chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	50875311	50875312	G	A	43	GENIC	homozygous	114341825
13	50876967	50876968	A	G	32	GENIC	homozygous	114341827
13	50876973	50876974	A	G	30	GENIC	homozygous	114341829
13	50880969	50880970	A	C	17	GENIC	possibly homozygous	118450701
13	50881582	50881583	T	C	31	GENIC	homozygous	114341831
13	50881639	50881640	G	A	28	GENIC	homozygous	114341833
13	50881792	50881793	A	G	48	GENIC	homozygous	114341835
13	50882137	50882138	G	T	35	GENIC	homozygous	114341837
13	50882231	50882232	T	C	33	GENIC	homozygous	114341839
13	50882344	50882345	C	T	44	GENIC	homozygous	114341841
13	50882434	50882435	G	A	37	GENIC	homozygous	114341843
13	50883094	50883095	A	G	29	GENIC	homozygous	114341845
13	50883798	50883799	A	G	27	GENIC	homozygous	114341847
13	50883824	50883825	G	A	25	GENIC	heterozygous	118450702
13	50883831	50883832	G	A	25	GENIC	heterozygous	114671833