chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	59571205	59571206	C	T	35	GENIC	homozygous	51465805
10	59574227	59574232	AAACC	-----	17	GENIC	homozygous	51465813
10	59578489	59578490	A	AT	13	GENIC	heterozygous	51465817
10	59579048	59579049	C	-	25	GENIC	homozygous	51663665
10	59585105	59585106	G	A	24	GENIC	homozygous	51663669
10	59579050	59579051	T	A	25	GENIC	homozygous	52844660
10	59584422	59584440	GTGTGTGTGTGTGTGTGT	------------------	9	GENIC	homozygous	52844663
10	59587562	59587563	G	GCTGAAAGATCCCACGCAGAGAGAC	14	GENIC	possibly homozygous	53148652
10	59589267	59589268	C	-	25	GENIC	homozygous	51663671
10	59589501	59589502	C	A	26	GENIC	homozygous	51663673
10	59589767	59589768	T	C	31	GENIC	homozygous	51465835
10	59590505	59590506	G	A	17	GENIC	homozygous	51663675
10	59590585	59590586	G	A	33	GENIC	homozygous	51663677
10	59591293	59591300	GGCATTT	-------	48	GENIC	homozygous	51465836
10	59592896	59592897	C	A	31	GENIC	homozygous	51663683
10	59593075	59593076	C	A	36	GENIC	homozygous	51663685
10	59593907	59593908	T	C	36	GENIC	homozygous	51465837
10	59594683	59594684	A	AACACACAC	1	GENIC	homozygous	52379148
10	59595791	59595792	C	T	41	GENIC	homozygous	51663687
10	59596051	59596052	G	A	46	GENIC	homozygous	51663689
10	59596595	59596596	T	TAA	34	GENIC	homozygous	51663691
10	59596806	59596807	G	A	28	GENIC	homozygous	51663693
10	59596958	59596959	T	C	27	GENIC	homozygous	51663695
10	59597018	59597019	T	A	31	GENIC	homozygous	51663697
10	59597104	59597105	A	AG	15	GENIC	homozygous	51663699
10	59597417	59597418	C	T	26	GENIC	homozygous	51663703
10	59598261	59598262	T	TATC	30	GENIC	homozygous	51663705
10	59598873	59598874	A	T	27	GENIC	homozygous	51663707
10	59599284	59599285	G	T	35	GENIC	homozygous	51465839
10	59599484	59599485	C	T	24	GENIC	homozygous	51663709
10	59599899	59599900	G	A	30	GENIC	possibly homozygous	51663711
10	59600128	59600129	G	-	34	GENIC	homozygous	51465841