chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	10616992	10616993	G		12	GENIC	heterozygous	403464132
20	10616992	10616993	G	A	12	GENIC	heterozygous	403464133
20	10617082	10617083	A	G	16	GENIC	homozygous	130052772
20	10617203	10617204	A	G	27	GENIC	homozygous	130052773
20	10617337	10617345	GAAAGAAG		30	GENIC	homozygous	140484832
20	10620738	10620739	G	A	53	GENIC	homozygous	130052774
20	10623878	10623879	G	A	48	GENIC	homozygous	130052779
20	10623941	10623942	C	A	60	GENIC	homozygous	155136199
20	10620202	10620203	G	A	41	GENIC	homozygous	140515304
20	10620921	10620922	A	G	38	GENIC	homozygous	140515305
20	10620954	10620955	C	T	31	GENIC	homozygous	140515306
20	10623317	10623318	A	C	48	GENIC	homozygous	140515307
20	10626831	10626832	T	C	44	GENIC	homozygous	130052785
20	10627778	10627779	T	A	64	GENIC	possibly homozygous	130052786
20	10628708	10628709	T	C	63	GENIC	homozygous	130052787
20	10626433	10626437	TGTG		13	GENIC	heterozygous	145084380
20	10623941	10623942	C	T	60	GENIC	heterozygous	155136200
20	10624064	10624065	G	A	55	GENIC	homozygous	142726257
20	10626819	10626820	G	A	44	GENIC	homozygous	142726258