chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	155029744	155029745	C	G	27	GENIC	homozygous	56131215
5	155029951	155029952	T	C	32	GENIC	homozygous	56238041
5	155030634	155030635	A	T	24	GENIC	homozygous	56131220
5	155030905	155030906	T	C	33	GENIC	homozygous	56131221
5	155031551	155031552	A	G	28	GENIC	homozygous	56131222
5	155031605	155031606	T	C	28	GENIC	homozygous	56131226
5	155031732	155031733	G	A	27	GENIC	homozygous	56131227
5	155034774	155034775	C	T	41	GENIC	possibly homozygous	56238042
5	155034995	155034996	C	CA	7	GENIC	heterozygous	56495172
5	155036437	155036438	G	A	35	GENIC	homozygous	56238043
5	155036777	155036778	A	G	28	GENIC	homozygous	56238044
5	155038850	155038851	A	-	11	GENIC	homozygous	55803824
5	155039309	155039310	C	-	5	GENIC	heterozygous	56751970
5	155039868	155039869	T	C	46	GENIC	homozygous	56131253
5	155041896	155041897	C	T	33	GENIC	homozygous	56238045
5	155042774	155042775	A	G	51	GENIC	homozygous	56131259
5	155042981	155042982	T	G	41	GENIC	homozygous	56238046
5	155043287	155043288	A	G	32	GENIC	homozygous	56131260
5	155043331	155043332	T	C	33	GENIC	homozygous	56238047
5	155043610	155043611	G	A	24	GENIC	homozygous	56238048
5	155043660	155043661	G	T	21	GENIC	homozygous	56131262
5	155044562	155044563	T	-	13	GENIC	heterozygous	55803825
5	155045228	155045229	G	GA	23	GENIC	heterozygous	57113337