chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	38459948	38459949	T	C	23	GENIC	homozygous	115322968
12	38459959	38459960	G	A	28	GENIC	homozygous	115322970
12	38460114	38460115	A	C	43	GENIC	homozygous	115382561
12	38461239	38461240	G	A	41	GENIC	homozygous	115322972
12	38461327	38461328	A	G	57	GENIC	homozygous	115322974
12	38461661	38461662	A	G	61	GENIC	homozygous	115322976
12	38462749	38462750	T	A	15	GENIC	homozygous	118269949
12	38462860	38462861	T	A	42	GENIC	homozygous	115382563
12	38462881	38462882	A	C	52	GENIC	homozygous	115382565
12	38462890	38462891	G	A	57	GENIC	homozygous	115382567
12	38462968	38462969	T	A	53	GENIC	homozygous	115322978
12	38462993	38462994	T	A	54	GENIC	homozygous	115322980
12	38463194	38463195	G	T	35	GENIC	possibly homozygous	118337996
12	38466652	38466653	C	A	19	GENIC	possibly homozygous	118337997
12	38466989	38466990	A	T	35	GENIC	homozygous	115323008
12	38467048	38467049	T	C	39	GENIC	possibly homozygous	115323010
12	38471461	38471462	G	T	15	GENIC	homozygous	118269959
12	38471510	38471511	C	A	16	GENIC	possibly homozygous	118269960
12	38472509	38472510	G	A	41	GENIC	possibly homozygous	115382569
12	38475630	38475631	G	C	17	GENIC	homozygous	115521610
12	38476560	38476561	C	G	48	GENIC	possibly homozygous	115440517
12	38476562	38476563	C	G	47	GENIC	homozygous	115440518
12	38482891	38482892	C	T	35	GENIC	homozygous	115323095
12	38482899	38482900	A	C	35	GENIC	homozygous	115323097
12	38466813	38466814	A	G	45	GENIC	homozygous	115451262