chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	10809159	10809160	T		13	GENIC	possibly homozygous	128789536
10	10809844	10809844		T	2	GENIC	homozygous	132142963
10	10810455	10810455		T	15	GENIC	homozygous	128789537
10	10812431	10812432	A	C	21	GENIC	homozygous	116858616
10	10813299	10813300	A	G	30	GENIC	homozygous	116493783
10	10814991	10814992	G	A	22	GENIC	homozygous	116493785
10	10815294	10815295	T	C	27	GENIC	homozygous	116493787
10	10816094	10816095	G	A	32	GENIC	homozygous	116858618
10	10816308	10816309	T	C	27	GENIC	homozygous	116493789
10	10817455	10817456	G	T	22	GENIC	homozygous	116493791
10	10817542	10817543	A	C	22	GENIC	homozygous	116493793
10	10817542	10817542		C	23	GENIC	homozygous	128789538
10	10817708	10817709	C	A	17	GENIC	homozygous	116493795
10	10818871	10818872	T	C	24	GENIC	homozygous	116734092
10	10821806	10821807	C	G	24	GENIC	homozygous	116858620
10	10822412	10822413	A	C	23	GENIC	homozygous	118079141
10	10823334	10823335	T	A	26	GENIC	homozygous	116734096
10	10823401	10823402	C		29	GENIC	homozygous	132142964
10	10823588	10823589	G	A	32	GENIC	homozygous	116493799
10	10824494	10824495	C	T	39	GENIC	homozygous	116858622
10	10826061	10826062	T	C	19	GENIC	homozygous	116734097
10	10826439	10826440	T	C	22	GENIC	homozygous	116858624
10	10826441	10826442	C	T	22	GENIC	homozygous	116493801
10	10827891	10827892	A	C	29	GENIC	homozygous	116858626
10	10829386	10829387	G	A	20	GENIC	homozygous	116858628