chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	51662342	51662343	T	C	43	GENIC	homozygous	110347470
18	51663345	51663346	G	A	64	GENIC	possibly homozygous	110347472
18	51663460	51663461	A	T	23	GENIC	heterozygous	110537314
18	51664210	51664211	G	A	52	GENIC	possibly homozygous	110347474
18	51664339	51664340	C	T	56	GENIC	possibly homozygous	110347476
18	51664528	51664529	T	G	53	GENIC	homozygous	110347478
18	51664659	51664660	C	A	49	GENIC	possibly homozygous	110347480
18	51664722	51664723	T	C	51	GENIC	homozygous	110347482
18	51665376	51665377	A	G	56	GENIC	homozygous	110347484
18	51666167	51666168	G	A	48	GENIC	homozygous	110347486
18	51666340	51666341	C	T	71	GENIC	homozygous	110347488
18	51666651	51666652	G	A	45	GENIC	homozygous	110347490
18	51667353	51667354	G	T	68	GENIC	possibly homozygous	110347492
18	51673853	51673854	A	T	48	GENIC	homozygous	110347496
18	51668418	51668419	G	T	59	GENIC	homozygous	110347494
18	51670682	51670683	A	G	27	GENIC	possibly homozygous	110703151
18	51667983	51667984	A	G	51	GENIC	homozygous	110473063
18	51662949	51662950	A	G	37	GENIC	homozygous	119493158
18	51665922	51665923	T	G	43	GENIC	possibly homozygous	119493159
18	51672264	51672265	G	A	51	GENIC	heterozygous	119493160
18	51670358	51670359	A	G	51	GENIC	possibly homozygous	110813404
18	51670686	51670687	A	G	28	GENIC	heterozygous	119530842
18	51677683	51677684	G	A	54	GENIC	possibly homozygous	110653388