chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	6956982	6956983	A	C	42	GENIC	homozygous	45406651
20	6957086	6957087	C	T	29	GENIC	homozygous	45406652
20	6957113	6957117	AAAA	----	25	GENIC	homozygous	45406653
20	6957507	6957508	C	CTT	22	GENIC	homozygous	45406654
20	6957562	6957563	G	A	53	GENIC	homozygous	45406655
20	6957622	6957623	A	T	48	GENIC	homozygous	45406656
20	6957711	6957712	A	G	44	GENIC	homozygous	45406657
20	6957713	6957714	G	C	42	GENIC	homozygous	45406658
20	6958140	6958141	C	G	40	GENIC	possibly homozygous	45406659
20	6960559	6960560	A	G	69	GENIC	homozygous	45406660
20	6960720	6960721	T	TG	16	GENIC	homozygous	45406661
20	6961054	6961055	G	GAAAAA	19	GENIC	heterozygous	45406662
20	6961054	6961055	G	GAAAAAA	19	GENIC	heterozygous	45406663
20	6961245	6961246	G	A	64	GENIC	homozygous	45406664
20	6961701	6961702	T	-	18	GENIC	homozygous	45406665
20	6961711	6961712	T	-	18	GENIC	possibly homozygous	45406666
20	6961730	6961731	G	GTTT	8	GENIC	homozygous	45406667
20	6961856	6961857	T	TA	38	GENIC	homozygous	45406668
20	6961931	6961935	AGAG	----	7	GENIC	homozygous	45406669
20	6961999	6962000	A	T	29	GENIC	homozygous	45406670