chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	50619536	50619537	T	C	21	INTERGENIC	homozygous	114671439
13	50620236	50620237	T	C	37	INTERGENIC	homozygous	114340888
13	50620512	50620513	C	T	20	INTERGENIC	homozygous	114671443
13	50625422	50625423	G	A	24	INTERGENIC	homozygous	114340894
13	50626266	50626267	G	A	29	INTERGENIC	homozygous	114671445
13	50627441	50627442	C	T	26	INTERGENIC	homozygous	114340896
13	50627988	50627989	G	A	28	INTERGENIC	homozygous	114340898
13	50628066	50628067	G	A	12	INTERGENIC	homozygous	114671447
13	50628440	50628441	G	T	27	INTERGENIC	homozygous	114671449
13	50628570	50628571	T	C	24	INTERGENIC	homozygous	114340900
13	50628573	50628574	C	T	23	INTERGENIC	homozygous	114340902
13	50629190	50629191	C	T	27	INTERGENIC	homozygous	114340904
13	50629302	50629303	C	T	13	INTERGENIC	homozygous	114340906
13	50629644	50629645	A	G	29	INTERGENIC	homozygous	114671451
13	50630261	50630262	C	A	34	INTERGENIC	homozygous	114671453
13	50630395	50630396	A	G	24	INTERGENIC	homozygous	114340908
13	50630995	50630996	C	T	40	INTERGENIC	homozygous	114340910
13	50631412	50631413	T	C	30	INTERGENIC	homozygous	114340912
13	50631847	50631848	T	C	26	INTERGENIC	homozygous	114671455
13	50632040	50632041	A	C	21	INTERGENIC	homozygous	114671457
13	50632775	50632776	C	T	32	INTERGENIC	homozygous	114671459