chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	9892140	9892140		A	36	GENIC	homozygous	129657794
20	9892997	9892998	C	A	48	GENIC	homozygous	109089317
20	9893136	9893137	T	C	58	GENIC	homozygous	109089319
20	9892643	9892644	C	T	52	GENIC	homozygous	109237361
20	9892944	9892945	G	A	38	GENIC	homozygous	109237362
20	9893218	9893219	C	T	42	GENIC	homozygous	109237363
20	9893231	9893232	A	G	36	GENIC	homozygous	109237364
20	9892878	9892879	C	G	43	GENIC	homozygous	109301292
20	9893189	9893190	C	T	46	GENIC	homozygous	109301294
20	9893639	9893640	C		40	GENIC	homozygous	129657797
20	9893654	9893655	C	T	41	GENIC	homozygous	109301296
20	9893667	9893668	T	C	45	GENIC	homozygous	109089323
20	9893707	9893707		CTGGCACT	36	GENIC	homozygous	129657798
20	9895620	9895621	T	C	37	GENIC	homozygous	109089334
20	9895669	9895670	T	C	42	GENIC	homozygous	109089336
20	9895679	9895680	C	G	44	GENIC	homozygous	109089338
20	9893670	9893671	A		46	GENIC	homozygous	131229148
20	9894778	9894779	A		12	GENIC	possibly homozygous	131229149