chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	106338269	106338270	A	T	2	GENIC	homozygous	51590538
10	106347075	106347077	CC	--	5	GENIC	heterozygous	51765377
10	106347090	106347091	C	CGTGT	3	GENIC	heterozygous	52447723
10	106347091	106347093	GT	--	3	GENIC	heterozygous	52447725
10	106347122	106347123	T	TGTGC	6	GENIC	heterozygous	52406998
10	106348795	106348797	TT	--	18	GENIC	heterozygous	52447727
10	106348796	106348797	T	-	18	GENIC	heterozygous	52407000
10	106354189	106354190	T	C	17	GENIC	possibly homozygous	51590543
10	106362564	106362565	G	GTTT	14	GENIC	homozygous	51590545
10	106362572	106362573	G	GT	6	GENIC	heterozygous	52447729
10	106368841	106368842	T	TG	4	GENIC	homozygous	51590551
10	106374268	106374269	C	-	1	GENIC	homozygous	51590559
10	106384747	106384748	A	ATG	3	GENIC	homozygous	52407076
10	106384750	106384751	T	TGCTAGGCAAGCGCTCTACCACTGAGCTAAA	3	GENIC	homozygous	52407078
10	106384755	106384757	GG	--	4	GENIC	homozygous	52447731
10	106384758	106384759	G	-	4	GENIC	homozygous	51590577
10	106393629	106393630	T	-	11	GENIC	possibly homozygous	52447733
10	106402252	106402253	G	GA	13	GENIC	homozygous	51590581