chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	16770417	16770418	C	T	34	GENIC	homozygous	116994870
10	16772136	16772137	T	A	36	GENIC	homozygous	116499897
10	16772298	16772299	T	G	24	GENIC	homozygous	116994871
10	16774325	16774326	T	C	29	GENIC	homozygous	116499901
10	16775193	16775194	C	T	34	GENIC	homozygous	116994872
10	16778171	16778172	G	A	26	GENIC	homozygous	116994873
10	16778709	16778710	T	C	27	GENIC	homozygous	116499909
10	16779215	16779216	C	T	18	GENIC	homozygous	116994874
10	16779855	16779856	G	A	27	GENIC	homozygous	116994875
10	16780443	16780444	T	C	29	GENIC	homozygous	116738938
10	16781463	16781464	C	T	34	GENIC	homozygous	116738939
10	16785279	16785280	A	G	33	GENIC	homozygous	116738940
10	16785301	16785302	G	A	30	GENIC	homozygous	116738941
10	16785321	16785322	T	C	29	GENIC	homozygous	116738942
10	16785485	16785486	C	G	35	GENIC	homozygous	116994876
10	16785521	16785522	C	T	35	GENIC	homozygous	116738943
10	16785536	16785537	T	C	28	GENIC	homozygous	116738944
10	16786037	16786038	C	T	23	GENIC	homozygous	116738945
10	16786140	16786141	A	G	33	GENIC	homozygous	116738946
10	16786452	16786453	A	G	40	GENIC	homozygous	116499919
10	16787443	16787444	T	C	24	GENIC	homozygous	116738951
10	16788319	16788320	T	C	18	GENIC	homozygous	116499921
10	16788954	16788955	A	C	40	GENIC	homozygous	116738952
10	16789312	16789313	T	C	31	GENIC	homozygous	116738953
10	16789808	16789809	G	T	52	GENIC	homozygous	116738955
10	16791471	16791472	A	C	30	GENIC	homozygous	116738956
10	16780160	16780161	T	G	25	GENIC	homozygous	116861029
10	16789112	16789113	A	C	39	GENIC	homozygous	116861031