chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	36151595	36151596	A	G	65	GENIC	possibly homozygous	114313952
13	36151598	36151599	C	A	63	GENIC	possibly homozygous	114313953
13	36151966	36151967	A	C	39	GENIC	homozygous	114528118
13	36152074	36152075	T	G	45	GENIC	homozygous	114920359
13	36152196	36152197	A	G	6	GENIC	homozygous	118494517
13	36152269	36152270	T	G	20	GENIC	homozygous	118446748
13	36152181	36152182	C	T	32	GENIC	homozygous	118446745
13	36152185	36152186	G	T	31	GENIC	homozygous	118446746
13	36152248	36152249	G	A	27	GENIC	homozygous	118446747
13	36152320	36152321	A	T	39	GENIC	homozygous	118446749
13	36152350	36152351	C	A	51	GENIC	homozygous	115099214
13	36152388	36152389	A	T	22	GENIC	homozygous	114313954
13	36154305	36154306	C	A	22	GENIC	homozygous	118446750
13	36154854	36154855	G	T	55	GENIC	homozygous	114313957
13	36155966	36155967	G	A	86	GENIC	heterozygous	118494518
13	36155989	36155990	G	A	88	GENIC	heterozygous	118494519
13	36155991	36155992	G	A	90	GENIC	heterozygous	118494521
13	36156044	36156045	G	T	59	GENIC	homozygous	118494523