chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	57514032	57514033	T	C	34	GENIC	homozygous	46608872
18	57514139	57514140	G	A	34	GENIC	homozygous	46608874
18	57514283	57514284	C	T	41	GENIC	homozygous	46608876
18	57514337	57514338	A	G	33	GENIC	homozygous	46608877
18	57514487	57514488	A	G	38	GENIC	homozygous	46608881
18	57514522	57514523	C	CT	17	GENIC	possibly homozygous	46854834
18	57514580	57514581	C	CA	25	GENIC	homozygous	46939195
18	57514843	57514844	C	T	32	GENIC	homozygous	46939196
18	57514949	57514950	G	A	38	GENIC	homozygous	46939197
18	57515141	57515142	C	T	27	GENIC	homozygous	46939198
18	57515521	57515522	C	T	37	GENIC	homozygous	46939199
18	57515568	57515569	T	-	21	GENIC	homozygous	46854836
18	57515656	57515657	T	G	32	GENIC	homozygous	46688115