chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	33261858	33261859	G	C	8	GENIC	homozygous	66724782
12	33261881	33261882	A	G	18	GENIC	homozygous	66724784
12	33261975	33261976	A		8	GENIC	homozygous	67337841
12	33262031	33262032	G	C	18	GENIC	homozygous	66724788
12	33262065	33262066	T	C	4	GENIC	homozygous	67574732
12	33262066	33262067	C	T	4	GENIC	homozygous	67574734
12	33262068	33262069	A	C	8	GENIC	homozygous	67437802
12	33262071	33262072	T	C	7	GENIC	homozygous	67437804
12	33262073	33262074	A	C	4	GENIC	homozygous	67574736
12	33262074	33262075	G	T	4	GENIC	homozygous	67574738
12	33262075	33262076	A	G	4	GENIC	homozygous	67574740
12	33262153	33262153		C	14	GENIC	homozygous	67574742
12	33262179	33262180	G		14	GENIC	homozygous	67337843
12	33262240	33262241	T	C	12	GENIC	homozygous	66724792
12	33262242	33262243	T	C	12	GENIC	homozygous	66724794
12	33262350	33262351	C	G	12	GENIC	homozygous	66724796
12	33270654	33270655	C	G	9	GENIC	homozygous	66724823