chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	105760024	105760025	T	C	20	GENIC	homozygous	49976659
13	105760417	105760418	T	C	13	GENIC	homozygous	49976660
13	105761149	105761150	G	A	9	GENIC	homozygous	49976661
13	105764979	105764980	T	G	19	GENIC	homozygous	49976667
13	105767280	105767281	T	A	17	GENIC	homozygous	49873882
13	105767282	105767283	T	C	17	GENIC	homozygous	49873883
13	105767541	105767543	GT	--	11	GENIC	homozygous	49976668
13	105768857	105768858	T	TGTCACAGCGGCGTCACGGGG	14	GENIC	homozygous	50597873
13	105769147	105769148	T	TC	10	GENIC	homozygous	49976670
13	105769165	105769166	C	CA	12	GENIC	homozygous	49976671
13	105769169	105769170	C	T	12	GENIC	homozygous	49976672
13	105770143	105770144	C	T	14	GENIC	homozygous	49976684
13	105770947	105770948	G	A	12	GENIC	homozygous	49976685
13	105771043	105771044	C	G	8	GENIC	homozygous	49976686
13	105771383	105771384	A	C	14	GENIC	homozygous	49976687
13	105771550	105771551	C	T	16	GENIC	homozygous	49976688
13	105774338	105774339	A	C	13	GENIC	homozygous	49976689
13	105776006	105776007	C	T	34	GENIC	homozygous	49976690
13	105776190	105776191	T	C	18	GENIC	homozygous	49976691
13	105776328	105776329	A	G	27	GENIC	homozygous	49976692
13	105769299	105769300	T	-	10	GENIC	homozygous	51257271
13	105769301	105769309	ATCATCAT	--------	10	GENIC	homozygous	51257273
13	105785531	105785532	C	T	20	GENIC	homozygous	49976694
13	105785887	105785888	A	G	21	GENIC	possibly homozygous	49976695
13	105788585	105788586	T	-	16	GENIC	homozygous	49976696
13	105790610	105790611	G	A	14	GENIC	homozygous	49976702
13	105793358	105793359	A	G	26	GENIC	homozygous	49976703
13	105794181	105794182	C	T	12	GENIC	homozygous	49976704
13	105806546	105806547	T	C	9	GENIC	homozygous	49976724
13	105806678	105806679	T	C	8	GENIC	homozygous	49976725
13	105807083	105807084	C	T	15	GENIC	homozygous	49976726
13	105807804	105807805	G	GAGAGAGAGAA	20	GENIC	homozygous	50813631