chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	159929262	159929263	C	T	37	GENIC	homozygous	145563480
5	159936819	159936820	T	C	40	GENIC	homozygous	145563481
5	159937646	159937646		T	16	GENIC	possibly homozygous	145139580
5	159937855	159937856	A	G	13	GENIC	homozygous	145563483
5	159938070	159938071	A	G	23	GENIC	homozygous	145563484
5	159938572	159938573	T	C	37	GENIC	homozygous	145563485
5	159939067	159939068	T	G	37	GENIC	homozygous	149036817
5	159932273	159932275	GC		27	GENIC	homozygous	149031856
5	159938478	159938478		T	38	GENIC	homozygous	149031857
5	159932331	159932332	C	T	20	GENIC	homozygous	149036811
5	159932728	159932729	C	T	40	GENIC	homozygous	149036812
5	159937712	159937713	G	A	22	GENIC	homozygous	149036813
5	159938366	159938367	T	G	31	GENIC	homozygous	149036814
5	159938475	159938476	G	C	38	GENIC	homozygous	149036815
5	159938478	159938479	G	T	39	GENIC	homozygous	149036816
5	159938035	159938036	G		15	GENIC	homozygous	146772145
5	159939328	159939329	A	C	28	GENIC	homozygous	145563487
5	159939744	159939745	C	T	44	GENIC	homozygous	145563488
5	159939957	159939958	G	A	48	GENIC	homozygous	145563489
5	159940320	159940321	C	T	48	GENIC	homozygous	145563490
5	159940605	159940606	A	G	52	GENIC	homozygous	145563491
5	159940670	159940671	C	T	40	GENIC	homozygous	145563492