chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	109620956	109620957	C	G	42	GENIC	homozygous	116718721
10	109621176	109621177	C	T	43	GENIC	homozygous	116718723
10	109621565	109621566	T	A	41	GENIC	homozygous	116718725
10	109622042	109622043	T	G	49	GENIC	homozygous	116718727
10	109622112	109622113	T	C	35	GENIC	homozygous	116718729
10	109622187	109622188	C	T	41	GENIC	homozygous	116718731
10	109622202	109622203	G	T	42	GENIC	possibly homozygous	116718733
10	109622373	109622374	G	A	43	GENIC	homozygous	116718735
10	109622747	109622748	A	G	42	GENIC	homozygous	116718737
10	109622803	109622804	A	G	28	GENIC	homozygous	116718739
10	109623005	109623006	G	A	40	GENIC	homozygous	116718741
10	109624580	109624581	A	G	52	GENIC	homozygous	116718743
10	109624600	109624601	C	T	50	GENIC	homozygous	116718745
10	109624800	109624801	T	G	50	GENIC	homozygous	116718747
10	109625094	109625095	G	A	45	GENIC	homozygous	116718749