chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	53322862	53322863	C	T	21	GENIC	homozygous	114347677
13	53325231	53325232	C	T	14	GENIC	homozygous	114347683
13	53325333	53325334	T	C	32	GENIC	homozygous	114347685
13	53328859	53328860	C	T	29	GENIC	homozygous	114347689
13	53329405	53329406	A	G	22	GENIC	possibly homozygous	114347691
13	53329830	53329831	C	T	14	GENIC	homozygous	114347693
13	53330126	53330127	A	G	23	GENIC	homozygous	114347695
13	53330285	53330286	C	T	20	GENIC	homozygous	114347697
13	53331001	53331002	T	A	22	GENIC	homozygous	114550963
13	53331120	53331121	C	T	28	GENIC	homozygous	114673085
13	53331175	53331176	C	A	28	GENIC	homozygous	114673087
13	53331224	53331225	A	G	22	GENIC	homozygous	114550964
13	53331262	53331263	C	T	22	GENIC	homozygous	114673089
13	53331394	53331395	A	G	11	GENIC	homozygous	114550965
13	53331869	53331870	A	G	20	GENIC	homozygous	114550966
13	53331913	53331914	T	C	22	GENIC	homozygous	114550967
13	53332169	53332170	A	G	20	GENIC	homozygous	114550969
13	53332739	53332740	G	A	15	GENIC	homozygous	114347701
13	53332918	53332919	A	G	23	GENIC	homozygous	114347703
13	53333076	53333077	C	T	20	GENIC	homozygous	114550973
13	53333079	53333080	G	A	21	GENIC	homozygous	114673091