chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	4816862	4816863	C		66	GENIC	homozygous	129979676
20	4817135	4817138	CTT		59	GENIC	possibly homozygous	129979677
20	4817763	4817764	A	G	71	GENIC	possibly homozygous	130032841
20	4819177	4819178	T	G	67	GENIC	homozygous	130032843
20	4819241	4819242	T	C	66	GENIC	homozygous	130032844
20	4819253	4819254	C	A	60	GENIC	homozygous	130032845
20	4819860	4819861	G	A	55	GENIC	homozygous	130032846
20	4820019	4820020	T	C	66	GENIC	homozygous	130032848
20	4820350	4820351	A	G	77	GENIC	homozygous	130032849
20	4820401	4820402	A	G	77	GENIC	homozygous	130032850
20	4821313	4821314	G	A	73	GENIC	homozygous	130032851
20	4821372	4821373	G	T	67	GENIC	homozygous	130032852
20	4821379	4821380	C	T	69	GENIC	homozygous	130032853
20	4822320	4822321	A	G	63	GENIC	homozygous	130032854
20	4822860	4822861	G	A	46	GENIC	homozygous	130032855
20	4823142	4823143	G		55	GENIC	possibly homozygous	129979679
20	4823059	4823060	C	T	61	GENIC	homozygous	140510747
20	4823001	4823014	CGGAGGAGGCGGT		61	GENIC	homozygous	140483398
20	4823019	4823021	CC		62	GENIC	homozygous	140483399