chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	89034266	89034267	C	G	22	GENIC	homozygous	51536515
10	89034268	89034269	C	A	22	GENIC	homozygous	51536516
10	89034756	89034757	A	G	37	GENIC	homozygous	52165279
10	89034800	89034801	C	A	34	GENIC	homozygous	52165280
10	89035266	89035267	G	T	10	GENIC	possibly homozygous	52165281
10	89035286	89035287	A	T	12	GENIC	possibly homozygous	52165282
10	89035496	89035497	G	GT	25	GENIC	homozygous	51731188
10	89035995	89035996	T	C	36	GENIC	homozygous	51731194
10	89036156	89036157	G	A	35	GENIC	homozygous	52165283
10	89036384	89036387	TTT	---	22	GENIC	homozygous	51731204
10	89037051	89037052	G	GT	3	GENIC	homozygous	51536517
10	89037199	89037200	A	G	43	GENIC	homozygous	51731210
10	89037292	89037293	T	C	30	GENIC	homozygous	52165284
10	89037347	89037348	C	A	31	GENIC	homozygous	52165285
10	89037493	89037494	A	AC	19	GENIC	heterozygous	52165286
10	89037494	89037495	A	C	23	GENIC	heterozygous	52165287
10	89037494	89037495	A	AAC	21	GENIC	heterozygous	52165288
10	89037737	89037738	A	T	32	GENIC	homozygous	51731214
10	89038008	89038009	T	C	30	GENIC	homozygous	51731216
10	89038215	89038216	G	A	38	GENIC	homozygous	52165289
10	89039596	89039597	T	C	31	GENIC	possibly homozygous	51731225
10	89039608	89039609	C	CTG	34	GENIC	homozygous	51731227
10	89039713	89039714	T	TC	21	GENIC	homozygous	51731229
10	89041158	89041159	A	G	46	GENIC	homozygous	51731237
10	89041350	89041351	C	T	28	GENIC	homozygous	52165290
10	89041468	89041469	A	G	27	GENIC	homozygous	52165291
10	89041623	89041624	A	G	28	GENIC	homozygous	51731251