chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	50503225	50503226	G	A	41	GENIC	homozygous	114340603
13	50503539	50503540	G	A	34	GENIC	homozygous	114340605
13	50503592	50503593	C	T	32	GENIC	homozygous	114340607
13	50503859	50503860	G	A	31	GENIC	homozygous	114340609
13	50504347	50504348	T	C	39	GENIC	homozygous	114340611
13	50504459	50504460	T	C	39	GENIC	homozygous	114340613
13	50504767	50504768	G	A	46	GENIC	homozygous	114340615
13	50505501	50505502	G	A	42	GENIC	homozygous	118450632
13	50505720	50505721	T	C	37	GENIC	homozygous	114340619
13	50505769	50505770	T	C	34	GENIC	homozygous	114340621
13	50505841	50505842	G	C	33	GENIC	homozygous	114340623
13	50505888	50505889	T	C	26	GENIC	homozygous	114340624
13	50506251	50506252	A	G	41	GENIC	homozygous	114340626
13	50506355	50506356	A	G	57	GENIC	homozygous	114340628
13	50506492	50506493	C	T	34	GENIC	homozygous	114340630
13	50508870	50508871	C	T	36	GENIC	homozygous	114340632
13	50508941	50508942	T	C	28	GENIC	homozygous	114340634
13	50509004	50509005	G	C	33	GENIC	homozygous	114340636
13	50509363	50509364	C	T	17	GENIC	homozygous	114340638
13	50509431	50509432	G	A	13	GENIC	homozygous	114549956
13	50509748	50509749	T	C	26	GENIC	homozygous	114340640
13	50510138	50510139	C	T	27	GENIC	homozygous	114340642
13	50510397	50510398	T	G	28	GENIC	homozygous	114340644
13	50512198	50512199	C	T	57	GENIC	heterozygous	118498347