chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	30038604	30038605	T	G	14	GENIC	homozygous	51387636
10	30040108	30040111	CTT	---	5	GENIC	heterozygous	51387637
10	30040282	30040283	C	T	22	GENIC	possibly homozygous	51387638
10	30041466	30041467	T	C	19	INTERGENIC	possibly homozygous	51387639
10	30041758	30041759	T	G	17	INTERGENIC	homozygous	51387640
10	30041909	30041910	C	CA	17	INTERGENIC	possibly homozygous	51387641
10	30042113	30042114	G	C	13	INTERGENIC	heterozygous	51387642
10	30042357	30042358	C	T	9	INTERGENIC	homozygous	51387643
10	30044095	30044096	G	A	4	INTERGENIC	homozygous	51387647
10	30044664	30044665	G	C	14	INTERGENIC	heterozygous	51387648
10	30044959	30044960	T	C	17	INTERGENIC	possibly homozygous	51387649
10	30045258	30045259	G	A	22	INTERGENIC	possibly homozygous	51387650
10	30045929	30045930	G	A	24	INTERGENIC	possibly homozygous	51387652
10	30047758	30047759	C	T	21	INTERGENIC	possibly homozygous	51387654
10	30048040	30048041	A	C	10	INTERGENIC	heterozygous	51387655
10	30048106	30048109	CTC	---	8	INTERGENIC	homozygous	51387656
10	30048202	30048203	T	C	8	INTERGENIC	homozygous	51387657
10	30048522	30048523	C	A	21	INTERGENIC	homozygous	51387658
10	30048661	30048662	A	G	20	INTERGENIC	possibly homozygous	51387659