chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	59085000	59085001	A	G	31	GENIC	homozygous	51464960
10	59085254	59085255	C	T	13	GENIC	homozygous	51464961
10	59087456	59087457	T	C	23	GENIC	homozygous	51464962
10	59088133	59088134	A	G	34	GENIC	homozygous	51464963
10	59090119	59090120	T	TCA	13	GENIC	homozygous	51464965
10	59090122	59090123	T	TTTCAAAA	5	GENIC	homozygous	51464966
10	59091626	59091627	C	T	12	GENIC	homozygous	51464967
10	59091824	59091825	A	AAAAACAAAAC	7	GENIC	homozygous	51464968
10	59092718	59092719	T	TTGGA	6	GENIC	homozygous	51464969
10	59093116	59093117	A	G	20	GENIC	homozygous	51464970
10	59094039	59094040	A	G	25	GENIC	homozygous	51464971
10	59094163	59094164	T	TA	20	GENIC	homozygous	51464972
10	59094802	59094804	CT	--	19	GENIC	homozygous	51464973
10	59094873	59094874	G	A	23	GENIC	homozygous	51464974
10	59095091	59095092	C	T	27	GENIC	homozygous	51464975
10	59095092	59095093	A	G	27	GENIC	homozygous	51464976
10	59096110	59096111	G	A	8	GENIC	homozygous	51464977
10	59096652	59096653	T	TC	11	GENIC	homozygous	51464978
10	59096756	59096757	C	T	12	GENIC	homozygous	51464979
10	59097185	59097186	C	T	11	GENIC	homozygous	51464980
10	59098160	59098161	T	C	21	GENIC	homozygous	51464981
10	59098704	59098705	T	A	24	GENIC	homozygous	51464982