chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	27186768	27186769	C	A	37	GENIC	homozygous	114303563
13	27186791	27186792	G	A	40	GENIC	homozygous	114303564
13	27187605	27187606	A	G	53	GENIC	homozygous	114303565
13	27187924	27187925	G	A	25	GENIC	homozygous	114303567
13	27188345	27188346	T	A	46	GENIC	homozygous	114303568
13	27189129	27189130	C	T	42	GENIC	homozygous	114303569
13	27189615	27189616	T	C	31	GENIC	homozygous	114303570
13	27190080	27190081	G	A	55	GENIC	homozygous	114303571
13	27190085	27190086	A	C	58	GENIC	homozygous	114303572
13	27190203	27190204	C	T	66	GENIC	homozygous	114303573
13	27190705	27190706	T	A	53	GENIC	homozygous	114303574
13	27190940	27190941	T	A	43	GENIC	homozygous	114303575
13	27191020	27191021	C	A	42	GENIC	homozygous	114303576
13	27191114	27191115	A	T	52	GENIC	homozygous	114303577
13	27192044	27192045	A	G	42	GENIC	homozygous	114303578
13	27192295	27192296	C	T	49	GENIC	homozygous	118438073
13	27192637	27192638	G	A	64	GENIC	possibly homozygous	118438074
13	27192991	27192992	T	C	39	GENIC	homozygous	114303579