chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5712438	5712439	A	G	52	GENIC	homozygous	109078982
20	5713150	5713151	C	G	37	GENIC	homozygous	109078984
20	5713177	5713178	C	A	39	GENIC	homozygous	109234334
20	5713198	5713199	G	A	45	GENIC	homozygous	109234335
20	5714317	5714318	C	A	57	GENIC	homozygous	109078988
20	5717447	5717448	G	A	47	GENIC	homozygous	109234337
20	5718229	5718230	T	G	62	GENIC	possibly homozygous	109078994
20	5718442	5718443	C	T	52	GENIC	homozygous	109234338
20	5720243	5720244	A	G	54	GENIC	homozygous	109234339
20	5720855	5720856	T	G	50	GENIC	homozygous	109078996
20	5720861	5720862	C	T	48	GENIC	homozygous	109234340
20	5721455	5721456	G	A	61	GENIC	homozygous	109234341
20	5722271	5722272	T	C	50	GENIC	homozygous	109078998
20	5723539	5723540	G	A	57	GENIC	possibly homozygous	109234342
20	5714886	5714887	C	T	65	GENIC	possibly homozygous	109390546
20	5718010	5718011	T	C	49	GENIC	homozygous	109390547
20	5722714	5722715	G	A	47	GENIC	homozygous	109390548
20	5722823	5722824	G		60	GENIC	homozygous	129653867
20	5723571	5723571		AAGG	52	GENIC	possibly homozygous	131228192
20	5718017	5718019	AG		49	GENIC	homozygous	131555389
20	5721168	5721169	G		39	GENIC	homozygous	129653866
20	5722604	5722608	CTAT		60	GENIC	homozygous	131228191