chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	24566643	24566644	C	T	53	GENIC	homozygous	115288357
12	24566689	24566690	G	A	50	GENIC	homozygous	115288359
12	24569115	24569116	G	A	51	GENIC	possibly homozygous	115288361
12	24569473	24569474	A	G	57	GENIC	homozygous	115446922
12	24569535	24569536	C	T	69	GENIC	homozygous	115288363
12	24570045	24570046	T	C	44	GENIC	homozygous	118262140
12	24570529	24570530	T	C	32	GENIC	homozygous	115288365
12	24571946	24571947	A	G	57	GENIC	homozygous	115288367
12	24572529	24572530	C	T	68	GENIC	homozygous	115288369
12	24573197	24573198	T	C	56	GENIC	homozygous	115288371
12	24574267	24574268	T	C	52	GENIC	homozygous	115288373
12	24574793	24574794	T	G	51	GENIC	homozygous	115288375
12	24574974	24574975	T	G	49	GENIC	homozygous	115288377
12	24575915	24575916	G	A	60	GENIC	homozygous	115288379
12	24576191	24576192	G	A	17	GENIC	homozygous	118262141
12	24576466	24576467	C	T	34	GENIC	homozygous	115288381
12	24576630	24576631	G	A	28	GENIC	homozygous	115288383
12	24577339	24577340	C	T	45	GENIC	homozygous	118262142
12	24577761	24577762	T	C	49	GENIC	homozygous	115288385
12	24578363	24578364	T	C	44	GENIC	homozygous	115288387