chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	53000668	53000668		G	34	GENIC	homozygous	129053995
13	53000680	53000681	A		40	GENIC	homozygous	129053996
13	53000684	53000684		TC	39	GENIC	homozygous	129053997
13	53000687	53000687		C	37	GENIC	homozygous	129053998
13	53000690	53000691	A		35	GENIC	homozygous	129053999
13	53000692	53000692		TG	35	GENIC	homozygous	129054000
13	53000695	53000695		G	36	GENIC	homozygous	129054001
13	53000713	53000714	G		43	GENIC	homozygous	129054002
13	53000720	53000721	A	G	45	GENIC	homozygous	118451067
13	53000736	53000736		C	42	GENIC	homozygous	129054003
13	53000743	53000744	C	T	42	GENIC	homozygous	115010103
13	53000744	53000745	T	C	41	GENIC	homozygous	123735171
13	53000791	53000792	T		46	GENIC	homozygous	129054004
13	53000911	53000911		T	44	GENIC	homozygous	129054005
13	53000916	53000917	A	C	45	GENIC	homozygous	114550774
13	53000937	53000938	G		42	GENIC	homozygous	129054006
13	53000957	53000957		A	36	GENIC	homozygous	129054007
13	53000961	53000962	T		38	GENIC	homozygous	129054008
13	53000977	53000977		T	40	GENIC	homozygous	129054009
13	53000984	53000984		CC	39	GENIC	homozygous	129054010
13	53001016	53001016		T	45	GENIC	homozygous	129054011
13	53001023	53001024	A		43	GENIC	homozygous	129054012
13	53001026	53001027	G		43	GENIC	homozygous	129054013
13	53001035	53001035		T	41	GENIC	homozygous	129054014
13	53001039	53001039		T	40	GENIC	homozygous	129054015
13	53001040	53001040		T	39	GENIC	homozygous	129054016
13	53003268	53003269	T	C	24	GENIC	homozygous	114346638
13	53003270	53003271	T	G	23	GENIC	homozygous	114346640
13	53003271	53003272	T	G	23	GENIC	homozygous	114346642
13	53003272	53003273	T	G	23	GENIC	homozygous	114346644
13	53001028	53001029	G	T	42	GENIC	homozygous	114617580