chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	13340354	13340355	C	CGTGT	17	GENIC	possibly homozygous	45687540
20	13343283	13343284	C	CT	13	GENIC	heterozygous	45432877
20	13343283	13343284	C	CTT	13	GENIC	heterozygous	45432878
20	13348905	13348906	T	TC	9	GENIC	heterozygous	45432890
20	13348906	13348907	C	-	9	GENIC	heterozygous	45432891
20	13350302	13350303	T	C	20	GENIC	possibly homozygous	45432896
20	13357483	13357484	A	AC	7	GENIC	heterozygous	45432908
20	13358156	13358157	A	G	14	GENIC	homozygous	45432909
20	13360854	13360855	A	T	17	GENIC	possibly homozygous	45622983
20	13361209	13361210	A	-	29	GENIC	homozygous	45687541
20	13363057	13363058	C	G	32	GENIC	homozygous	45432915
20	13363082	13363083	A	G	35	GENIC	heterozygous	45432918
20	13363753	13363754	G	GT	36	GENIC	heterozygous	45432921
20	13363960	13363961	G	GC	45	GENIC	heterozygous	45432926
20	13363963	13363964	A	T	53	GENIC	heterozygous	45432927
20	13364016	13364017	T	G	44	GENIC	heterozygous	45432928
20	13364033	13364034	A	G	36	GENIC	heterozygous	45432930
20	13364071	13364072	A	AGT	18	GENIC	heterozygous	45622985
20	13364101	13364102	T	-	15	GENIC	heterozygous	45738920
20	13363672	13363673	T	G	81	GENIC	heterozygous	45738917
20	13363754	13363755	G	C	58	GENIC	heterozygous	45738918
20	13363755	13363756	A	T	57	GENIC	heterozygous	45738919
20	13364120	13364121	G	-	7	GENIC	heterozygous	45432932
20	13364125	13364126	A	AGCT	11	GENIC	possibly homozygous	45432933
20	13370918	13370919	T	C	31	GENIC	possibly homozygous	45432942
20	13373158	13373159	G	GT	19	GENIC	heterozygous	45432947
20	13374807	13374808	C	CA	5	GENIC	heterozygous	45622986
20	13377436	13377437	G	T	22	GENIC	heterozygous	45432960
20	13378101	13378102	C	CG	24	GENIC	homozygous	45687543
20	13378878	13378880	GT	--	19	GENIC	heterozygous	45687544