chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	142087849	142087850	A	G	47	GENIC	homozygous	109049763
1	142088675	142088676	C		41	GENIC	possibly homozygous	130520089
1	142091637	142091638	G	A	46	GENIC	homozygous	108937351
1	142092365	142092366	T		37	GENIC	homozygous	127439686
1	142089543	142089543		CTTT	22	GENIC	homozygous	130823693
1	142095281	142095282	A	G	51	GENIC	homozygous	108262659
1	142095924	142095924		A	54	GENIC	homozygous	130823694
1	142096564	142096565	G	T	51	GENIC	homozygous	109049765
1	142097858	142097859	G	T	11	GENIC	homozygous	108262661
1	142100410	142100411	T	G	47	GENIC	homozygous	108262663
1	142100485	142100486	T	C	50	GENIC	homozygous	109327838
1	142100490	142100491	A	C	49	GENIC	homozygous	109049770
1	142101397	142101398	G	C	59	GENIC	homozygous	109049771
1	142104556	142104556		TT	53	GENIC	homozygous	130823695
1	142104770	142104771	T	C	54	GENIC	homozygous	108262665
1	142105585	142105586	G	A	57	GENIC	homozygous	109049772
1	142098430	142098431	T	G	8	GENIC	homozygous	108743914
1	142098434	142098435	T	G	8	GENIC	homozygous	108743916