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	21	GENIC	homozygous	115322970
12	38461239	38461240	G	A	31	GENIC	homozygous	115322972
12	38461327	38461328	A	G	37	GENIC	homozygous	115322974
12	38461661	38461662	A	G	39	GENIC	homozygous	115322976
12	38462749	38462750	T	A	16	GENIC	homozygous	118269949
12	38462860	38462861	T	A	30	GENIC	homozygous	115382563
12	38462881	38462882	A	C	32	GENIC	homozygous	115382565
12	38462890	38462891	G	A	33	GENIC	homozygous	115382567
12	38462968	38462969	T	A	34	GENIC	homozygous	115322978
12	38462993	38462994	T	A	36	GENIC	homozygous	115322980
12	38466813	38466814	A	G	30	GENIC	homozygous	115451262
12	38466989	38466990	A	T	26	GENIC	homozygous	115323008
12	38467048	38467049	T	C	44	GENIC	homozygous	115323010
12	38471461	38471462	G	T	15	GENIC	homozygous	118269959
12	38471510	38471511	C	A	21	GENIC	possibly homozygous	118269960
12	38476560	38476561	C	G	34	GENIC	homozygous	115440517
12	38476562	38476563	C	G	34	GENIC	homozygous	115440518
12	38475562	38475563	G	A	11	GENIC	homozygous	118343066
12	38475547	38475548	G	C	13	GENIC	homozygous	118343065