chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	61707382	61707383	A	G	17	GENIC	homozygous	116613020
10	61708979	61708980	T	C	14	GENIC	homozygous	116613024
10	61709047	61709048	T	C	20	GENIC	homozygous	116613026
10	61709380	61709381	T	A	13	GENIC	homozygous	116613028
10	61709435	61709436	C	A	13	GENIC	homozygous	116939451
10	61711498	61711499	G	T	8	GENIC	homozygous	116613032
10	61711525	61711526	A	T	8	GENIC	homozygous	116613034
10	61711918	61711919	C	A	10	GENIC	homozygous	116613036
10	61712130	61712131	A	C	26	GENIC	homozygous	116613038
10	61713247	61713248	T	C	21	GENIC	homozygous	116613040
10	61726736	61726737	G	C	23	GENIC	homozygous	116613045
10	61726817	61726818	A	T	24	GENIC	homozygous	116939453
10	61731923	61731924	C	G	24	GENIC	homozygous	126383720
10	61732017	61732018	T	G	17	GENIC	homozygous	126383721
10	61736021	61736022	G	A	10	GENIC	homozygous	116790709
10	61741962	61741963	C	T	15	GENIC	homozygous	116790711
10	61742990	61742991	A	T	23	GENIC	homozygous	116939455
10	61744810	61744811	C	A	9	GENIC	homozygous	116978441