chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	10617082	10617083	A	G	12	GENIC	possibly homozygous	130052772
20	10617203	10617204	A	G	33	GENIC	homozygous	130052773
20	10617337	10617345	GAAAGAAG		29	GENIC	homozygous	140484832
20	10620738	10620739	G	A	44	GENIC	homozygous	130052774
20	10623317	10623318	A	C	42	GENIC	homozygous	140515307
20	10620202	10620203	G	A	46	GENIC	homozygous	140515304
20	10620921	10620922	A	G	56	GENIC	homozygous	140515305
20	10620954	10620955	C	T	52	GENIC	homozygous	140515306
20	10623878	10623879	G	A	55	GENIC	homozygous	130052779
20	10626831	10626832	T	C	27	GENIC	homozygous	130052785
20	10627778	10627779	T	A	49	GENIC	homozygous	130052786
20	10628708	10628709	T	C	48	GENIC	homozygous	130052787
20	10626433	10626437	TGTG		8	GENIC	heterozygous	145084380
20	10624064	10624065	G	A	40	GENIC	homozygous	142726257
20	10626819	10626820	G	A	25	GENIC	homozygous	142726258