chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	47470151	47470152	T	C	49	GENIC	homozygous	115397590
12	47470368	47470369	G	A	61	GENIC	possibly homozygous	115344111
12	47470759	47470760	T	C	41	GENIC	homozygous	115344113
12	47470994	47470995	T	A	67	GENIC	homozygous	115344115
12	47471034	47471035	T	G	59	GENIC	homozygous	115344117
12	47471680	47471681	C	G	36	GENIC	homozygous	115344119
12	47471743	47471744	T	C	35	GENIC	homozygous	115344121
12	47471753	47471754	A	G	40	GENIC	homozygous	115344123
12	47471935	47471936	G	A	37	GENIC	homozygous	115344125
12	47472298	47472299	A	G	46	GENIC	homozygous	115344127
12	47472975	47472976	T	C	63	GENIC	homozygous	115344129
12	47473319	47473320	G	A	36	GENIC	homozygous	115397592
12	47473447	47473448	C	T	51	GENIC	homozygous	115344131
12	47474712	47474713	A	C	9	GENIC	homozygous	115344133
12	47476080	47476081	T	G	40	GENIC	homozygous	115344135
12	47476228	47476229	A	G	20	GENIC	homozygous	115344137
12	47476292	47476293	G	A	26	GENIC	homozygous	115344139
12	47470624	47470625	C	T	41	GENIC	homozygous	118272741
12	47471550	47471551	C	G	22	GENIC	heterozygous	115704642
12	47475192	47475193	C	G	45	GENIC	homozygous	115480609
12	47477691	47477692	A	C	33	GENIC	homozygous	115344141
12	47478426	47478427	A	G	23	GENIC	homozygous	115452060
12	47478798	47478799	G	A	51	GENIC	homozygous	115344143
12	47479348	47479349	G	A	41	GENIC	possibly homozygous	115344145
12	47480418	47480419	C	T	42	GENIC	homozygous	115344147
12	47480513	47480514	C	T	48	GENIC	homozygous	115344149
12	47481140	47481141	C	T	40	GENIC	homozygous	115397594
12	47481620	47481621	A	T	23	GENIC	homozygous	115344151
12	47481925	47481926	A	C	25	GENIC	homozygous	115344153
12	47482141	47482142	C	T	12	GENIC	homozygous	118272742
12	47482156	47482157	G	T	28	GENIC	heterozygous	118272743
12	47482160	47482161	C	T	28	GENIC	heterozygous	118272744
12	47482965	47482966	C	T	63	GENIC	homozygous	115344155