chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	30038068	30038075	TTTTTTT	-------	13	GENIC	homozygous	51387635
10	30038604	30038605	T	G	21	GENIC	homozygous	51387636
10	30040108	30040111	CTT	---	23	GENIC	homozygous	51387637
10	30040282	30040283	C	T	32	GENIC	homozygous	51387638
10	30041466	30041467	T	C	43	INTERGENIC	homozygous	51387639
10	30041758	30041759	T	G	20	INTERGENIC	homozygous	51387640
10	30041909	30041910	C	CA	24	INTERGENIC	homozygous	51387641
10	30042113	30042114	G	C	26	INTERGENIC	homozygous	51387642
10	30042357	30042358	C	T	32	INTERGENIC	homozygous	51387643
10	30043007	30043015	GTGTGTGC	--------	24	INTERGENIC	possibly homozygous	51387645
10	30044095	30044096	G	A	20	INTERGENIC	homozygous	51387647
10	30044650	30044651	G	A	18	INTERGENIC	homozygous	52135484
10	30044664	30044665	G	C	15	INTERGENIC	homozygous	51387648
10	30044959	30044960	T	C	16	INTERGENIC	homozygous	51387649
10	30045258	30045259	G	A	17	INTERGENIC	homozygous	51387650
10	30045578	30045579	C	CCAA	5	INTERGENIC	homozygous	52135486
10	30045929	30045930	G	A	28	INTERGENIC	homozygous	51387652
10	30046910	30046916	TGTGTG	------	7	INTERGENIC	possibly homozygous	52135488
10	30047758	30047759	C	T	14	INTERGENIC	homozygous	51387654
10	30048040	30048041	A	C	14	INTERGENIC	homozygous	51387655
10	30048106	30048109	CTC	---	13	INTERGENIC	homozygous	51387656
10	30048202	30048203	T	C	13	INTERGENIC	homozygous	51387657
10	30048522	30048523	C	A	21	INTERGENIC	homozygous	51387658
10	30048661	30048662	A	G	30	INTERGENIC	homozygous	51387659