chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	47470151	47470152	T	C	23	GENIC	homozygous	115397590
12	47470368	47470369	G	A	24	GENIC	homozygous	115344111
12	47470624	47470625	C	T	33	GENIC	homozygous	118272741
12	47470759	47470760	T	C	28	GENIC	homozygous	115344113
12	47470994	47470995	T	A	25	GENIC	homozygous	115344115
12	47471034	47471035	T	G	34	GENIC	homozygous	115344117
12	47471550	47471551	C	G	16	GENIC	heterozygous	115704642
12	47471680	47471681	C	G	25	GENIC	homozygous	115344119
12	47471743	47471744	T	C	26	GENIC	homozygous	115344121
12	47471753	47471754	A	G	28	GENIC	homozygous	115344123
12	47471935	47471936	G	A	45	GENIC	homozygous	115344125
12	47472298	47472299	A	G	30	GENIC	homozygous	115344127
12	47472602	47472603	C	A	20	GENIC	heterozygous	118338360
12	47472975	47472976	T	C	38	GENIC	homozygous	115344129
12	47473319	47473320	G	A	39	GENIC	homozygous	115397592
12	47473447	47473448	C	T	47	GENIC	homozygous	115344131
12	47474712	47474713	A	C	31	GENIC	homozygous	115344133
12	47475192	47475193	C	G	37	GENIC	possibly homozygous	115480609
12	47476080	47476081	T	G	33	GENIC	homozygous	115344135
12	47476228	47476229	A	G	29	GENIC	homozygous	115344137
12	47476292	47476293	G	A	29	GENIC	homozygous	115344139
12	47477691	47477692	A	C	34	GENIC	possibly homozygous	115344141
12	47478426	47478427	A	G	22	GENIC	homozygous	115452060
12	47478798	47478799	G	A	31	GENIC	homozygous	115344143
12	47479348	47479349	G	A	31	GENIC	homozygous	115344145
12	47480418	47480419	C	T	29	GENIC	homozygous	115344147
12	47480513	47480514	C	T	35	GENIC	homozygous	115344149
12	47481140	47481141	C	T	36	GENIC	homozygous	115397594
12	47481620	47481621	A	T	35	GENIC	homozygous	115344151
12	47481925	47481926	A	C	9	GENIC	homozygous	115344153
12	47482141	47482142	C	T	6	GENIC	homozygous	118272742
12	47482965	47482966	C	T	30	GENIC	homozygous	115344155