chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5106261	5106262	G	A	44	GENIC	homozygous	109076854
20	5106274	5106275	T	C	43	GENIC	homozygous	109076856
20	5106543	5106544	T	C	27	GENIC	homozygous	109233832
20	5106778	5106779	T	A	31	GENIC	homozygous	109455499
20	5107063	5107064	G	A	35	GENIC	homozygous	109233834
20	5107075	5107076	A	G	35	GENIC	homozygous	109076862
20	5107143	5107144	T	C	33	GENIC	homozygous	109076864
20	5107158	5107159	G	T	36	GENIC	homozygous	109076866
20	5107364	5107365	A	G	40	GENIC	homozygous	109076867
20	5107368	5107369	T	C	40	GENIC	homozygous	109076869
20	5107378	5107379	T	A	41	GENIC	homozygous	109455501
20	5107676	5107677	G	A	47	GENIC	homozygous	109233835
20	5108126	5108127	A	C	39	GENIC	homozygous	109076875
20	5108435	5108436	C	T	30	GENIC	homozygous	109076881