chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	9892140	9892140		A	15	GENIC	homozygous	129657794
20	9892171	9892172	T	C	15	GENIC	homozygous	109089297
20	9892172	9892173	G	A	15	GENIC	homozygous	109089299
20	9892418	9892419	G	A	15	GENIC	homozygous	109089301
20	9892486	9892487	A		22	GENIC	homozygous	129657795
20	9892487	9892488	C	G	22	GENIC	homozygous	109089303
20	9892534	9892535	A	G	16	GENIC	homozygous	109089305
20	9892535	9892536	C	T	16	GENIC	homozygous	109089307
20	9892687	9892688	G	A	27	GENIC	homozygous	109089309
20	9892691	9892692	C	T	26	GENIC	homozygous	109089311
20	9892742	9892753	CTTGGTGGTCT		30	GENIC	homozygous	129657796
20	9892889	9892890	A	G	16	GENIC	homozygous	109089313
20	9892894	9892895	A	G	15	GENIC	homozygous	109089315
20	9892997	9892998	C	A	17	GENIC	homozygous	109089317
20	9893136	9893137	T	C	19	GENIC	homozygous	109089319
20	9892429	9892430	A	G	16	GENIC	homozygous	109421401
20	9892604	9892605	C	T	18	GENIC	homozygous	119767820
20	9892670	9892671	C	A	27	GENIC	homozygous	119767821
20	9892643	9892644	C	T	20	GENIC	homozygous	109237361
20	9892665	9892666	C	T	26	GENIC	homozygous	129708385
20	9892666	9892667	T	G	26	GENIC	homozygous	129708386
20	9893430	9893431	G	T	16	GENIC	homozygous	109089321
20	9893639	9893640	C		14	GENIC	homozygous	129657797
20	9893667	9893668	T	C	16	GENIC	homozygous	109089323
20	9893707	9893707		CTGGCACT	16	GENIC	homozygous	129657798
20	9893960	9893961	T	C	17	GENIC	homozygous	109089325
20	9894026	9894027	A	G	11	GENIC	homozygous	109089327
20	9894045	9894046	G	A	11	GENIC	homozygous	109089329
20	9894087	9894088	C	G	10	GENIC	homozygous	109089331
20	9894291	9894298	GGAGCTG		10	GENIC	homozygous	129657799
20	9895620	9895621	T	C	25	GENIC	homozygous	109089334
20	9895669	9895670	T	C	27	GENIC	homozygous	109089336
20	9895679	9895680	C	G	29	GENIC	homozygous	109089338