chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	109620536	109620537	A	T	59	GENIC	homozygous	118054001
10	109621271	109621272	A	G	61	GENIC	homozygous	118054002
10	109621565	109621566	T	A	68	GENIC	homozygous	116718725
10	109622112	109622113	T	C	56	GENIC	homozygous	116718729
10	109622747	109622748	A	G	60	GENIC	homozygous	116718737
10	109622803	109622804	A	G	53	GENIC	homozygous	116718739
10	109623005	109623006	G	A	46	GENIC	possibly homozygous	116718741
10	109623669	109623670	G	A	46	GENIC	heterozygous	118054003
10	109623673	109623674	G	A	47	GENIC	possibly homozygous	118054004
10	109624580	109624581	A	G	62	GENIC	homozygous	116718743
10	109624600	109624601	C	T	63	GENIC	homozygous	116718745
10	109624800	109624801	T	G	58	GENIC	homozygous	116718747
10	109625094	109625095	G	A	75	GENIC	homozygous	116718749
10	109625173	109625174	G	T	65	GENIC	possibly homozygous	118054005
10	109624477	109624478	A	G	9	GENIC	homozygous	118013142