chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	58115537	58115538	T	C	9	GENIC	possibly homozygous	52982030
8	58115551	58115555	ACTT	----	10	GENIC	homozygous	53121709
8	58115586	58115587	T	-	12	GENIC	homozygous	52982031
8	58115595	58115596	T	TC	15	GENIC	homozygous	52658330
8	58115651	58115652	A	C	15	GENIC	homozygous	52982032
8	58116197	58116198	A	C	13	GENIC	homozygous	52658334
8	58116534	58116535	G	T	27	GENIC	homozygous	52982034
8	58117192	58117193	G	A	20	GENIC	homozygous	52982036
8	58117647	58117648	A	C	20	GENIC	homozygous	53121711
8	58117683	58117684	G	A	16	GENIC	homozygous	52982038
8	58117711	58117712	A	G	16	GENIC	homozygous	52982039
8	58117726	58117727	A	G	17	GENIC	homozygous	52658338
8	58118150	58118151	T	C	34	GENIC	homozygous	52982040
8	58119235	58119236	A	ATGTTGTTGT	18	GENIC	homozygous	52982046
8	58119238	58119239	A	T	20	GENIC	homozygous	52982047
8	58119370	58119371	T	C	26	GENIC	homozygous	52658340
8	58119567	58119568	T	C	26	GENIC	homozygous	52982050
8	58119903	58119904	C	T	23	GENIC	homozygous	52658344
8	58120264	58120265	T	TCTC	29	GENIC	homozygous	52982051
8	58120675	58120676	C	T	23	GENIC	homozygous	53121712
8	58120715	58120716	G	C	22	GENIC	homozygous	52982053
8	58121010	58121011	A	G	20	GENIC	homozygous	52982054
8	58121405	58121406	A	G	9	GENIC	homozygous	52982055