chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	58516136	58516137	A	C	7	GENIC	homozygous	54422733
6	58516274	58516275	C	T	63	GENIC	heterozygous	54422736
6	58516311	58516312	A	C	83	GENIC	heterozygous	54422739
6	58516889	58516890	T	TC	8	GENIC	homozygous	54422742
6	58517369	58517370	T	TG	22	GENIC	homozygous	54422745
6	58518264	58518265	T	-	28	GENIC	homozygous	54422748
6	58518573	58518574	T	TAA	8	GENIC	homozygous	54422751
6	58518588	58518589	C	-	17	GENIC	homozygous	54422754
6	58518869	58518870	A	T	45	GENIC	homozygous	54422757
6	58519962	58519963	C	T	21	GENIC	homozygous	54422760
6	58520149	58520165	TCTCTCTCTCTCTCTC	----------------	3	GENIC	heterozygous	54422763
6	58520204	58520205	C	G	18	GENIC	heterozygous	54422766
6	58520228	58520229	T	G	23	GENIC	heterozygous	54422769
6	58521859	58521860	C	CA	12	GENIC	homozygous	54422772
6	58522320	58522321	C	G	56	GENIC	homozygous	54422775
6	58523522	58523523	C	T	57	GENIC	homozygous	54422778
6	58524266	58524267	T	TTCAA	19	GENIC	homozygous	54422781
6	58524268	58524269	G	GC	14	GENIC	homozygous	54422784
6	58524269	58524270	T	TTCA	14	GENIC	homozygous	54422787
6	58525043	58525044	G	T	30	GENIC	possibly homozygous	54422790
6	58525046	58525047	G	A	29	GENIC	homozygous	54422793
6	58526279	58526280	T	A	49	GENIC	heterozygous	54422796
6	58526281	58526282	T	A	50	GENIC	possibly homozygous	54422799
6	58526969	58526970	T	C	19	GENIC	homozygous	54422802
6	58527200	58527201	C	T	27	GENIC	homozygous	54422805
6	58528608	58528609	T	TAAA	30	GENIC	homozygous	54422808
6	58528754	58528755	G	GA	19	GENIC	homozygous	54422811