chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	50913649	50913650	A	AC	7	INTERGENIC	homozygous	49755710
13	50913689	50913690	C	T	11	INTERGENIC	homozygous	50035342
13	50913817	50913818	A	G	26	INTERGENIC	homozygous	50035344
13	50913853	50913854	G	T	27	INTERGENIC	homozygous	50035346
13	50913866	50913867	C	T	25	INTERGENIC	homozygous	50035348
13	50913900	50913901	A	G	19	INTERGENIC	possibly homozygous	50035350
13	50913939	50913940	G	T	21	INTERGENIC	homozygous	50035352
13	50914256	50914257	T	C	25	INTERGENIC	homozygous	50035354
13	50914458	50914459	G	-	12	INTERGENIC	homozygous	50035356
13	50914476	50914477	A	-	12	INTERGENIC	homozygous	50035358
13	50914507	50914508	T	C	14	INTERGENIC	homozygous	50035360
13	50914818	50914819	T	C	19	INTERGENIC	homozygous	50035362
13	50915003	50915004	A	T	21	INTERGENIC	homozygous	50035364
13	50915109	50915110	G	A	31	INTERGENIC	homozygous	50035366
13	50915167	50915168	C	T	32	INTERGENIC	homozygous	50035368
13	50915200	50915201	G	A	32	INTERGENIC	homozygous	50035370
13	50915288	50915289	G	C	40	INTERGENIC	homozygous	50035371
13	50915401	50915402	A	T	33	INTERGENIC	homozygous	50035373
13	50915642	50915643	C	A	21	INTERGENIC	homozygous	50035375
13	50916592	50916593	T	C	18	INTERGENIC	homozygous	50035377
13	50916593	50916594	G	A	18	INTERGENIC	homozygous	50035379
13	50916666	50916667	T	C	25	INTERGENIC	homozygous	50035381
13	50916900	50916902	AA	--	19	INTERGENIC	homozygous	50035383