chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	35463493	35463494	G	A	26	GENIC	homozygous	51846747
10	35465325	35465330	GACAG	-----	12	GENIC	homozygous	51846750
10	35469715	35469716	T	C	18	GENIC	homozygous	52137715
10	35466194	35466195	G	A	20	GENIC	homozygous	52137709
10	35466402	35466403	G	A	6	GENIC	homozygous	52137711
10	35467519	35467520	C	G	18	GENIC	homozygous	52137713
10	35467938	35467941	CCG	---	2	GENIC	homozygous	52435333
10	35469094	35469095	G	GTTTT	7	GENIC	homozygous	52435337
10	35469068	35469069	G	GTTGT	14	GENIC	homozygous	53024673
10	35471114	35471115	T	TAA	13	GENIC	homozygous	52137717
10	35471494	35471495	G	A	28	GENIC	homozygous	52137719
10	35471710	35471711	C	CA	20	GENIC	homozygous	51407720
10	35473637	35473638	A	ATGTGTGTGTG	6	GENIC	homozygous	52647445
10	35473706	35473707	T	TAA	9	GENIC	homozygous	51846787
10	35473780	35473781	G	GGGGGGC	12	GENIC	homozygous	51846793
10	35471712	35471713	C	T	22	GENIC	possibly homozygous	52316202