chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	31242260	31242261	T	C	53	GENIC	homozygous	139266472
13	31243689	31243690	C	T	45	GENIC	homozygous	139266473
13	31244717	31244718	G		29	GENIC	homozygous	139166888
13	31244808	31244809	T	C	8	GENIC	homozygous	139266474
13	31244970	31244971	T		31	GENIC	possibly homozygous	139166889
13	31245250	31245251	C		6	GENIC	heterozygous	403334384
13	31245250	31245251	C	T	6	GENIC	homozygous	403334385
13	31245250	31245251	C	G	6	GENIC	heterozygous	403334386
13	31245843	31245844	G	C	47	GENIC	homozygous	139266475
13	31245944	31245945	A	G	38	GENIC	homozygous	139266476
13	31246122	31246123	C	G	44	GENIC	homozygous	139266477
13	31246459	31246460	C	T	42	GENIC	homozygous	139266478
13	31248576	31248576		TT	39	GENIC	homozygous	139166893
13	31249494	31249494		C	40	GENIC	homozygous	139166894
13	31247806	31247806		TG	24	GENIC	possibly homozygous	143547508
13	31247144	31247145	A	G	40	GENIC	homozygous	139266479
13	31248631	31248632	G	T	29	GENIC	homozygous	139266480
13	31248750	31248751	G	A	46	GENIC	homozygous	139266481
13	31249280	31249281	G	T	47	GENIC	homozygous	139266482