chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	2918221	2918222	T	C	44	GENIC	homozygous	130017525
20	2918433	2918434	A	T	53	GENIC	homozygous	130017526
20	2918519	2918520	G	T	47	GENIC	homozygous	130017527
20	2918639	2918643	TCTG		36	GENIC	homozygous	129976595
20	2918802	2918803	C	T	54	GENIC	homozygous	130017528
20	2918936	2918940	TTTA		39	GENIC	homozygous	129976596
20	2918943	2918944	A	T	40	GENIC	homozygous	130017529
20	2918971	2918982	ATCTATCTATC		41	GENIC	homozygous	129976597
20	2919020	2919021	A	G	43	GENIC	homozygous	130017530
20	2919069	2919070	T	C	40	GENIC	homozygous	130017531
20	2919438	2919439	G	T	41	GENIC	homozygous	130017532
20	2919666	2919667	A	G	34	GENIC	homozygous	130017533
20	2919706	2919706		G	22	GENIC	possibly homozygous	129976598
20	2920312	2920313	T	A	52	GENIC	homozygous	130017534
20	2920313	2920314	C	T	53	GENIC	homozygous	130017535
20	2920455	2920456	G	A	51	GENIC	homozygous	130017536
20	2924019	2924019		GT	9	GENIC	heterozygous	129976599