chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	139135363	139135364	T	C	17	GENIC	possibly homozygous	54145793
7	139139326	139139327	T	A	8	GENIC	heterozygous	54145805
7	139139487	139139488	T	C	17	GENIC	homozygous	54145807
7	139139761	139139762	C	T	10	GENIC	heterozygous	54145809
7	139139846	139139847	T	C	7	GENIC	possibly homozygous	54145811
7	139140112	139140113	A	G	17	GENIC	possibly homozygous	54145813
7	139140154	139140155	A	G	12	GENIC	heterozygous	54145815
7	139140373	139140374	A	G	19	GENIC	possibly homozygous	54145817
7	139141184	139141185	T	C	23	GENIC	heterozygous	54145819
7	139141224	139141226	TC	--	17	GENIC	homozygous	54145821
7	139141440	139141441	G	GT	2	GENIC	heterozygous	54258041
7	139141563	139141564	G	A	15	GENIC	possibly homozygous	54145823
7	139142509	139142510	A	G	2	GENIC	homozygous	54258044
7	139143937	139143938	A	T	12	GENIC	homozygous	54145827
7	139145600	139145601	A	G	15	GENIC	possibly homozygous	54145831
7	139145916	139145917	A	G	22	GENIC	homozygous	54145833
7	139146237	139146238	A	G	20	GENIC	homozygous	54145835
7	139147045	139147046	T	G	12	GENIC	heterozygous	54145837
7	139147750	139147751	C	A	2	GENIC	heterozygous	55015782
7	139147774	139147775	C	G	4	GENIC	homozygous	54145908
7	139148089	139148090	A	G	1	GENIC	homozygous	54145922
7	139148288	139148290	GT	--	3	GENIC	heterozygous	54145932
7	139149093	139149094	C	A	22	GENIC	possibly homozygous	54145934
7	139152790	139152791	G	A	17	GENIC	homozygous	54145942
7	139154256	139154257	T	TCTGGATAGAAGCCTGAAG	2	GENIC	homozygous	54145954
7	139155232	139155238	GAAGAA	------	9	GENIC	homozygous	54145956