chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	32615951	32615952	T	TA	21	GENIC	homozygous	49707496
13	32616012	32616013	C	T	17	GENIC	homozygous	49707497
13	32616101	32616102	G	A	22	GENIC	possibly homozygous	49707498
13	32617386	32617387	T	C	19	GENIC	homozygous	49707499
13	32617656	32617657	C	G	24	GENIC	possibly homozygous	49707500
13	32618379	32618380	C	T	11	GENIC	possibly homozygous	49707501
13	32618657	32618658	C	T	20	GENIC	possibly homozygous	49707502
13	32619436	32619439	AAA	---	7	GENIC	heterozygous	50189813
13	32619437	32619439	AA	--	7	GENIC	heterozygous	49707503
13	32621832	32621833	C	A	20	GENIC	possibly homozygous	49707504
13	32621869	32621870	C	T	22	GENIC	homozygous	49707505
13	32622672	32622673	A	T	19	GENIC	possibly homozygous	49707506
13	32622843	32622844	A	C	14	GENIC	homozygous	49707507
13	32624335	32624336	G	A	17	GENIC	homozygous	49707508
13	32625182	32625183	T	TG	15	GENIC	possibly homozygous	49707512
13	32625639	32625640	A	G	18	GENIC	possibly homozygous	49707513
13	32626305	32626306	T	C	21	GENIC	homozygous	49707514
13	32626437	32626438	T	TG	10	GENIC	homozygous	49707515
13	32627178	32627179	C	T	13	GENIC	homozygous	49707518
13	32627365	32627366	G	GT	5	GENIC	homozygous	49707519
13	32627566	32627567	G	A	24	GENIC	possibly homozygous	49707520
13	32627701	32627702	A	T	30	GENIC	homozygous	49707521
13	32627954	32627955	T	C	27	GENIC	homozygous	49707522
13	32628695	32628696	C	T	19	GENIC	possibly homozygous	49707523
13	32630274	32630275	T	A	8	GENIC	possibly homozygous	49707524
13	32630331	32630332	C	A	10	GENIC	possibly homozygous	49707525
13	32630937	32630938	G	A	14	GENIC	homozygous	49707526
13	32631967	32631968	G	A	21	GENIC	homozygous	49707527
13	32632238	32632239	T	-	17	GENIC	homozygous	49707528
13	32633268	32633269	T	C	23	GENIC	possibly homozygous	49707529