chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3428247	3428248	T	C	42	GENIC	homozygous	109068770
20	3428459	3428460	A	T	35	GENIC	homozygous	109068772
20	3428545	3428546	G	T	25	GENIC	homozygous	109068774
20	3428831	3428832	C	T	30	GENIC	homozygous	109068776
20	3429098	3429099	T	C	33	GENIC	homozygous	109068778
20	3429467	3429468	G	T	40	GENIC	homozygous	109068780
20	3430341	3430342	T	A	45	GENIC	homozygous	109068782
20	3430484	3430485	G	A	65	GENIC	homozygous	109068784
20	3430790	3430791	C	A	35	GENIC	homozygous	109068786
20	3431525	3431526	T	A	38	GENIC	homozygous	109068788
20	3432038	3432039	T	C	50	GENIC	homozygous	109068790
20	3432739	3432740	G	C	50	GENIC	possibly homozygous	109068792
20	3433017	3433018	T	C	40	GENIC	homozygous	109068794
20	3433344	3433345	T	C	30	GENIC	homozygous	109068796
20	3434803	3434804	C	T	35	GENIC	homozygous	109068798
20	3435091	3435092	T	C	46	GENIC	homozygous	109068800
20	3435808	3435809	A	G	37	GENIC	homozygous	109068802
20	3435873	3435874	T	C	46	GENIC	homozygous	109068804
20	3436760	3436761	A	G	42	GENIC	homozygous	109068806
20	3437818	3437819	A	G	19	GENIC	homozygous	109068808
20	3437963	3437964	A	C	29	GENIC	homozygous	109068810
20	3437967	3437968	A	G	26	GENIC	homozygous	109068812
20	3438105	3438106	G	C	28	GENIC	homozygous	109068814
20	3438116	3438117	A	C	25	GENIC	homozygous	109068816
20	3438308	3438309	A	G	29	GENIC	homozygous	109068818