chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5106274	5106275	T	C	28	GENIC	homozygous	109076856
20	5106543	5106544	T	C	38	GENIC	homozygous	109233832
20	5106590	5106591	C	T	35	GENIC	homozygous	109076858
20	5106778	5106779	T	G	28	GENIC	homozygous	109076860
20	5106854	5106855	G	A	34	GENIC	homozygous	109233833
20	5107063	5107064	G	A	38	GENIC	homozygous	109233834
20	5107075	5107076	A	G	41	GENIC	homozygous	109076862
20	5107143	5107144	T	C	46	GENIC	homozygous	109076864
20	5107158	5107159	G	T	49	GENIC	homozygous	109076866
20	5107364	5107365	A	G	36	GENIC	homozygous	109076867
20	5107368	5107369	T	C	35	GENIC	homozygous	109076869
20	5107372	5107373	C	T	34	GENIC	homozygous	109076871
20	5107540	5107541	T	C	32	GENIC	homozygous	109076873
20	5107676	5107677	G	A	24	GENIC	homozygous	109233835
20	5108126	5108127	A	C	43	GENIC	homozygous	109076875
20	5108383	5108384	A	T	29	GENIC	homozygous	109076877
20	5108384	5108385	G	A	29	GENIC	homozygous	109076879
20	5108435	5108436	C	T	22	GENIC	homozygous	109076881