chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	10616992	10616993	G		13	GENIC	homozygous	403464132
20	10616992	10616993	G	A	13	GENIC	heterozygous	403464133
20	10617082	10617083	A	G	19	GENIC	homozygous	130052772
20	10617203	10617204	A	G	37	GENIC	homozygous	130052773
20	10617337	10617345	GAAAGAAG		31	GENIC	homozygous	140484832
20	10620738	10620739	G	A	58	GENIC	homozygous	130052774
20	10623878	10623879	G	A	46	GENIC	homozygous	130052779
20	10623941	10623942	C	A	61	GENIC	possibly homozygous	155136199
20	10623941	10623942	C	T	61	GENIC	heterozygous	155136200
20	10626831	10626832	T	C	44	GENIC	homozygous	130052785
20	10627778	10627779	T	A	46	GENIC	homozygous	130052786
20	10628708	10628709	T	C	55	GENIC	homozygous	130052787
20	10623317	10623318	A	C	49	GENIC	homozygous	140515307
20	10620202	10620203	G	A	49	GENIC	homozygous	140515304
20	10620921	10620922	A	G	51	GENIC	possibly homozygous	140515305
20	10620954	10620955	C	T	46	GENIC	possibly homozygous	140515306