chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	159639681	159639682	G	T	34	GENIC	homozygous	114073074
5	159639794	159639795	C	T	50	GENIC	possibly homozygous	114073075
5	159641223	159641224	G	A	38	GENIC	homozygous	114073076
5	159642805	159642806	C	T	36	GENIC	homozygous	114073077
5	159648206	159648207	C	T	56	GENIC	homozygous	114073078
5	159648732	159648733	C	T	51	GENIC	homozygous	114073079
5	159648780	159648781	G	A	40	GENIC	homozygous	114073080
5	159649309	159649310	A	G	34	GENIC	homozygous	114073081
5	159650383	159650384	G	A	41	GENIC	homozygous	114073082
5	159650944	159650945	T	A	56	GENIC	homozygous	114073083
5	159651012	159651013	T	C	46	GENIC	homozygous	114073084
5	159651791	159651792	A	G	52	GENIC	homozygous	114073085
5	159653029	159653030	T	C	32	GENIC	homozygous	114073086
5	159655029	159655030	C	T	54	GENIC	homozygous	114073087
5	159656888	159656889	G	A	41	GENIC	possibly homozygous	114073088
5	159661740	159661741	A	T	42	GENIC	homozygous	114073089