chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	31242260	31242261	T	C	51	GENIC	homozygous	139266472
13	31243689	31243690	C	T	39	GENIC	homozygous	139266473
13	31244717	31244718	G		37	GENIC	homozygous	139166888
13	31244808	31244809	T	C	22	GENIC	homozygous	139266474
13	31245843	31245844	G	C	57	GENIC	homozygous	139266475
13	31245944	31245945	A	G	48	GENIC	homozygous	139266476
13	31246122	31246123	C	G	47	GENIC	homozygous	139266477
13	31246459	31246460	C	T	45	GENIC	homozygous	139266478
13	31247144	31247145	A	G	49	GENIC	homozygous	139266479
13	31247818	31247818		T	32	GENIC	homozygous	139166891
13	31244970	31244971	T		35	GENIC	possibly homozygous	139166889
13	31245285	31245328	AGGGCCTTGCGCTTGCTAGGCAAGCGCTCTACCACTGAGCTAA		23	GENIC	homozygous	139166890
13	31247819	31247819		T	32	GENIC	homozygous	139166892
13	31248576	31248576		TT	48	GENIC	homozygous	139166893
13	31248631	31248632	G	T	50	GENIC	homozygous	139266480
13	31248750	31248751	G	A	51	GENIC	homozygous	139266481
13	31249280	31249281	G	T	51	GENIC	possibly homozygous	139266482
13	31249494	31249494		C	48	GENIC	homozygous	139166894