chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	16770436	16770437	T	C	23	GENIC	homozygous	116738932
10	16771607	16771608	G	A	22	GENIC	homozygous	116738933
10	16772136	16772137	T	A	25	GENIC	homozygous	116499897
10	16774325	16774326	T	C	35	GENIC	homozygous	116499901
10	16774734	16774735	G	A	25	GENIC	homozygous	116738934
10	16775968	16775969	C	T	29	GENIC	homozygous	116738935
10	16776843	16776844	G	A	35	GENIC	homozygous	116738936
10	16778709	16778710	T	C	27	GENIC	homozygous	116499909
10	16779128	16779129	T	C	18	GENIC	homozygous	116738937
10	16780443	16780444	T	C	20	GENIC	homozygous	116738938
10	16781463	16781464	C	T	25	GENIC	possibly homozygous	116738939
10	16785279	16785280	A	G	30	GENIC	homozygous	116738940
10	16785301	16785302	G	A	28	GENIC	homozygous	116738941
10	16785321	16785322	T	C	20	GENIC	homozygous	116738942
10	16785521	16785522	C	T	41	GENIC	homozygous	116738943
10	16785536	16785537	T	C	36	GENIC	homozygous	116738944
10	16786037	16786038	C	T	27	GENIC	homozygous	116738945
10	16786140	16786141	A	G	25	GENIC	homozygous	116738946
10	16786452	16786453	A	G	19	GENIC	homozygous	116499919
10	16787154	16787155	G	A	25	GENIC	homozygous	116738947
10	16787443	16787444	T	C	28	GENIC	homozygous	116738951
10	16788319	16788320	T	C	18	GENIC	homozygous	116499921
10	16788954	16788955	A	C	28	GENIC	homozygous	116738952
10	16789312	16789313	T	C	26	GENIC	homozygous	116738953
10	16789645	16789646	C	T	25	GENIC	homozygous	116738954
10	16791471	16791472	A	C	29	GENIC	homozygous	116738956
10	16780160	16780161	T	G	24	GENIC	homozygous	116861029