chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	5594899	5594899		TTTG	30	GENIC	possibly homozygous	128568458
8	5598808	5598809	T	G	56	GENIC	homozygous	116425397
8	5597001	5597002	T	G	57	GENIC	homozygous	116425395
8	5597715	5597716	C	T	58	GENIC	homozygous	116425396
8	5598917	5598918	T	C	80	GENIC	homozygous	116425398
8	5599708	5599709	A		52	GENIC	homozygous	128568459
8	5601319	5601320	G	A	50	GENIC	homozygous	116425399
8	5601713	5601714	T	C	54	GENIC	homozygous	116425400
8	5602008	5602009	T	G	53	GENIC	homozygous	116425401
8	5602047	5602048	G	C	49	GENIC	homozygous	116425402
8	5603640	5603641	T	C	52	GENIC	homozygous	116425403
8	5605268	5605269	C	A	56	GENIC	homozygous	116425404
8	5605580	5605581	A	G	48	GENIC	homozygous	116425405
8	5612004	5612005	C	T	46	GENIC	homozygous	116425406
8	5613419	5613420	A	T	61	GENIC	homozygous	116425407
8	5613420	5613421	G	T	59	GENIC	homozygous	116425408
8	5615623	5615624	A	G	59	GENIC	homozygous	116425409