chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	4066865	4066866	T	C	42	INTERGENIC	homozygous	45374743
20	4067292	4067293	A	-	28	INTERGENIC	homozygous	45374744
20	4067292	4067293	A	AT	30	INTERGENIC	homozygous	45374746
20	4067295	4067296	A	-	4	INTERGENIC	homozygous	45620610
20	4067315	4067316	A	-	22	INTERGENIC	homozygous	45374748
20	4067319	4067320	A	-	30	INTERGENIC	heterozygous	45374749
20	4067323	4067340	AAATAAATAAATAAATA	-----------------	22	INTERGENIC	homozygous	45374751
20	4067339	4067340	A	-	28	INTERGENIC	homozygous	45374752
20	4067353	4067354	G	T	34	INTERGENIC	homozygous	45374754
20	4067874	4067875	G	T	36	INTERGENIC	possibly homozygous	45374755
20	4067889	4067890	C	CT	13	INTERGENIC	homozygous	45374757
20	4068863	4068864	A	G	45	INTERGENIC	possibly homozygous	45374758
20	4068867	4068868	G	GA	38	INTERGENIC	homozygous	45374759
20	4068946	4068947	T	G	55	INTERGENIC	homozygous	45374761
20	4069835	4069840	TGTGT	-----	8	INTERGENIC	homozygous	45374762
20	4069837	4069840	TGT	---	8	INTERGENIC	homozygous	45374764
20	4070017	4070018	G	GA	4	INTERGENIC	heterozygous	45374765
20	4070028	4070029	A	-	10	INTERGENIC	heterozygous	45374767
20	4070181	4070182	T	TTGTA	22	INTERGENIC	homozygous	45374769