chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	50482218	50482219	G	A	32	GENIC	homozygous	114340522
13	50483086	50483087	T	C	23	GENIC	homozygous	114671388
13	50483423	50483424	C	T	30	GENIC	homozygous	114671390
13	50484114	50484115	T	C	29	GENIC	homozygous	114340526
13	50484706	50484707	G	A	39	GENIC	homozygous	114762238
13	50485074	50485075	T	C	12	GENIC	homozygous	114671392
13	50485513	50485514	T	C	28	GENIC	homozygous	114671396
13	50485723	50485724	T	G	43	GENIC	homozygous	114671398
13	50485870	50485871	G	A	29	GENIC	homozygous	114671400
13	50485902	50485903	C	T	19	GENIC	homozygous	114671402
13	50485920	50485921	T	A	24	GENIC	homozygous	114671404
13	50486507	50486508	T	C	29	GENIC	homozygous	114762240
13	50486656	50486657	A	G	25	GENIC	homozygous	114340528
13	50488345	50488346	T	C	34	GENIC	homozygous	114340530
13	50488502	50488503	C	T	46	GENIC	homozygous	114340532
13	50488596	50488597	T	C	39	GENIC	homozygous	114340534
13	50489065	50489066	G	A	32	GENIC	homozygous	114340536
13	50489182	50489183	A	G	32	GENIC	homozygous	114340538
13	50489426	50489427	T	G	33	GENIC	homozygous	114340540
13	50490279	50490280	T	C	36	GENIC	homozygous	114340542
13	50491065	50491066	G	A	37	GENIC	homozygous	114762242
13	50493104	50493105	G	A	51	GENIC	homozygous	114340566
13	50493269	50493270	C	T	33	GENIC	homozygous	114340568
13	50494477	50494478	G	A	39	GENIC	homozygous	114762244
13	50495040	50495041	A	T	29	GENIC	homozygous	114762246
13	50495166	50495167	A	T	19	GENIC	homozygous	114340572
13	50495211	50495212	G	T	26	GENIC	homozygous	114340574
13	50495760	50495761	A	T	21	GENIC	homozygous	114340576
13	50496052	50496053	G	A	39	GENIC	homozygous	114340578
13	50496488	50496489	T	C	31	GENIC	homozygous	114762248
13	50496698	50496699	T	A	31	GENIC	homozygous	114549955
13	50498621	50498622	T	G	37	GENIC	homozygous	114340580
13	50498950	50498951	C	G	16	GENIC	homozygous	114340582