chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	50481262	50481263	G	A	26	GENIC	homozygous	126066449
13	50481512	50481513	G	A	19	GENIC	homozygous	126066450
13	50482216	50482217	C	T	24	GENIC	homozygous	126066451
13	50484112	50484113	A	G	14	GENIC	homozygous	126066452
13	50486654	50486655	T	C	8	GENIC	homozygous	126066453
13	50488343	50488344	A	G	9	GENIC	homozygous	126066454
13	50488500	50488501	G	A	12	GENIC	homozygous	126066455
13	50488594	50488595	A	G	27	GENIC	homozygous	126066456
13	50489063	50489064	C	T	23	GENIC	possibly homozygous	126066457
13	50489180	50489181	T	C	21	GENIC	homozygous	126066458
13	50489424	50489425	A	C	11	GENIC	homozygous	126066459
13	50490135	50490136	C	G	4	GENIC	homozygous	126066460
13	50490277	50490278	A	G	22	GENIC	homozygous	126066461
13	50490759	50490760	C	T	19	GENIC	homozygous	126066462
13	50491609	50491610	G	T	14	GENIC	homozygous	126066463
13	50491659	50491660	G	A	19	GENIC	homozygous	126066464
13	50491804	50491805	A	G	12	GENIC	homozygous	126066465
13	50491806	50491807	T	C	11	GENIC	homozygous	114340550
13	50491912	50491913	C	T	22	GENIC	homozygous	126066466
13	50492044	50492045	C	T	24	GENIC	homozygous	126066467
13	50492185	50492186	A	G	29	GENIC	homozygous	126066468
13	50492626	50492627	A	G	19	GENIC	homozygous	126066469
13	50493018	50493019	G	A	19	GENIC	homozygous	126066470
13	50493102	50493103	C	T	15	GENIC	homozygous	126066471
13	50493267	50493268	G	A	13	GENIC	homozygous	126066472
13	50494804	50494805	T	C	20	GENIC	homozygous	126066473
13	50495164	50495165	T	A	10	GENIC	homozygous	126066474
13	50495209	50495210	C	A	20	GENIC	homozygous	126066475
13	50495758	50495759	T	A	16	GENIC	homozygous	126066476
13	50496050	50496051	C	T	19	GENIC	homozygous	126066477
13	50496696	50496697	A	T	17	GENIC	homozygous	126066478
13	50498619	50498620	A	C	15	GENIC	homozygous	126066479
13	50498948	50498949	G	C	6	GENIC	homozygous	126066480