chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	4816862	4816863	C		30	GENIC	homozygous	129979676
20	4817135	4817138	CTT		24	GENIC	homozygous	129979677
20	4817763	4817764	A	G	20	GENIC	homozygous	130032841
20	4818189	4818190	A	T	20	GENIC	homozygous	130032842
20	4819177	4819178	T	G	19	GENIC	homozygous	130032843
20	4819241	4819242	T	C	21	GENIC	homozygous	130032844
20	4819253	4819254	C	A	22	GENIC	homozygous	130032845
20	4819860	4819861	G	A	20	GENIC	homozygous	130032846
20	4819938	4819939	C	T	22	GENIC	homozygous	130032847
20	4820019	4820020	T	C	23	GENIC	homozygous	130032848
20	4820033	4820045	GGTGTGACCCCA		27	GENIC	homozygous	129979678
20	4820350	4820351	A	G	19	GENIC	homozygous	130032849
20	4820401	4820402	A	G	26	GENIC	homozygous	130032850
20	4821313	4821314	G	A	28	GENIC	homozygous	130032851
20	4821372	4821373	G	T	26	GENIC	homozygous	130032852
20	4821379	4821380	C	T	27	GENIC	homozygous	130032853
20	4822320	4822321	A	G	22	GENIC	homozygous	130032854
20	4822860	4822861	G	A	12	GENIC	homozygous	130032855
20	4823142	4823143	G		22	GENIC	homozygous	129979679
20	4819360	4819361	G	C	13	GENIC	homozygous	155140452