chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5106261	5106262	G	A	40	GENIC	homozygous	109076854
20	5106274	5106275	T	C	45	GENIC	homozygous	109076856
20	5106543	5106544	T	C	53	GENIC	homozygous	109233832
20	5106590	5106591	C	T	52	GENIC	homozygous	109076858
20	5106778	5106779	T	G	48	GENIC	homozygous	109076860
20	5107063	5107064	G	A	61	GENIC	homozygous	109233834
20	5107075	5107076	A	G	56	GENIC	homozygous	109076862
20	5107143	5107144	T	C	50	GENIC	homozygous	109076864
20	5107158	5107159	G	T	54	GENIC	homozygous	109076866
20	5107364	5107365	A	G	62	GENIC	homozygous	109076867
20	5107368	5107369	T	C	62	GENIC	homozygous	109076869
20	5107372	5107373	C	T	61	GENIC	homozygous	109076871
20	5107540	5107541	T	C	48	GENIC	homozygous	109076873
20	5107676	5107677	G	A	55	GENIC	homozygous	109233835
20	5108126	5108127	A	C	47	GENIC	homozygous	109076875
20	5108435	5108436	C	T	58	GENIC	possibly homozygous	109076881