chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	50503225	50503226	G	A	35	GENIC	homozygous	114340603
13	50503539	50503540	G	A	38	GENIC	homozygous	114340605
13	50504347	50504348	T	C	28	GENIC	homozygous	114340611
13	50504459	50504460	T	C	20	GENIC	homozygous	114340613
13	50504767	50504768	G	A	32	GENIC	homozygous	114340615
13	50505563	50505564	G	A	39	GENIC	homozygous	114762250
13	50505720	50505721	T	C	37	GENIC	homozygous	114340619
13	50505769	50505770	T	C	31	GENIC	homozygous	114340621
13	50505841	50505842	G	C	30	GENIC	homozygous	114340623
13	50505888	50505889	T	C	25	GENIC	homozygous	114340624
13	50506251	50506252	A	G	30	GENIC	homozygous	114340626
13	50506355	50506356	A	G	31	GENIC	homozygous	114340628
13	50506492	50506493	C	T	28	GENIC	homozygous	114340630
13	50508870	50508871	C	T	20	GENIC	homozygous	114340632
13	50508941	50508942	T	C	21	GENIC	homozygous	114340634
13	50508972	50508973	T	C	26	GENIC	homozygous	114762252
13	50509431	50509432	G	A	18	GENIC	homozygous	114549956
13	50509748	50509749	T	C	25	GENIC	homozygous	114340640
13	50509903	50509904	G	A	26	GENIC	homozygous	114762254
13	50510397	50510398	T	G	35	GENIC	homozygous	114340644