chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	9892140	9892140		A	51	GENIC	homozygous	129657794
20	9892997	9892998	C	A	55	GENIC	homozygous	109089317
20	9893136	9893137	T	C	58	GENIC	homozygous	109089319
20	9893429	9893430	C	T	43	GENIC	homozygous	109237365
20	9892643	9892644	C	T	46	GENIC	homozygous	109237361
20	9892944	9892945	G	A	54	GENIC	homozygous	109237362
20	9893218	9893219	C	T	62	GENIC	homozygous	109237363
20	9893231	9893232	A	G	59	GENIC	homozygous	109237364
20	9894070	9894071	G	A	45	GENIC	homozygous	109237369
20	9893488	9893489	C	T	53	GENIC	homozygous	109237366
20	9893654	9893655	C	T	61	GENIC	homozygous	109301296
20	9893872	9893873	G	A	54	GENIC	homozygous	109237367
20	9893924	9893925	T	C	52	GENIC	homozygous	109237368
20	9894045	9894046	G	A	51	GENIC	homozygous	109089329
20	9894278	9894279	T	A	34	GENIC	homozygous	131560989
20	9894291	9894298	GGAGCTG		31	GENIC	homozygous	129657799
20	9895620	9895621	T	C	58	GENIC	homozygous	109089334
20	9895669	9895670	T	C	62	GENIC	homozygous	109089336
20	9895679	9895680	C	G	64	GENIC	homozygous	109089338
20	9894773	9894774	G		6	GENIC	heterozygous	131556141