chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	50530360	50530361	G	A	27	GENIC	possibly homozygous	114890182
13	50530503	50530504	G	A	29	GENIC	homozygous	114340704
13	50531089	50531090	G	C	23	GENIC	homozygous	114340706
13	50531351	50531355	GTTT		17	GENIC	homozygous	129052769
13	50531632	50531633	C	T	23	GENIC	homozygous	114890184
13	50531949	50531950	C	T	27	GENIC	homozygous	114340710
13	50533753	50533754	T	C	32	GENIC	homozygous	114340715
13	50534211	50534212	C	T	29	GENIC	homozygous	114890186
13	50534382	50534389	ACCCCAG		31	GENIC	homozygous	131126386
13	50536215	50536216	C	A	28	GENIC	homozygous	114890188
13	50536435	50536436	G	A	18	GENIC	homozygous	114890190