chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	210445791	210445792	A	G	39	GENIC	homozygous	57071432
4	210446380	210446381	C	T	37	GENIC	homozygous	57071433
4	210446416	210446417	G	A	41	GENIC	homozygous	57071434
4	210446965	210446967	CC	--	4	GENIC	homozygous	57071435
4	210446981	210446982	T	C	8	GENIC	homozygous	57071436
4	210446985	210446986	T	C	8	GENIC	homozygous	57071437
4	210446989	210446990	T	C	10	GENIC	homozygous	57071438
4	210448345	210448346	C	T	31	GENIC	homozygous	57071440
4	210448398	210448399	G	GC	13	GENIC	homozygous	57071441
4	210450150	210450151	G	GCATCCATC	12	GENIC	homozygous	57071442
4	210450441	210450442	C	T	37	GENIC	homozygous	57071443
4	210450494	210450495	G	A	41	GENIC	homozygous	57071444
4	210450985	210450986	T	A	53	GENIC	homozygous	57071445
4	210452183	210452184	T	A	39	GENIC	homozygous	57071446