chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	16772136	16772137	T	A	53	GENIC	homozygous	116499897
10	16773819	16773820	C	T	66	GENIC	homozygous	116499899
10	16774325	16774326	T	C	69	GENIC	homozygous	116499901
10	16775904	16775905	A	T	59	GENIC	homozygous	116499903
10	16778172	16778173	A	G	51	GENIC	homozygous	116499905
10	16778308	16778309	G	T	39	GENIC	homozygous	116499907
10	16778709	16778710	T	C	51	GENIC	homozygous	116499909
10	16779444	16779445	A	T	62	GENIC	homozygous	116499911
10	16780326	16780327	C	T	62	GENIC	homozygous	116499913
10	16781690	16781691	G	C	64	GENIC	homozygous	116499915
10	16785088	16785089	G	A	22	GENIC	homozygous	116499917
10	16786319	16786320	A	C	8	GENIC	heterozygous	128865668
10	16786320	16786321	A	C	8	GENIC	heterozygous	128865669
10	16786452	16786453	A	G	57	GENIC	homozygous	116499919
10	16788319	16788320	T	C	73	GENIC	homozygous	116499921
10	16789512	16789513	G	A	69	GENIC	possibly homozygous	116499923
10	16790085	16790086	T	C	60	GENIC	homozygous	116499925
10	16792383	16792384	C	T	56	GENIC	homozygous	116499927
10	16786347	16786348	C		22	GENIC	homozygous	128791580
10	16787678	16787678		CCC	8	GENIC	homozygous	128791581
10	16790294	16790295	A		57	GENIC	homozygous	128791582