chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	79379203	79379204	A	T	29	GENIC	possibly homozygous	115030555
13	79380022	79380023	T	A	22	GENIC	homozygous	115183619
13	79380263	79380264	A	G	20	GENIC	homozygous	114689964
13	79380307	79380308	A	G	21	GENIC	homozygous	114775251
13	79381302	79381303	G	A	19	GENIC	homozygous	114689971
13	79381304	79381305	A	G	19	GENIC	homozygous	114689972
13	79381532	79381533	C	T	27	GENIC	homozygous	115183621
13	79382862	79382863	T	C	21	GENIC	homozygous	114402859
13	79380648	79380649	G	A	13	GENIC	possibly homozygous	114402853
13	79381093	79381094	G	A	18	GENIC	possibly homozygous	114402855
13	79381767	79381768	A	G	27	GENIC	possibly homozygous	114402857
13	79383614	79383615	G	A	20	GENIC	possibly homozygous	114775263
13	79387854	79387855	G	A	27	GENIC	homozygous	115183623
13	79388276	79388277	T	A	17	GENIC	homozygous	115183625
13	79388383	79388384	T	A	17	GENIC	homozygous	114690029
13	79388384	79388385	T	G	18	GENIC	homozygous	114690030