chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	36412244	36412245	A	T	21	GENIC	homozygous	116560817
10	36412667	36412668	C	T	23	GENIC	homozygous	116560819
10	36412786	36412787	C	T	21	GENIC	homozygous	116560821
10	36414072	36414073	T	C	32	GENIC	homozygous	116560823
10	36414565	36414566	G	A	19	GENIC	homozygous	116560825
10	36415183	36415184	A	G	17	GENIC	homozygous	116560827
10	36415218	36415219	T	A	17	GENIC	homozygous	116560829
10	36416061	36416062	G	A	26	GENIC	homozygous	116560831
10	36417347	36417348	T	C	12	GENIC	homozygous	116560833
10	36417361	36417362	G	A	12	GENIC	homozygous	116560835
10	36417547	36417548	C	T	14	GENIC	homozygous	116560843
10	36417638	36417639	A	G	25	GENIC	homozygous	116759151
10	36417643	36417644	G	A	29	GENIC	homozygous	116759153
10	36417676	36417677	G	T	24	GENIC	homozygous	116759155
10	36417716	36417717	T	C	26	GENIC	homozygous	116560845
10	36418679	36418680	T	C	13	GENIC	homozygous	116560847
10	36418681	36418682	C	T	14	GENIC	homozygous	116560849
10	36418944	36418945	C	T	25	GENIC	homozygous	116560851
10	36418955	36418956	T	C	21	GENIC	homozygous	116560853
10	36419080	36419081	C	A	13	GENIC	homozygous	116560855
10	36419305	36419306	C	G	16	GENIC	homozygous	116560857
10	36419306	36419307	A	G	16	GENIC	homozygous	116560859
10	36419408	36419409	T	C	14	GENIC	homozygous	116560861
10	36419481	36419482	T	C	14	GENIC	homozygous	116560863
10	36419708	36419709	G	A	14	GENIC	homozygous	116560865
10	36419878	36419879	C	T	20	GENIC	homozygous	116560867
10	36419968	36419969	A	G	24	GENIC	homozygous	116560869
10	36420079	36420080	A	G	31	GENIC	homozygous	116560871
10	36420689	36420690	G	A	21	GENIC	homozygous	116560873
10	36421766	36421767	G	A	19	GENIC	homozygous	116560875
10	36421953	36421954	A	G	11	GENIC	homozygous	116560877