chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5902142	5902143	C	-	17	GENIC	homozygous	45390708
20	5902425	5902426	C	T	19	GENIC	homozygous	45390716
20	5902965	5902966	T	C	33	GENIC	homozygous	45390718
20	5903136	5903137	C	CTTTTT	12	GENIC	possibly homozygous	45839648
20	5903906	5903907	G	A	40	GENIC	homozygous	45390720
20	5903913	5903914	C	A	40	GENIC	homozygous	45390722
20	5903972	5903973	C	T	30	GENIC	homozygous	45390724
20	5904884	5904885	T	C	48	GENIC	homozygous	45390726
20	5904935	5904936	T	C	38	GENIC	homozygous	45390728
20	5905239	5905251	CCTGGGGTCACA	------------	23	GENIC	homozygous	45673055
20	5905266	5905267	A	G	29	GENIC	homozygous	45390730
20	5905347	5905348	G	A	33	GENIC	homozygous	45673056
20	5905425	5905426	C	T	50	GENIC	possibly homozygous	45390732
20	5905711	5905712	C	-	8	GENIC	heterozygous	45818607
20	5905924	5905925	C	G	18	GENIC	homozygous	45673057
20	5906031	5906032	G	T	23	GENIC	homozygous	45390736
20	5906043	5906044	A	G	23	GENIC	homozygous	45390738
20	5906107	5906108	A	C	20	GENIC	homozygous	45390740
20	5907095	5907096	T	A	26	GENIC	homozygous	45673058
20	5907521	5907522	T	C	30	GENIC	homozygous	45390742
20	5908141	5908144	AAG	---	20	GENIC	homozygous	45390745
20	5908414	5908415	G	-	14	GENIC	homozygous	45390747