chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	58116197	58116198	A	C	22	GENIC	homozygous	52658334
8	58116534	58116535	G	T	16	GENIC	homozygous	52982034
8	58116749	58116750	C	T	29	GENIC	homozygous	52982035
8	58117192	58117193	G	A	27	GENIC	homozygous	52982036
8	58117578	58117579	T	A	17	GENIC	homozygous	53699150
8	58117610	58117611	C	T	14	GENIC	homozygous	52982037
8	58117683	58117684	G	A	19	GENIC	homozygous	52982038
8	58117711	58117712	A	G	13	GENIC	homozygous	52982039
8	58117726	58117727	A	G	19	GENIC	homozygous	52658338
8	58118150	58118151	T	C	12	GENIC	homozygous	52982040
8	58118154	58118155	G	T	14	GENIC	homozygous	53699151
8	58118188	58118189	G	A	14	GENIC	homozygous	52982041
8	58118246	58118247	G	A	19	GENIC	homozygous	52982042
8	58118556	58118557	G	A	20	GENIC	homozygous	52982043
8	58118706	58118707	G	T	19	GENIC	homozygous	52982044
8	58119074	58119075	G	GT	21	GENIC	homozygous	52982045
8	58119235	58119236	A	ATGTTGTTGTTGTTGT	6	GENIC	homozygous	53699152
8	58119370	58119371	T	C	25	GENIC	homozygous	52658340
8	58119520	58119521	T	C	27	GENIC	homozygous	52982048
8	58119550	58119551	G	A	27	GENIC	homozygous	52982049
8	58119567	58119568	T	C	28	GENIC	homozygous	52982050
8	58119903	58119904	C	T	25	GENIC	homozygous	52658344
8	58120264	58120265	T	TCTC	23	GENIC	homozygous	52982051
8	58120637	58120638	T	G	27	GENIC	possibly homozygous	52982052
8	58120715	58120716	G	C	25	GENIC	homozygous	52982053
8	58121010	58121011	A	G	21	GENIC	homozygous	52982054
8	58121405	58121406	A	G	24	GENIC	homozygous	52982055