chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	79696841	79696842	G	A	34	GENIC	homozygous	115119708
13	79697969	79697970	A	G	47	GENIC	homozygous	114404221
13	79698283	79698284	C	T	46	GENIC	possibly homozygous	114929904
13	79698784	79698785	T	C	47	GENIC	homozygous	114404225
13	79702190	79702191	T	C	52	GENIC	homozygous	114929906
13	79703559	79703560	C	G	42	GENIC	possibly homozygous	114929908
13	79704619	79704620	G	A	56	GENIC	possibly homozygous	114404253
13	79708373	79708374	T	C	51	GENIC	homozygous	114404304
13	79710419	79710420	A	G	56	GENIC	homozygous	114404319
13	79711540	79711541	G	A	56	GENIC	homozygous	114404326
13	79712670	79712671	C	G	41	GENIC	homozygous	114404338
13	79715799	79715800	A	G	52	GENIC	possibly homozygous	114929910
13	79716813	79716814	C	T	50	GENIC	homozygous	114775565
13	79717033	79717034	C	T	57	GENIC	homozygous	114775567
13	79717155	79717156	C	T	48	GENIC	homozygous	114900407
13	79717289	79717290	G	A	51	GENIC	homozygous	114775569
13	79717441	79717442	C	T	55	GENIC	homozygous	114775571
13	79717460	79717461	T	C	53	GENIC	homozygous	114775573
13	79717539	79717540	C	A	53	GENIC	homozygous	114775575
13	79717566	79717567	A	T	53	GENIC	homozygous	114775577