chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	13914688	13914689	T	C	26	GENIC	homozygous	115445263
12	13919559	13919560	T	G	52	GENIC	homozygous	115261755
12	13915612	13915612		C	20	GENIC	possibly homozygous	128962308
12	13918113	13918114	T	C	60	GENIC	homozygous	115261751
12	13919442	13919443	T	A	48	GENIC	homozygous	115261753
12	13919769	13919770	C	T	55	GENIC	homozygous	115261757
12	13921810	13921811	C	T	45	GENIC	homozygous	115261759
12	13923107	13923108	A	G	53	GENIC	homozygous	115261761
12	13923112	13923113	A	G	52	GENIC	homozygous	115261763
12	13923439	13923440	T	C	51	GENIC	homozygous	115261765
12	13924028	13924029	G	A	65	GENIC	possibly homozygous	115261767
12	13923513	13923514	T	C	57	GENIC	homozygous	115437965