chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	35463493	35463494	G	A	38	GENIC	homozygous	51846747
10	35465325	35465330	GACAG	-----	18	GENIC	homozygous	51846750
10	35468353	35468356	CCG	---	9	GENIC	homozygous	51846753
10	35469068	35469069	G	GTTGTT	14	GENIC	homozygous	51846763
10	35471710	35471711	C	CA	25	GENIC	homozygous	51407720
10	35473249	35473250	G	A	22	GENIC	homozygous	51846781
10	35473359	35473360	G	A	21	GENIC	homozygous	51846784
10	35473617	35473619	AT	--	12	GENIC	possibly homozygous	52367454
10	35473706	35473707	T	TAA	17	GENIC	heterozygous	51846787
10	35473706	35473707	T	TA	17	GENIC	heterozygous	51846790
10	35474712	35474713	G	C	17	GENIC	homozygous	51846796
10	35469094	35469095	G	GT	7	GENIC	heterozygous	52435335
10	35469094	35469095	G	GTTTT	7	GENIC	heterozygous	52435337
10	35473637	35473638	A	ATG	10	GENIC	possibly homozygous	52435339
10	35471114	35471115	T	TA	17	GENIC	possibly homozygous	51634289
10	35471712	35471713	C	T	26	GENIC	homozygous	52316202
10	35473780	35473781	G	GGGGGGC	14	GENIC	homozygous	51846793