chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	105246162	105246163	A	ATGTGTGTGTGTG	7	GENIC	heterozygous	62148307
1	105246163	105246165	TG	--	7	GENIC	possibly homozygous	60780742
1	105247380	105247381	A	G	13	GENIC	homozygous	61491817
1	105247469	105247470	A	C	15	GENIC	homozygous	61491818
1	105247573	105247574	G	A	20	GENIC	homozygous	61737449
1	105247870	105247871	T	C	20	GENIC	homozygous	61491819
1	105248153	105248154	C	T	14	GENIC	homozygous	61737451
1	105248173	105248174	G	-	17	GENIC	homozygous	61737453
1	105248437	105248438	G	A	8	GENIC	homozygous	61491820
1	105249139	105249140	T	C	26	GENIC	homozygous	61491821
1	105249647	105249648	C	-	18	GENIC	possibly homozygous	61491823
1	105250683	105250684	C	CGTGTGTGT	2	GENIC	homozygous	62148309
1	105255006	105255007	C	A	10	GENIC	homozygous	60780745
1	105255009	105255015	CCCCCC	------	10	GENIC	homozygous	62148311
1	105255014	105255015	C	CGGGGGG	10	GENIC	homozygous	62148313
1	105255434	105255435	T	A	25	GENIC	homozygous	61737457
1	105255928	105255929	C	CT	6	GENIC	heterozygous	61737459
1	105256868	105256872	CACA	----	3	GENIC	homozygous	60780746
1	105257365	105257366	G	-	14	GENIC	homozygous	60780749
1	105258515	105258516	T	C	14	GENIC	homozygous	61737461
1	105259279	105259280	T	C	13	GENIC	homozygous	61737463
1	105259584	105259585	A	G	28	GENIC	homozygous	61737465
1	105259760	105259761	G	A	20	GENIC	homozygous	61737467
1	105259837	105259838	C	G	20	GENIC	homozygous	60780750
1	105259856	105259857	C	A	22	GENIC	homozygous	60780751
1	105260236	105260237	A	C	17	GENIC	homozygous	61491829