C	11	GENIC	homozygous	115285414
12	23658573	23658574	G	A	11	GENIC	homozygous	115285416
12	23658626	23658627	G	T	6	GENIC	homozygous	115285418
12	23658783	23658784	G	A	9	GENIC	homozygous	115285420
12	23659497	23659498	A	C	27	GENIC	homozygous	115285422
12	23659673	23659674	C	T	19	GENIC	homozygous	115285424
12	23660709	23660710	C	T	21	GENIC	homozygous	115285426
12	23660739	23660740	G	A	19	GENIC	homozygous	115285428