chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	59087415	59087416	C	T	34	GENIC	homozygous	51662587
10	59087456	59087457	T	C	23	GENIC	homozygous	51464962
10	59089948	59089949	A	-	12	GENIC	homozygous	51464964
10	59090119	59090120	T	TCA	19	GENIC	homozygous	51464965
10	59090120	59090121	G	T	19	GENIC	homozygous	52319538
10	59090122	59090123	T	TTTCAAAA	20	GENIC	homozygous	51464966
10	59090124	59090125	C	A	20	GENIC	homozygous	52248798
10	59091626	59091627	C	T	34	GENIC	homozygous	51464967
10	59091824	59091825	A	AAAAACAAAAC	20	GENIC	homozygous	51464968
10	59093116	59093117	A	G	38	GENIC	homozygous	51464970
10	59094039	59094040	A	G	30	GENIC	homozygous	51464971
10	59094153	59094154	G	A	27	GENIC	homozygous	51662591
10	59094163	59094164	T	TA	29	GENIC	homozygous	51464972
10	59094873	59094874	G	A	38	GENIC	homozygous	51464974
10	59095091	59095092	C	T	37	GENIC	homozygous	51464975
10	59095092	59095093	A	G	38	GENIC	homozygous	51464976
10	59096075	59096076	C	CAAAAAAA	26	GENIC	homozygous	52378903
10	59096110	59096111	G	A	26	GENIC	homozygous	51464977
10	59096756	59096757	C	T	32	GENIC	homozygous	51464979
10	59097115	59097116	A	G	27	GENIC	homozygous	51662593
10	59098704	59098705	T	A	33	GENIC	possibly homozygous	51464982
10	59099033	59099034	A	AGGC	1	GENIC	homozygous	51662595