chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	32581905	32581906	C	-	27	GENIC	homozygous	50934550
12	32581956	32581957	A	-	38	GENIC	homozygous	50934553
12	32581958	32581959	G	T	38	GENIC	homozygous	50934556
12	32581959	32581960	G	GACAAAGCCTT	39	GENIC	homozygous	50934559
12	32581965	32581966	T	G	42	GENIC	homozygous	50934562
12	32581975	32581976	C	T	41	GENIC	homozygous	50934565
12	32581990	32581991	G	A	40	GENIC	homozygous	50934568
12	32581991	32581992	C	A	41	GENIC	homozygous	50934569
12	32582021	32582022	T	G	47	GENIC	homozygous	50934572
12	32582100	32582101	A	G	40	GENIC	homozygous	50934576
12	32582272	32582273	T	C	45	GENIC	homozygous	50934579
12	32582376	32582377	G	A	30	GENIC	homozygous	50934582
12	32582385	32582386	C	T	30	GENIC	homozygous	50934584
12	32582449	32582450	C	CA	23	GENIC	homozygous	50934587
12	32582477	32582478	A	C	26	GENIC	homozygous	50934590
12	32582491	32582492	T	C	31	GENIC	homozygous	50934593
12	32582571	32582572	T	C	36	GENIC	homozygous	50934596