chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	97214124	97214125	C	T	25	GENIC	homozygous	117180669
10	97214609	97214610	T	C	37	GENIC	homozygous	117180670
10	97216014	97216015	C	G	24	GENIC	homozygous	116693171
10	97216410	97216411	A	G	28	GENIC	homozygous	116693173
10	97218563	97218564	T	A	30	GENIC	homozygous	117180671
10	97218845	97218846	C	T	28	GENIC	homozygous	117180672
10	97220793	97220794	C	T	24	GENIC	possibly homozygous	117180673
10	97223109	97223110	T	C	26	GENIC	homozygous	116693175
10	97225239	97225240	T	C	28	GENIC	homozygous	117180674
10	97230587	97230588	C	T	21	GENIC	homozygous	117180675
10	97230708	97230709	A	G	14	GENIC	homozygous	116693181
10	97230845	97230846	G	A	20	GENIC	homozygous	117180676
10	97230922	97230923	C	A	23	GENIC	homozygous	117180677
10	97231082	97231083	G	A	12	GENIC	homozygous	117180678
10	97231355	97231356	C	T	21	GENIC	homozygous	117180679
10	97231670	97231671	T	C	15	GENIC	homozygous	116693183
10	97233031	97233032	C	T	28	GENIC	homozygous	117180680
10	97233609	97233610	C	T	39	GENIC	homozygous	117180681
10	97233681	97233682	C	T	36	GENIC	homozygous	117180682
10	97234089	97234090	T	C	26	GENIC	homozygous	116956260
10	97235326	97235327	T	C	20	GENIC	homozygous	116956264
10	97236200	97236201	C	T	14	GENIC	homozygous	117180683
10	97236529	97236530	C	G	21	GENIC	homozygous	116693189
10	97236746	97236747	C	T	21	GENIC	possibly homozygous	117180684
10	97236994	97236995	A	G	26	GENIC	possibly homozygous	117180685
10	97237327	97237328	G	T	22	GENIC	homozygous	117180686
10	97237330	97237331	T	C	21	GENIC	homozygous	117180687
10	97237417	97237418	T	C	23	GENIC	homozygous	116693191
10	97238245	97238246	C	T	12	GENIC	homozygous	117180688
10	97238291	97238292	C	T	13	GENIC	possibly homozygous	117180689
10	97238430	97238431	C	T	14	GENIC	possibly homozygous	117180690