chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	3518560	3518561	G	A	55	GENIC	possibly homozygous	114706909
6	3518573	3518574	T	C	50	GENIC	homozygous	114706910
6	3518576	3518577	T	G	51	GENIC	homozygous	114706911
6	3519391	3519392	C	G	51	GENIC	homozygous	114706912
6	3519657	3519658	A	G	39	GENIC	possibly homozygous	114706913
6	3519689	3519690	G	C	40	GENIC	possibly homozygous	114706914
6	3519846	3519847	T	C	44	GENIC	homozygous	115037150
6	3519913	3519914	C	T	55	GENIC	homozygous	115037151
6	3520993	3520994	T	C	63	GENIC	homozygous	114706915
6	3521222	3521223	G	A	81	GENIC	homozygous	114706916
6	3521476	3521477	T	C	47	GENIC	homozygous	114706917
6	3521550	3521551	C	T	45	GENIC	homozygous	114706918
6	3521587	3521588	T	C	48	GENIC	homozygous	114706919
6	3521990	3521991	T	C	64	GENIC	homozygous	114706920
6	3522071	3522072	A	G	62	GENIC	homozygous	114706921
6	3522172	3522173	A	C	49	GENIC	homozygous	114706923
6	3522247	3522248	T	C	55	GENIC	homozygous	114706924
6	3522413	3522414	T	A	55	GENIC	homozygous	114706925