chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	109620956	109620957	C	G	24	GENIC	homozygous	116718721
10	109621176	109621177	C	T	16	GENIC	possibly homozygous	116718723
10	109621565	109621566	T	A	23	GENIC	homozygous	116718725
10	109622042	109622043	T	G	27	GENIC	homozygous	116718727
10	109622112	109622113	T	C	17	GENIC	homozygous	116718729
10	109622187	109622188	C	T	25	GENIC	possibly homozygous	116718731
10	109622202	109622203	G	T	24	GENIC	possibly homozygous	116718733
10	109622373	109622374	G	A	31	GENIC	homozygous	116718735
10	109622747	109622748	A	G	34	GENIC	possibly homozygous	116718737
10	109622803	109622804	A	G	39	GENIC	possibly homozygous	116718739
10	109623005	109623006	G	A	31	GENIC	possibly homozygous	116718741
10	109623609	109623610	C	T	13	GENIC	homozygous	117136826
10	109624580	109624581	A	G	20	GENIC	homozygous	116718743
10	109624600	109624601	C	T	14	GENIC	homozygous	116718745
10	109624800	109624801	T	G	27	GENIC	possibly homozygous	116718747
10	109625094	109625095	G	A	31	GENIC	homozygous	116718749