chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5902142	5902143	C	-	45	GENIC	homozygous	45390708
20	5902226	5902227	G	A	29	GENIC	possibly homozygous	45390710
20	5902264	5902265	C	CAT	11	GENIC	homozygous	45390712
20	5902271	5902284	GACCGCCTCCTCC	-------------	6	GENIC	homozygous	45390714
20	5902425	5902426	C	T	24	GENIC	possibly homozygous	45390716
20	5902965	5902966	T	C	50	GENIC	possibly homozygous	45390718
20	5903906	5903907	G	A	48	GENIC	homozygous	45390720
20	5903913	5903914	C	A	52	GENIC	homozygous	45390722
20	5903972	5903973	C	T	51	GENIC	homozygous	45390724
20	5904884	5904885	T	C	63	GENIC	possibly homozygous	45390726
20	5904935	5904936	T	C	70	GENIC	homozygous	45390728
20	5905266	5905267	A	G	58	GENIC	homozygous	45390730
20	5905425	5905426	C	T	58	GENIC	homozygous	45390732
20	5905710	5905711	T	TCTC	19	GENIC	possibly homozygous	45390734
20	5906031	5906032	G	T	43	GENIC	homozygous	45390736
20	5906043	5906044	A	G	49	GENIC	homozygous	45390738
20	5906107	5906108	A	C	53	GENIC	homozygous	45390740
20	5907521	5907522	T	C	51	GENIC	homozygous	45390742
20	5908141	5908144	AAG	---	45	GENIC	homozygous	45390745
20	5908414	5908415	G	-	37	GENIC	homozygous	45390747