chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	155029744	155029745	C	G	8	GENIC	homozygous	56131215
5	155029951	155029952	T	C	12	GENIC	homozygous	56238041
5	155030634	155030635	A	T	18	GENIC	homozygous	56131220
5	155030905	155030906	T	C	21	GENIC	homozygous	56131221
5	155031551	155031552	A	G	24	GENIC	homozygous	56131222
5	155031605	155031606	T	C	14	GENIC	homozygous	56131226
5	155031732	155031733	G	A	20	GENIC	homozygous	56131227
5	155034774	155034775	C	T	13	GENIC	homozygous	56238042
5	155036437	155036438	G	A	16	GENIC	homozygous	56238043
5	155036777	155036778	A	G	19	GENIC	homozygous	56238044
5	155039868	155039869	T	C	18	GENIC	homozygous	56131253
5	155041896	155041897	C	T	16	GENIC	homozygous	56238045
5	155042774	155042775	A	G	14	GENIC	homozygous	56131259
5	155042981	155042982	T	G	10	GENIC	homozygous	56238046
5	155043287	155043288	A	G	15	GENIC	homozygous	56131260
5	155043331	155043332	T	C	19	GENIC	homozygous	56238047
5	155043610	155043611	G	A	13	GENIC	homozygous	56238048
5	155043660	155043661	G	T	10	GENIC	homozygous	56131262