chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	87436646	87436647	G	-	14	GENIC	homozygous	49848987
13	87437570	87437571	A	T	43	GENIC	homozygous	49848988
13	87437693	87437694	C	T	52	GENIC	homozygous	49848989
13	87437877	87437878	A	G	62	GENIC	homozygous	49848990
13	87437882	87437883	T	C	67	GENIC	homozygous	49848991
13	87438264	87438265	G	A	46	GENIC	possibly homozygous	49848992
13	87439019	87439020	G	A	25	GENIC	homozygous	49848993
13	87439202	87439203	G	A	34	GENIC	possibly homozygous	49848994
13	87439617	87439619	TC	--	37	GENIC	heterozygous	49848995
13	87439621	87439623	TC	--	42	GENIC	heterozygous	49848996
13	87439626	87439627	C	G	49	GENIC	heterozygous	49848997
13	87439953	87439957	TTAT	----	4	GENIC	homozygous	49848998
13	87440070	87440071	G	A	23	GENIC	homozygous	49848999
13	87441546	87441547	G	A	50	GENIC	homozygous	49849000
13	87443381	87443382	A	C	54	GENIC	heterozygous	49849001
13	87444345	87444346	T	-	31	GENIC	homozygous	49849002
13	87445217	87445218	G	A	41	GENIC	heterozygous	49849003
13	87445217	87445218	G	GTGTA	18	GENIC	homozygous	49849004
13	87445333	87445334	C	T	30	GENIC	homozygous	49849005
13	87448026	87448027	C	CT	12	GENIC	heterozygous	49849006
13	87448051	87448052	C	T	35	GENIC	heterozygous	49849007
13	87448072	87448073	T	C	29	GENIC	possibly homozygous	49849008