chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	47470151	47470152	T	C	7	GENIC	homozygous	115397590
12	47470368	47470369	G	A	8	GENIC	homozygous	115344111
12	47470759	47470760	T	C	5	GENIC	homozygous	115344113
12	47470994	47470995	T	A	10	GENIC	homozygous	115344115
12	47471034	47471035	T	G	7	GENIC	homozygous	115344117
12	47471680	47471681	C	G	10	GENIC	homozygous	115344119
12	47471743	47471744	T	C	5	GENIC	homozygous	115344121
12	47471753	47471754	A	G	5	GENIC	homozygous	115344123
12	47471935	47471936	G	A	4	GENIC	homozygous	115344125
12	47472975	47472976	T	C	16	GENIC	homozygous	115344129
12	47473319	47473320	G	A	8	GENIC	homozygous	115397592
12	47473447	47473448	C	T	7	GENIC	homozygous	115344131
12	47476080	47476081	T	G	5	GENIC	homozygous	115344135
12	47477691	47477692	A	C	19	GENIC	homozygous	115344141
12	47478798	47478799	G	A	5	GENIC	homozygous	115344143
12	47479348	47479349	G	A	7	GENIC	homozygous	115344145
12	47480513	47480514	C	T	9	GENIC	homozygous	115344149
12	47481140	47481141	C	T	6	GENIC	homozygous	115397594
12	47481620	47481621	A	T	4	GENIC	homozygous	115344151
12	47482965	47482966	C	T	8	GENIC	homozygous	115344155